- Research article
- Open Access
Homeotic transformations reflect departure from the mammalian ‘rule of seven’ cervical vertebrae in sloths: inferences on the Hox code and morphological modularity of the mammalian neck
BMC Evolutionary Biology volume 18, Article number: 84 (2018)
Sloths are one of only two exceptions to the mammalian ‘rule of seven’ vertebrae in the neck. As a striking case of breaking the evolutionary constraint, the explanation for the exceptional number of cervical vertebrae in sloths is still under debate. Two diverging hypotheses, both ultimately linked to the low metabolic rate of sloths, have been proposed: hypothesis 1 involves morphological transformation of vertebrae due to changes in the Hox gene expression pattern and hypothesis 2 assumes that the Hox gene expression pattern is not altered and the identity of the vertebrae is not changed. Direct evidence supporting either hypothesis would involve knowledge of the vertebral Hox code in sloths, but the realization of such studies is extremely limited. Here, on the basis of the previously established correlation between anterior Hox gene expression and the quantifiable vertebral shape, we present the morphological regionalization of the neck in three different species of sloths with aberrant cervical count providing indirect insight into the vertebral Hox code.
Shape differences within the cervical vertebral column suggest a mouse-like Hox code in the neck of sloths. We infer an anterior shift of HoxC-6 expression in association with the first thoracic vertebra in short-necked sloths with decreased cervical count, and a posterior shift of HoxC-5 and HoxC-6 expression in long-necked sloths with increased cervical count.
Although only future developmental analyses in non-model organisms, such as sloths, will yield direct evidence for the evolutionary mechanism responsible for the aberrant number of cervical vertebrae, our observations lend support to hypothesis 1 indicating that the number of modules is retained but their boundaries are displaced. Our approach based on quantified morphological differences also provides a reliable basis for further research including fossil taxa such as extinct ‘ground sloths’ in order to trace the pattern and the underlying genetic mechanisms in the evolution of the vertebral column in mammals.
The mammalian ‘rule of seven’ vertebrae in the neck is a striking case of evolutionary stasis [1,2,3]. In contrast to non-mammalian amniotes, mammals are highly constrained in the number of cervical vertebrae (CV) and their neck kinematics rely on interspecific variation in vertebral morphology, but not in vertebral count [4, 5]. The developmental origin of this meristic constraint in the mammalian neck, however, is still under debate [2, 6, 7]. One explanation posits that numerical changes in cervical count may be coupled with indirect selection due to pleiotropy (e.g., [8,9,10]). Pleiotropy refers to the phenomenon of mutations in a single gene that affect more than one phenotypic character of an organism [10,11,12]. Changes in pleiotropic genes were found to be associated with effects that dramatically lower fitness (malformations and cancers), and thus may indirectly constrain evolutionary change through stabilizing selection (e.g., [8, 11, 13]). Indeed, skeletons of mammals with an atypical number of CV show many anomalies, such as fusion of vertebrae, defective production of cartilage, abnormal ossification of sternum and pelvic girdle, abnormal fibrous bands connected to rudimentary ribs, and asymmetric ribs [2, 14, 15]. A further explanation states that the meristic constraint arose as a byproduct of the origin of the muscularization of the mammalian diaphragm [6, 7]. The migrating muscle precursor (MMP) cells that form the diaphragm originate from the midcervical somites and migrate posteriorly . Both an anterior and posterior transposition of the forelimb (resulting in less or more cervicals, respectively) are likely to generate a deficiency in the development of the muscularized diaphragm, of the forelimb, or both . This specialization of the midcervical somites associated with the MMP cells responsible for the developing mammalian diaphragm became again subject to stabilizing selection after its first appearance in the Triassic .
Recent work revealed a correlation between anterior Hox gene expression and the quantifiable shape of the CV in living archosaurs . Although differing in the number of cervical vertebrae, birds and crocodiles share a common underlying Hox gene modularity. Following this, changes in the expression of the underlying genetic code can be hypothesized solely from quantifiable vertebral morphology (e.g., for fossils with known cervical morphology, (see )). A similar correlation and modularity was subsequently shown for the mammalian model species mouse , the only mammal for which the Hox gene expression patterns have been established [18, 19]. Three morphological subunits were detected in the postatlantal cervical vertebral column of the mouse indicating that two distinct shape changes occur between successive CV (between C2 and C3 and between C5 and C6) . This morphological modularity detected in the mouse appears to represent the general pattern for living mammals with seven CV [6, 17, 20] with overall cervical spine length as the main source of variation in the mammalian neck . A conservative complex of C3–5 responsible for the development of the muscularized diaphragm  is in line with this observed modularity in the mouse. Although phylogenetically diverse, there is evidence for a common Hox code in living placental mammals as they appear to display similar patterns of morphological differentiation within the neck, which is thought to reflect a common developmental regionalization [6, 22]. It was suggested that this pattern might even be valid for all synapsids (with seven CV) . In order to have a similar validation as in archosaurs, however, morphological-developmental patterns in mammals with different numbers of vertebrae have to be examined. Differences in the number of vertebrae with cervical identity would imply a morphological regionalization of the neck that corresponds to modifications in Hox gene expression domains (expansion of a Hox gene’s expression domain and/or a shift of gene expression) [16, 23].
