- Research article
- Open Access
Diminution of pharyngeal segmentation and the evolution of the amniotes
© The Author(s). 2019
- Received: 23 November 2018
- Accepted: 5 February 2019
- Published: 11 February 2019
The pharyngeal arches are a series of bulges found on the lateral surface of the head of vertebrate embryos, and it is within these segments that components of the later anatomy are laid down. In most vertebrates, the post-otic pharyngeal arches will form the branchial apparatus, while in amniotes these segments are believed to generate the larynx. It has been unclear how the development of these segments has been altered with the emergence of the amniotes.
In this study, we examined the development of pharyngeal arches in amniotes and show that the post-otic pharyngeal arches in this clade are greatly diminished. We find that the post-otic segments do not undergo myogenesis or skeletogenesis, but are remodelled before these processes occur. We also find that nested DLX expression, which is a feature of all the pharyngeal arches in anamniotes, is associated with the anterior segments but less so with the posterior arches in amniotes. We further show that the posterior arches of the mouse embryo fail to properly delineate, which demonstrates the lack of function of these posterior segments in later development.
In amniotes, there has been a loss of the ancestral “branchial” developmental programme that is a general feature of gnathostomes; myogenesis and skeletogenesis This is likely to have facilitated the emergence of the larynx as a new structure not constrained by the segmental organisation of the posterior pharyngeal region.
- Pharyngeal segmentation
- Pharyngeal pouch
- Pharyngeal arch
- Amniote evolution
The development of the pharyngeal arches is underpinned by the generation of the pharyngeal pouches, outpocketings of the endoderm, which contact the overlying ectoderm, with the other constituents of the arches, the neural crest and mesoderm, migrating into these preformed segmental units . These embryonic populations differentiate to form a range of derivatives: the neural crest gives rise to the skeletal and connective tissues, the mesoderm to the musculature and the blood vessels, the ectoderm to the epidermis and sensory neurons and the endoderm the lining of the pharynx and a range of specialised organs. Thus, the arches constitute an iterated series with each forming the same components. In many vertebrate clades, this embryonic segmental organisation is translated into the later functional anatomy and is evident in the serial arrangement of the gill-bearing branchial arches.
In post-metamorphic amphibia and in amniotes, however, the branchial skeleton is lost and the larynx develops [2, 3]. This structure is a feature of tetrapods that connects the pharynx with the trachea and plays an essential role in facilitating life on land. The larynx consists of skeletal elements, which include the cricoid and paired arytenoids in most tetrapods as well as, in mammals, the thyroid, and associated muscular and connective tissue elements . Developmentally, the components of the larynx are thought to have their origins in the posterior, post-otic, pharyngeal arches and thus to be equivalent to the derivatives of the posterior arches in other vertebrates, the branchial apparatus [2, 4]. Indeed, it is generally assumed that there is a correspondence between the mature structures of the larynx: skeleton, muscle and nerves, and the embryonic pharyngeal segments, and such a relationship is a staple of embryology and anatomy textbooks [4–9].
In this study, we assessed the early development of the posterior pharyngeal arches and their subsequent envelopment by the second arch. We further document the relationship between the pharyngeal segments and the formation of the muscular and skeletal derivatives. We find that while there is a clear correspondence between these events and the anterior arches, this is not the case for the posterior segments. Thus, while the processes of myogenesis and chondrogenesis are underway at several sites in the embryo, they are not a feature of the posterior pharyngeal region. We further show that, although the anterior pharyngeal segments exhibit nested DLX gene expression, the expression of these genes is greatly reduced in the posterior arches, suggesting that the need to regionalise the neural crest along the proximodistal axis in these segments is less in amniotes. We note that the reduction in DLX expression is more extensive in the mouse than in the chick, and this prompted us to further investigate differences between the posterior segments in these species. Interestingly, we find that while the 4th pharyngeal pouch contacts the ectoderm in chick and human embryos, it does not do so in mice. Consequently, the posterior pharyngeal segments are not fully delineated in this species, which further underscores their lack of significance for later events.