Besides manatees (Sirenia), sloths (Xenarthra) are the only mammals departing from the mammalian ‘rule of seven’ vertebrae in the neck. They display either reduced or increased cervical counts and show considerable intraspecific variation in the number of CV [1,2,3, 15, 24,25,26,27]. Consequently, analyses of these exceptions were conducted to further our understanding of the evolutionary conservatism in the mammalian axial skeleton which is also the objective of the present study. The two living, distantly related genera of sloths (belonging to the Megalonychidae and Bradypodidae) are superficially similar (folivorous, arboreal, upside-down posture, suspensory locomotion) , but two-toed sloths (Choloepus) have five to eight CV while three-toed sloths (Bradypus) have eight to ten CV [3, 15, 26, 29, 30]. Choloepus usually has a relatively short and robust neck and keeps its head upside-down during suspensory postures. Bradypus, in contrast, has a remarkably long and flexible neck and is reported to be able to rotate its head for 270° in both directions [31, 32]. Like the developmental origin of the mammalian ‘rule of seven’ CV (see above), the explanation for the exceptional number of CV in sloths is still under debate [2, 15, 24,25,26,27], yet a mechanism that allows sloths to depart from this ‘rule’ is clearly involved.
There are two hypotheses for the breaking of the meristic constraint underlying the aberrant vertebral count in the sloths’ neck compared to the previously described mouse pattern: (1) The number of modules is retained but their boundaries are displaced and (2) the number of modules is altered but their boundaries are retained (Fig. 1). For both hypotheses, seemingly diverging but not mutually exclusive evidences from development have been provided (see below). The first hypothesis assumes changes in the Hox gene expression pattern that result in the morphological transformation of vertebrae (i.e., homeosis) [1, 2, 14, 15]. A shorter neck, according to the homeosis hypothesis, is associated with homeotic transformation of CV into thoracic vertebrae, whereas a longer neck is the result of homeotic transformation of thoracic vertebrae into CV. Despite the pleiotropic effects described above, low metabolic rates in sloths were proposed to result in relaxed selection regimes [2, 8, 15, 33]. The concept of homeosis, however, is here not applied in the strict definition of Bateson , which implies local shifts of individual serial elements while the others remain unchanged (e.g., C7 anatomy is replaced by thoracic vertebra 1 anatomy in Choloepus specimens with six CV). We rather understand homeosis here as global developmental changes sensu Buchholtz & Wayrynen (2014) . These global changes involve displacements of boundaries between axial regions but with the full range of cervical anatomies still present and thus a dissociation of axial patterning and segmentation .
The second hypothesis assumes that the Hox gene expression pattern is not altered and the identity of the vertebrae is not changed [7, 26, 27, 31]. This involves a level of independence of components of the axial skeleton derived from somitic vs. those derived from lateral plate mesoderm (primaxial/abaxial repatterning, PAR). Again, this does not exclude a role for stabilizing selection [26, 27]. Accordingly, the number of CV and the modular boundaries remain the same, but a shift of the abaxial elements (pectoral girdle and limbs) occurred relative to the adjacent and stationary primaxial domain (vertebrae) resulting in shorter and longer necks, respectively. Indeed, the vertebral ossification pattern indicates that the posterior CV in the long-necked sloths (Bradypus) are developmentally thoracic . Importantly, this second hypothesis, as the first one, assumes that the extremely low metabolic rates of sloths allow for their apparent tolerance to unusual cervical counts . Furthermore, both hypotheses are consistent with a diaphragm-linked origin of the cervical constraint .
The present study takes advantage of the recent work that revealed the correlation between anterior Hox gene expression patterns and the quantifiable shape of the CV [16, 17] to gain insight into the aberrant cervical count in sloths. We used three-dimensional (3D) geometric morphometrics combined with a relative warps analysis (see methods) to quantify shape differences between species (interspecific dataset) and within the cervical series of each specimen (intraspecific dataset) separately. Since hypothesis 1 predicts that the number of vertebrae with cervical identity is changed, whereas hypothesis 2 predicts that the first seven vertebrae retain cervical identity, we here test (1) whether the morphological pattern of sloths with seven CV corresponds to the postulated general modularity pattern of living mammals (i.e., the three-subunit pattern); (2) whether the morphological pattern of sloths with more or less than seven CV indicates a change in the number of vertebrae with cervical identity; and (3) whether the alteration in the number of CV is accompanied by a displacement of boundaries between modules. This will help to further elucidate the evolutionary mechanism behind the conservatism of cervical count in mammals and its departure in sloths.
The landmark-based 3D geometric morphometric analysis of the interspecific data set (including all CV of the four specimens together) showed that Choloepus and Bradypus occupy distinct regions of the morphospace (Fig. 2). Bradypus variegatus and B. tridactylus cluster together, whereas the C. cf. didactylus 1 and C. didactylus 2 do so as well, but show less overlap. In all analyzed sloths, C2 is very distinct in its morphology and is separate from the postaxial vertebrae.
The intraneck data set (treating each specimen separately) revealed a distinct morphological differentiation of the neck in all analyzed sloths (Fig. 3a-d). At least 80% of the total variance in the sample is explained by the first two relative warps (Additional file 1: Table S1) and, thus, the morphospace constructed from relative warp 1 and relative warp 2 provides a reasonable approximation of the total shape variation. Relative warp 1 separates C2 from the postaxial vertebrae in each taxon whereas relative warp 2 separates the postaxial vertebrae into an anterior and a posterior group (Fig. 3). The posterior group comprises the last cervical vertebra in C. cf. didactylus 1, C. didactylus 2, and B. variegatus, but the last two CV in B. tridactylus.
As confirmed by the cluster analysis (Additional file 1: Figure S1), the relative warps analysis allowed discrimination of the vertebrae. In all sloths analyzed, the geometric morphometric analysis revealed a three-subunit pattern (Fig. 3e). The common modular pattern comprises the axis (C2), an anterior, and a posterior unit. The distribution of the CV onto the specific modules, however, reveals variation among species. In C. cf. didactylus 1 (six CV), the modular pattern includes C2, three anterior (C3–5), and one posterior (C6) vertebrae. Including the first thoracic vertebra (V7 in this specimen) in the morphometric analyses confirmed that it is very distinct in its morphology (not shown here), as it does not cluster with C6. In C. didactylus 2 (seven CV), the morphological subunits comprise C2, four anterior CV (C3–6), and one posterior (C7) cervical vertebra. The morphological subunits of both long-necked sloths (nine CV), B. variegatus and B. tridactylus, comprised C2, six anterior CV (C3–8) and one posterior (C9) cervical vertebra. Examples of congenital anomalies were found in all specimens (Fig. 4, Additional file 1: Figure S2).
Qualitative vs. quantitative morphology
The modular pattern in sloths as quantified by the present morphological analysis is in agreement with the extensive qualitative survey of vertebral morphology by Varela-Lasheras et al. (2011) . The first five or six CV of Choloepus and the first eight CV of Bradypus have an unambiguous cervical shape , which corresponds to the atlas, axis, and the anterior morphological subunit (this study). The last vertebra (C6, 7, and 9, respectively) in the neck always had a transient cervicothoracic shape and rudimentary ribs , which corresponds to the posterior morphological subunit (this study). Furthermore, Varela-Lasheras et al. (2011)  observed that the penultimate vertebra in the neck of Bradypus (C8) had a transitional cervicothoracic shape in two specimens. Indeed, the modular pattern of B. variegatus and B. tridactylus differs in our study in regard of the assignment of C8 to the anterior or posterior morphological subunit (Fig. 3c, d). A study of morphological modularity in the vertebral column of modern cats (Felidae) correspondingly revealed a transitional module comprising the last two CV and the first two thoracic vertebrae (C6-T2) .
Sloths with seven CV and the postulated general pattern of living mammals
The morphological three-subunit pattern found in the neck of the mouse is viewed as representing the general pattern for living mammals with seven CV [6, 17, 20]. Two distinct shape changes occur in the post-atlantal cervical series between successive CV: between C2–3 and between C5–6 . The present study detected a corresponding modular, three-subunit pattern for C. didactylus 2 (seven CV), but the distinct shape change in the posterior part of the neck occurs between C6–7 rather than between C5–6. On the basis of the correlation between anterior Hox gene expression and quantifiable vertebral shape of the CV in the mouse, this could possibly be the result of the expression of HoxC-5 being shifted posteriorly by one vertebra in C. didactylus 2. Thus, the number of modules in the neck of the sloth with seven CV is the same as for the mouse, but the boundary between the anterior and posterior module is shifted.
Morphological specialization to the suspensory lifestyle of sloths may contribute to the difference in their modular pattern. The CV form a mobile, multi-jointed structure with complex kinematics and requiring the coordination of many muscles [36,37,38]. A reduction of this complexity could be achieved by the regionalization of the cervical vertebral column [20, 39,40,41,42,43,44]. The functionally specialized vertebrae form three compartments and such a reduced geometry was suggested to facilitate motor control of the neck [39, 40]. Normally, the cervicothoracic transition involves the last two CV (C6–7), but it appears to be reduced in sloths involving only the last vertebra in the neck. This may again be linked to morpho-functional aspects of their cervical vertebral column. It has been shown in the giraffe that the attachment area of a neck flexor muscle (Musculus longus colli) is shifted posteriorly, which was interpreted as providing more flexibility to the neck . Suggesting a similar close relationship for the axial musculoskeletal system of sloths, the highly specialized locomotor mode of Choloepus is reflected in the intramuscular architecture of their dorsovertebral muscles [46, 47]. In terms of shoulder muscles, the development of the serratus ventralis and the rhomboideus may be linked to the posterior subunit in the neck of sloths. Parts of both muscles originate from the posterior CV and insert on the scapula [48, 49]. In general, the main function of these muscles is suspension of the thorax between the forelimbs. Due to the inverse body orientation in sloths, however, they are not suited to fulfill this role . Correspondingly, these muscles are weakly developed or even absent [32, 48, 50]. This may entail that the posterior subunit comprises only the last vertebra instead of the last two CV as in the mouse.
Sloths with a decreased number of CV
The modular pattern in the cervical vertebral column of C. cf. didactylus 1 (six CV) corresponds to the pattern detected in the neck of C. didactylus 2 (seven CV), but is shifted by one vertebra since the neck is shorter. Thus, the hypothesis 1 (same number of modules, displacement of module boundaries) is favored. The distinct shape change in the posterior part of the cervical vertebral column occurs between the two last vertebrae (C5–6). This suggests that the anterior expression limit of HoxC-5 is similar to that of the mouse at C6, but the seventh vertebra appears to be homeotically transformed into a thoracic vertebra in the sloth. However, since the complete range of vertebral morphologies is present (Fig. 4; C6 resembles C7 in C. didactylus 2), the homeotic transformation is global rather than local (see ). More specifically, this indicates that the anterior expression limit of HoxC-6 is shifted anteriorly by one vertebra in C. cf. didactylus 1. It has been shown that the expression of the HoxC-6 gene starts at the first thoracic vertebra in a variety of amniotes that differ in cervical count [19, 23, 51]. It corresponds to the transition from cervical to thoracic vertebrae (i.e., cervicothoracic transition) in the mouse (seven CV), chicken (14 CV), goose (17 CV), crocodile (nine CV) and turtle (eight CV) [19, 23, 51]. A similar modular pattern as observed here in the cervical vertebral column of Choloepus has been reported for manatees (genus Trichechus) . The reduction in cervical count in Trichechus from seven to six resembles a similar global homeotic shift based on a global dissociation of the processes of somitogenesis and axial patterning . It thus further highlights the global validity of the modular pattern of the neck observed here.
Congenital anomalies (e.g., asymmetric vertebrae or vertebrae with rudimentary ribs) were found in all specimens including C. cf. didactylus 1 (Fig. 4a, Additional file 1: Figure S2) and have also previously been reported [15, 26]. Such transitional vertebral identities may be the result of Hox gene mutations and pleiotropic effects and hint at homeotic transformations . However, such morphologies have also been argued to be consistent with shifts between primaxially (i.e., of somitic origin) and abaxially (i.e., originating from lateral plate mesoderm) derived tissues in line with the primaxial/abaxial repatterning (PAR) hypothesis . It is also important to point out, in this context, that the patterning of the mesoderm plate is not collinear .
Sloths with an increased number of CV
The two Bradypus specimens studied here had more than seven CV, but still displayed a morphological three-subunit pattern in the neck corresponding to the general mammalian pattern. This results in a large anterior morphological subunit comprising five vertebrae in one individual and six vertebrae in the other individual (Fig. 3e). Correlated with the relative position of the posterior subunit, this indicates again that the number of modules is retained but the boundaries between them are displaced (hypothesis 1). The displacement is likely based on a posterior shift of HoxC-5 and HoxC-6 expression in the long-necked sloths. The difference in the assignment of C8 to the anterior (in B. variegatus) or posterior (in B. tridactylus) morphological subunit may suggest either a functional difference or interspecific variation. Since both species do not distinctly differ in behavior and are phylogenetically very close [53, 54], it seems more likely that this part of the neck is subject to interspecific variation.
The last two CV (C8–9) in long-necked sloths are the only vertebrae in the neck whose centra ossify before other cervical centra and neural arches . This observation was taken as evidence supporting an underlying PAR because the early ossification of C8–9 resembles the anterior-most rib-bearing thoracic vertebrae of other mammals  (note that this inference was also critized ). Therefore, the number of vertebrae with a cervical identity was interpreted as unchanged in Bradypus and it was inferred that no changes occurred in the Hox code . Although the complete range of vertebral morphologies is ‘stretched’ to eight or nine vertebrae, respectively (Fig. 3), it is not possible to exclude this possibility without any further genetic data. However, a complex, integrated network of signaling pathways and gene regulators governs bone formation and these molecular mechanisms are not independent of Hox gene activity .
Cervical ribs and HoxA-5
In contrast to vertebrae, which develop solely from the somitic mesoderm, the ribs derive from both somitic and lateral plate mesoderm [52, 56, 57]. Only the distalmost part of the rib (sternal rib) depends on the lateral plate mesoderm and is considered to be an abaxial element [52, 56, 57]. The rib head, neck, tubercle, and proximal part of the body of the rib derive from the somitic mesoderm and are considered axial elements [56, 57]. Following the PAR hypothesis, this suggests a shift between vertebrae including the proximal part of the ribs (primaxial structures) and the distalmost part of the ribs (abaxial structures) . Although the present results indicate homeotic transformations of the vertebrae in sloths with aberrant number of CV, the PAR hypothesis cannot be fully rejected in short-necked sloths since the sternal ribs are indeed shifted anteriorly. For long-necked sloths, the PAR hypothesis appears not to be supported because the increase in the number of CV is also associated with the loss of cervical ribs. However, considering that the increase in cervical count is also associated with a shift of the pelvis , none of the hypotheses can explain axial anatomy in Bradypus alone and parallel processes might be involved.
Several studies reported on the association between the development of cervical ribs and the expression of HoxA-5 in amniotes [16, 17, 23, 51, 52, 58,59,60]. Alligators and crocodiles possess free cervical ribs and the expression limit of HoxA-5 starts in the posterior cervical vertebral column [16, 23, 58]. In birds, whose cervical ribs are present, but fused to the vertebrae, the anterior expression limit of HoxA-5 is in the middle region of the neck  and HoxA-5 knockdown results in defects of the cervical ribs . This contrasts with the more anterior HoxA-5 expression observed in the mouse . The loss of free ribs on the CV (by reduction and fusion) in Mammaliaformes during the Cretaceous [6, 61,62,63], suggests that the anterior expression limit of HoxA-5 is shifted, hence resembling the pattern of the mouse . Since the CV in sloths often bear irregular fused riblets, it may be possible that HoxA-5 expression starts in the posterior region of the neck. It is not likely that a shift of the anterior expression limit of HoxA-5 occurred twice within one lineage, hence this may indicate that either the lineage towards modern sloths retained a posterior HoxA-5 expression, or the shift is a side-effect of the change in the expression of other Hox genes, in particular HoxC-5 and HoxC-6. Future studies are required to further elucidate the evolutionary role of HoxA-5 in axial patterning. Furthermore, the determination of the Hox gene inventory for sloths by PCR (polymerase chain reaction) survey would be a first crucial step in order to validate for the presence of Hox genes in comparison with other mammals.
Is the mammalian ‘rule of seven’ actually a ‘rule of three’?
Our morphological findings of the CV of sloths and the inferred Hox gene expression patterns support the hypothesis that the number of modules in the neck is retained but the borders between the modules are displaced when the cervical count is altered (hypothesis 1). Similar results were obtained for Trichechus, the only other mammalian genus with an aberrant number of CV . Thus, the general validity of the three-subunit pattern of the mouse  is confirmed even under varying vertebral number. However, the underlying developmental basis for the meristic variation in sloths cannot be clarified by our morphological approach as neither global homeotic changes nor PAR alone can explain all aspects of sloth skeletal anatomy. It is likely that different processes act in Choloepus and Bradypus or, as they are not mutually exclusive (see above), that parallel processes shape the overall anatomy of sloths necks (see ). Nevertheless, it becomes evident that the mammalian neck is not constrained to seven CV per se, but to the conserved modularity of underlying Hox gene expression dividing the neck into three subunits. As most amniote lineages, synapsids increased the number of cervical vertebrae from six (basic amniote pattern) to seven in therapsids resulting in increased head mobility . Further meristic variation, however, was prevented by strong developmental constraints based on the conserved Hox gene pattern since the Jurassic [2, 6]. Thus, the limitation to the number of seven CV is a byproduct of the arrested increase of cervical count. Nevertheless, variation in cervical number is not completely repressed as demonstrated by the sloths (and also the manatee). The three-subunit pattern, in contrast, seems not to be changeable even for those aberrant mammals.
Remarkably, sloths display variation in the number of CV, but a three-subunit morphological pattern in the neck is conserved - a pattern that appears to be common for mammals in general. In contrast to archosaurs (cf. [16, 23]), the correlation between anterior Hox gene expression and quantifiable shape of the CV found in sloths with aberrant cervical count further indicates that the Hox code may be conserved across living mammals. Our results are consistent with a mouse-like Hox code in the cervical vertebral column of sloths, with an anterior shift of HoxC-6 expression in association with the first thoracic vertebra in short-necked sloths, and a posterior shift of HoxC-5 and HoxC-6 expression in long-necked sloths. In combination with the presence of vertebral anomalies, these observations provide insights into the homeotic processes during development that involve morphological transformation of vertebrae as a result of changes in the Hox gene expression pattern. Nevertheless, the occurrence of PAR and thus related shifts of abaxial elements cannot be rejected by our findings. As both hypotheses may not be mutually exclusive, it is possible that parallel processes shape the overall anatomy of sloths necks . Moreover, processes resulting in the variation of cervical count are not necessarily the same in both genera. In conclusion, since hypothesis 1 (number of modules is retained but their boundaries are displaced) was not rejected by our analysis but was instead favored by the morphological modularity found here, both explanations remain plausible and may both be involved in the mammalian constraint of cervical count: indirect selection due to pleiotropy  and a developmental constraint associated with the muscular diaphragm in mammals .
Future analyses on the Hox code in non-model organisms, such as sloths, may yield direct evidence for the evolutionary mechanism responsible for the morphological adaptability of the axial skeleton. However, to date, the realization of these analyses is extremely limited. The present study provides a basis for further research that should include extinct taxa in order to trace the pattern and the underlying genetic mechanisms in the evolution of the vertebral column. Ultimately, this will further our understanding of the processes responsible for the 200-million-year old evolutionary constraint and the conserved three-subunit pattern that shapes mammalian cervical evolution .
The present study includes the complete cervical vertebral column of four sloths with variable number of vertebrae in the neck comprising three different species (Table 1).
Quantitative morphological analysis
The morphological variability within the cervical vertebral column is evaluated by geometric morphometrics. A linear regression method for landmark-based geometric morphometrics of vertebrae has been described by Head & Polly (2015) , but requires a minimum of at least 10–20 observations for regression analysis (cf. ). Therefore, we here follow the procedure applied by Böhmer et al. (2015a)  which allows the statistical assessment of shape changes between successive vertebrae in vertebral series comprising less than 10 vertebrae.
Our approach allows the statistical assessment of shape changes between successive vertebrae. A series of 15 homologous landmarks are digitized on the three-dimensional (3D) scans of the CV (C2 to C7) using the software LANDMARK v. 3.0  (Additional file 1: Figure S3). The homologous points capture the vertebral shape in 3D characterizing the morphology of the vertebral centrum and the neural arch. The atlas (first cervical vertebra) is not included in the analysis due to its unique morphology. It lacks specific serial homologies with postatlantal cervicals, and, thus, several landmarks cannot be applied to it.
Analysis and visualization of the geometric morphometric data is performed using the software MORPHOLOGIKA . Two data sets were analyzed: (1) the interspecific data set includes all CV of the four sloths together and (2) the intraneck data sets include all CV of each taxon separately. The interspecific data set allows evaluation of the morphological similarities of the CV across species. The intraneck data sets serve as a basis to identify the morphological modules in each vertebral series. The following procedure was performed on both types of data sets. First, the 3D coordinates of all landmarks were superimposed using a generalized Procrustes superimposition. It removes all the information unrelated to shape . Next, a relative warps analysis was performed to reduce the dimensionality of the dataset and to reveal the similarity relationships among the vertebrae within the cervical vertebral column. The relative warps analysis constructs a morphospace in which shape variation can be quantified. A cluster analysis using the single linkage algorithm in combination with the Euclidian similarity index was performed on the superimposed landmark coordinates. This joins the CV based on minimal distance between them and results in the quantitative establishment of the morphological subunit pattern in the cervical vertebral column.
Hox gene expression and morphological proxies
The somitic Hox gene expression pattern in the cervical vertebral column of the mouse was established by a literature survey in Böhmer (2017) . The expression of Hox genes of the paralogue groups (PG) 3 to 6 are involved in mediating the development of the cervical vertebral column (e.g., ). In particular, the anterior expression limits of Hox4 and Hox5 PG are responsible for the regional patterning in the neck and are the focus of the present study. The survey focused on embryonic stages at which the somites are developed along the full anteroposterior body axis and the somitic Hox gene expression limits are thought to be well established and stable during further development [16, 19, 23, 58]. Based on the demonstrated correlation between genomic control and phenotypic changes in crocodilians and birds (cf. ), the present study of morphological variation of the CV served as a Hox gene expression pattern proxy.
Since homeotic transformations induced by mutations of Hox genes may be incomplete (e.g., [52, 59, 71, 72] and may result in transitional vertebral identities, the vertebrae were analyzed for the presence of congenital anomalies (such as fusion of vertebrae, left/right asymmetry or rudimentary ribs), following previous studies [15, 26, 73].
Owen R. The principle forms of the skeleton and the teeth. London: Houlston & Stoneman; 1855.
Galis F. Why do almost all mammals have seven cervical vertebrae? Developmental constraints, Hox genes, and cancer. J Exp Zool B Mol Dev Evol. 1999;285(1):19–26.
Narita Y, Kuratani S. Evolution of the vertebral formulae in mammals: a perspective on developmental constraints. J Exp Zool B Mol Dev Evol. 2005;304:91–106.
Gadow HF. The evolution of the vertebral column. A contribution to the study of vertebrate phylogeny. London: Cambridge University Press; 1933.
Slijper EJ. Comparative biologic-anatomical investigation on the vertebral column and spinal musculature of mammals. Verh Kon Ned Ak Wet Natuurk (Tweede Sectie). 1946;42(5):1–128.
Buchholtz EA, Bailin HG, Laves SA, Yang JT, Chan MY, Drozd LE. Fixed cervical count and the origin of the mammalian diaphragm. Evol Dev. 2012;14(5):399–411.
Buchholtz EA. Crossing the frontier: a hypothesis for the origins of meristic constraint in mammalian axial patterning. Zoology (Jena). 2014;117(1):64–9.
Galis F, Metz JA. Evolutionary novelties: the making and breaking of pleiotropic constraints. Integr Comp Biol. 2007;47(3):409–19.
McGuigan K, Rowe L, Blows MW. Pleiotropy, apparent stabilizing selection and uncovering fitness optima. Trends Ecol Evol. 2011;26(1):22–9.
Wagner GP, Zhang J. The pleiotropic structure of the genotype-phenotype map: the evolvability of complex organisms. Nat Rev Genet. 2011;12(3):204–13.
Guillaume F, Otto SP. Gene functional trade-offs and the evolution of pleiotropy. Genetics. 2012;192(4):1389–409.
Paaby AB, Rockman MV. The many faces of pleiotropy. Trends Genet. 2013;29(2):66–73.
Grüneberg H. The pathology of Development A study of inherited skeletal disorders in Animals. Oxford: Blackwell Scientific; 1963.
Galis F, Van Dooren TJ, Feuth JD, Metz JA, Witkam A, Ruinard S, Steigenga MJ, Wijnaendts LC. Extreme selection in humans against homeotic transformations of cervical vertebrae. Evolution. 2006;60(12):2643–54.
Varela-Lasheras I, Bakker AJ, van der Mije SD, Metz JA, van Alphen J, Galis F. Breaking evolutionary and pleiotropic constraints in mammals: on sloths, manatees and homeotic mutations. EvoDevo. 2011;2:11.
Böhmer C, Rauhut OWM, Wörheide G. Correlation between Hox code and vertebral morphology in archosaurs. Proc Biol Sci B. 2015;282:20150077.
Böhmer C. Correlation between Hox code and vertebral morphology in the mouse: towards a universal model for Synapsida. Zoological Letters. 2017;3(8):1–11.
Kessel M, Gruss P. Murine developmental control genes. Science. 1990;249:374–9.
Burke AC, Nelson CE, Morgan BA, Tabin C. Hox genes and the evolution of vertebrate axial morphology. Development. 1995;121(2):333–46.
Arnold P, Forterre F, Lang J, Fischer MS. Morphological disparity, conservatism, and integration in the canine lower cervical spine: insights into mammalian neck function and regionalization. Mamm Biol. 2016;81(2):153–62.
Arnold P, Amson E, Fischer MS. Differential scaling patterns of vertebrae and the evolution of neck length in mammals. Evolution. 2017;71(6):1587–99.
Johnson DR, McAndrew TJ, Oguz Ö. Shape differences in the cervical and upper thoracic vertebrae in rats (Rattus norvegicus) and bats (Pteropus poiocephalus): can we see shape patterns derived from position in column and species membership? J Anat. 1999;194(Pt 2):249–53.
Böhmer C, Rauhut OWM, Wörheide G. New insights into the vertebral Hox code of archosaurs. Evol Dev. 2015;17(5):258–69.
Flower WH. An Introduction to the Osteology of the Mammalia. London: Macmillan and Co.; 1885.
Giffin EB, Gillett M. Neurological and osteological definitions of cervical vertebrae in mammals. Brain Behav Evol. 1996;47:214–8.
Buchholtz EA, Stepien CC. Anatomical transformation in mammals: developmental origin of aberrant cervical anatomy in tree sloths. Evol Dev. 2009;11(1):69–79.
Hautier L, Weisbecker V, Sanchez-Villagra MR, Goswami A, Asher RJ. Skeletal development in sloths and the evolution of mammalian vertebral patterning. Proc Natl Acad Sci U S A. 2010;107(44):18903–8.
Nyakatura JA. The convergent evolution of suspensory posture and locomotion in tree sloths. J Mamm Evol. 2012;19(3):225–34.
Vaughan TA, Ryan JM, Czaplewski NJ. Mammalogy. 6th ed. Jones & Bartlett Learning: Massachusetts; 2015.
Bateson W. Materials for the study of variation treated with especial regard to discontinuity in the origin of species. London: Macmillan and Co; 1894.
Buckland W. IV. On the adaptation of the structure of the sloths to their peculiar mode of life. Trans Linn Soc Lond. 1834;17(1):17–27.
Miller RA. Functional adaptations in the forelimb of the sloths. J Mammal. 1935;16(1):38–51.
Galis F, Metz JA. Anti-cancer selection as a source of developmental and evolutionary constraints. Bioessays. 2003;25(11):1035–9.
Buchholtz EA, Wayrynen KL, Lin IW. Breaking constraint: axial patterning in Trichechus (Mammalia: Sirenia). Evol Dev. 2014;16(6):382–93.
Randau M, Goswami A. Morphological modularity in the vertebral column of Felidae (Mammalia, Carnivora). BMC Evol Biol. 2017;17(1):133.
Zajac FE. Muscle coordination of movement: a perspective. J Biomech. 1993;26(Suppl 1):109–24.
Krings M, Nyakatura JA, Boumans M, Fischer MS, Wagner H. Barn owls maximize head rotations by a combination of yawing and rolling in functionally diverse regions of the neck. J Anat. 2017;231(1):12–22.
Bernstein N. On the construction of movements. Moscow: Medgiz; 1947.
Graf W, de Waele C, Vidal PP. Functional anatomy of the head-neck movement system of quadrupedal and bipedal mammals. J Anat. 1995;186:55–74.
Vidal PP, Graf W, Berthoz A. The orientation of the cervical vertebral column in unrestrained awake animals. I Resting position. Exp Brain Res. 1986;61(3):549–59.
De Waele C, Graf W, Josset P, Vidal PP. A radiological analysis of the postural syndromes following hemilabyrinthectomy and selective canal and otolith lesions in the Guinea pig. Exp Brain Res. 1989;77(1):166–82.
Krings M, Nyakatura JA, Fischer MS, Wagner H. The cervical spine of the American barn owl (Tyto furcata pratincola): I. Anatomy of the vertebrae and regionalization in their S-shaped arrangement. PLoS One. 2014;9(3):e91653.
Zweers G, Bout R, Heidweiller J. Motor organization of the avian head-neck system. In: MNO D, Green PR, editors. Perception and motor control in birds. Berlin: Springer; 1994. p. 201–21.
Bout RG. Postures on the avian Craniocervical column. J Morphol. 1997;231:287–95.
Gunji M, Endo H. Functional cervicothoracic boundary modified by anatomical shifts in the neck of giraffes. R Soc Open Sci. 2016;3(2):150604.
Nyakatura JA, Stark H. Aberrant back muscle function correlates with intramuscular architecture of dorsovertebral muscles in two-toed sloths. Mamm Biol. 2015;80(2):114–21.
Arnold P, Esteve-Altava B, Fischer MS. Musculoskeletal networks reveal topological disparity in mammalian neck evolution. BMC Evol Biol. 2017;17(1):251.
Nyakatura JA, Fischer MS. Functional morphology of the muscular sling at the pectoral girdle in tree sloths: convergent morphological solutions to new functional demands? J Anat. 2011;219(3):360–74.
Reighard J, Jennings HS. Anatomy of the cat. New York: Henry Holt and Company; 1902.
Windle BCA, Parsons FG. On the myology of the Edentata. Proc Zool Soc Lond. 1899;1899:990–1017.
Ohya YK, Kuraku S, Kuratani S. Hox code in embryos of Chinese soft-shelled turtle Pelodiscus sinensis correlates with the evolutionary innovation in the turtle. J Exp Zool B Mol Dev Evol. 2005;304:107–18.
McIntyre DC, Rakshit S, Yallowitz AR, Loken L, Jeannotte L, Capecchi MR, Wellik DM. Hox patterning of the vertebrate rib cage. Development. 2007;134(16):2981–9.
Moraes-Barros N, Chiarello A, Plese T. 2014. Bradypus variegatus. The IUCN Red List of Threatened Species. 2014:e.T3038A47437046.http://0-dx.doi.org.brum.beds.ac.uk/10.2305/IUCN.UK.20141.RLTS.T3038A47437046.en.
Chiarello A, Moraes-Barros N. 2014. Bradypus tridactylus. The IUCN Red List of Threatened Species. 2014:e.T3037A47436865. http://0-dx.doi.org.brum.beds.ac.uk/10.2305/IUCN.UK.20141.RLTS.T3037A47436865.en.
Villavicencio-Lorini P, Kuss P, Friedrich J, Haupt J, Farooq M, Turkmen S, Duboule D, Hecht J, Mundlos S. Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. J Clin Invest. 2010;120(6):1994–2004.
Aoyama H, Mizutani-Koseki S, Koseki H. Three developmental compartments involved in rib formation. Int J Dev Biol. 2005;49(2–3):325–33.
Burke AC, Nowicki JL. A new view of patterning domains in the vertebrate mesoderm. Dev Cell. 2003;4(2):159–65.
Mansfield JH, Abzhanov A. Hox expression in the American alligator and evolution of archosaurian axial patterning. J Exp Zool B Mol Dev Evol. 2010;314:1–16.
Jeannotte L, Lemieux M, Charron J, Poirier F, Robertson EJ. Specification of axial identity in the mouse: role of the Hoxa-5 (Hox1.3) gene. Genes Dev. 1993;7(11):2085–96.
Aubin J, Lemieux M, Tremblay M, Behringer RR, Jeannotte L. Transcriptional interferences at the Hoxa4/Hoxa5 locus: importance of correct Hoxa5 expression for the proper specification of the axial skeleton. Dev Dyn. 1998;212(1):141–56.
Chen JW, Zahid S, Shilts MH, Weaver SJ, Leskowitz RM, Habbsa S, Aronowitz D, Rokins KP, Chang Y, Pinnella Z, et al. Hoxa-5 acts in segmented somites to regulate cervical vertebral morphology. Mech Dev. 2013;130(4–5):226–40.
Crompton AW, Jenkins FA Jr. Mammals from reptiles: a review of mammalian origins. Annu Rev Earth Planet Sci. 1973;1:131–55.
Rose KD. The beginning of the age of mammals. Baltimore: The Johns Hopkins University Press; 2006.
Müller J, Scheyer TM, Head JJ, Barrett PM, Werneburg I, Ericson PGP, Pol D, Sánchez-Villagra MR. Homeotic effects, somitogenesis and the evolution of vertebral numbers in recent and fossil amniotes. Proc Natl Acad Sci U S A. 2010;107(5):2118–23.
Head JJ, Polly PD. Evolution of the snake body form reveals homoplasy in amniote Hox gene function. Nature. 2015;520:86–9.
Harrell FE Jr. Regression modeling strategies. With applications to linear models, logistic regression, and survival analysis. New York: Springer; 2001.
Wiley DF. Landmark. In: 3.0 EDN. University of California, Davis: Institute for Data Analysis and Visualization (IDAV); 2005.
O'Higgins P, Jones N. Morphologika2. 2.5 ed: Hull York Medical School; 2006. http://hyms.fme.googlepages.com/downloadmorphologica.
Rohlf FJ, Slice D. Extensions of the Procrustes method for optimal superimposition of landmarks. Syst Zool. 1990;39(1):40–59.
Mallo M, Wellik DM, Deschamps J. Hox genes and regional patterning of vertebrate body plan. Dev Biol. 2010;344:7–15.
Horan GSB, Kovàcs EN, Behringer RR, Featherstone MS. Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton: evidence for unique and redundant function. Dev Biol. 1995;169:359–72.
Rancourt DE, Tsuzuki T, Capecchi MR. Genetic interaction between hoxb-5 and hoxb-6 is revealed by nonallelic noncomplementation. Genes Dev. 1995;9(1):108–22.
Endo H, Hashimoto O, Taru H, Sugimura K, Fujiwara S-i, Itou T, Koie H, Kitagawa M, Sakai T. Comparative morphological examinations of the cervical and thoracic vertebrae and related spinal nerves in the two-toed sloth. Mammal Study. 2013;38(3):217–24.
Availability of data and material
All data generated or analyzed during this study are included in this published article [and its additional file].
PA was funded by the Max Planck Society. EA was funded by the Alexander von Humboldt Foundation. JAN and EA were funded by the Deutsche Forschungsgemeinschaft (DFG EXC 1027 and DFG AM 517/1–1).
Ethics approval and consent to participate
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S1. Results of cluster analysis for each specimen. A three subunit pattern was revealed in all specimens analyzed. Green, axis; yellow, anterior subunit; red, posterior subunit. A, C. cf. didactylus 1; B, C. didactylus 2; C, B. variegatus; D, B. tridactylus. Figure S2. 3D renderings of all analyzed vertebrae. For each specimen left lateral view above and anterior view below. A, C. cf. didactylus 1; B, C. didactylus 2; C, B. variegatus; D, B. tridactylus. C1 (atlas) of B. tridactylus was not available with the museum specimen. Note that the present analysis involved only postatlantal CV. Figure S3. Landmark set used in the 3D geometric morphometric analysis. The numbered 3D landmarks (red points) are shown on a mid-cervical vertebra of Bradypus tridactylus (3D model). LM1 = dorsal-anterior edge of vertebral centrum, LM2 = ventral-anterior edge of vertebral centrum, LM3 = ventral-posterior edge of vertebral centrum, LM4 = dorsal-posterior edge of vertebral centrum, LM5 = anteriormost edge of articular facet of postzygapophysis, LM6 = dorsal-posterior edge of articular facet of postzygapophysis, LM7 = point of maximum curvature between postzygapophysis and neural spine, LM8 = posterior edge of neural spine, LM9 = anterior edge of neural spine, LM10 = point of maximum curvature between neural spine and prezygapophysis, LM11 = posteriormost point of articular facet of prezygapophysis, LM12 = dorsal-anterior edge of articular facet of prezygapophysis, LM13 = dorsalmost point of vertebral centrum in anterior view, LM14 = lateralmost point of vertebral centrum in anterior view, LM15 = ventralmost point of vertebral centrum in anterior view. Table S1. Percentage of total variance explained and cumulative variance per relative warp (RW). Only the first four RWs are indicated since they explain more than 95% of the total variance. (DOCX 578 kb)
About this article
Cite this article
Böhmer, C., Amson, E., Arnold, P. et al. Homeotic transformations reflect departure from the mammalian ‘rule of seven’ cervical vertebrae in sloths: inferences on the Hox code and morphological modularity of the mammalian neck. BMC Evol Biol 18, 84 (2018) doi:10.1186/s12862-018-1202-5
- Axial patterning
- Hox genes
- Cervical vertebrae