We further analysed muscle and cartilage differentiation at later stages while the second arch is covering the posterior arches. In chick at HH25, MYOD staining can be seen in the first and second arch, but not in the more posterior pharynx (Fig. 3c, d), even though these segments have a resident mesodermal population (Fig. 2). However, it is also clear that myogenesis is well underway in other areas of the embryo including the myotome of the somites and myoblasts migrating into the limbs. Similarly, in the mouse at TS17, myogenesis is evident in the first two arches, in the myotome and in the myoblasts populating the forelimb. Yet, there is no myogenesis within the posterior arches at this stage, bar the migratory hypoglossal myoblasts (Fig. 3e). We also used COL2A staining to reveal sites of chondrogenesis at these later stages. We find that, while there is extensive chondrogenesis in the somites and the limbs, in the chick at HH25, there is little chondrogenesis in the pharynx. COL2A staining is evident in the first and second arches, but not in the more posterior arches (Fig. 3g). In the mouse at TS17, we also found chondrogenesis underway in the somites and limbs, and while there was some staining in the first two arches, the posterior was devoid of COL2A expression (Fig. 3h). Thus, we find that the posterior pharyngeal segments do not entertain myogenesis or skeletogenesis during their period of definition.
These differences in DLX expression in the posterior arches between chick and mouse prompted us to further analyse the underlying organisation of the arches. Central to the organisation of the pharyngeal arches is the establishment of the contact between the pharyngeal pouches and the overlying ectoderm. This serves to define the anterior and posterior limits of the arches and to segregate the mesenchymal populations of the different arches. We have previously documented the formation of the pharyngeal pouches and arches in detail in chick  and we therefore assessed if the topology of the mouse pouches and arches were the same. Notably, we find that in mouse the fourth pouch does not contact the ectoderm and thus neither establishes a clearly delineated posterior boundary of the fourth arch nor an anterior boundary of the sixth arch (Fig. 5a). We further analysed HREM (high-resolution episcopic microscopy) data of 25 E10.5 mouse embryos (TS16/17) catalogued on the DMDD website (https://dmdd.org.uk/), to determine if the failure of the fourth pouch to contact the ectoderm represented a temporal effect. However, we found that in every embryo analysed, the fourth pouch does not contact the ectoderm and this was observed in embryos that varied between 3.7 mm to 5.2 mm crown rump length, and that were either in the segmental or early post-segmental phases of development. We further analysed human embryo resources to determine if this is a general feature of mammals or a derived feature of mice. We examined HREM data from the four Carnegie stage (CS)15 human embryos catalogued on the DMDD website; this is the stage in humans at which all the arches have formed. In each we noted that the fourth pouch could be seen to contact the ectoderm (Fig. 5b). This same topology was also found in histological sections of a CS15 embryo archived on the Virtual Human embryo database (https://www.prenatalorigins.org/virtual-human-embryo/stage.php?stage=15). Thus, the mouse represents a test of whether the failure to fully establish the posterior pharyngeal segments has any impact on later anatomy; clearly, it does not, and the larynx forms.
A key observation from this study is that the development of the posterior pharyngeal arches in amniotes is markedly different from that of other vertebrate clades. In anamniotes, the posterior arches generate muscular and skeletal structures, exhibit nested expression of DLX linked pairs and these segments form the blueprint for the organisation of the branchial apparatus [12, 15–18, 22]. We show here that in chick and mouse the posterior arches do not undergo myogenesis or skeletogenesis while they exist as morphologically discernible entities, and that they exhibit reduced nested expression of the DLX genes; there has been a suppression of the inner fish here. Consequently, the segmental organisation of the posterior embryonic pharynx has little significance for the later musculoskeletal anatomy; a point underscored by the fact that, in mouse, the posterior arches fail to fully emerge. Thus, these results lay bare the fact that the correspondence between the pharyngeal arches and the components of the larynx, invariably found in anatomy and embryology textbooks, is but supposition [4, 6–9].
Finally, it should also be noted that while the skeletal components of the branchial apparatus of anamniotes are generally neural crest derived [23, 24], this is not the case for the larynx. Fate mapping studies in birds have demonstrated that the laryngeal cartilages, the cricoid and arytenoid, arise from the lateral plate mesoderm . Similarly, a recent study in mouse has also shown a mesodermal origin for the cricoid and arytenoid cartilages . However, the thyroid cartilage, which is a mammalian novelty, seems to have a more complex origin comprising both a crest derived and a mesodermal component . Thus, the evolution of the larynx cannot have involved a transformation of the developmental programme that would have directed the generation of the branchial apparatus, but rather the larynx emerges as a new structure.
Chick embryos were staged according to Hamburger and Hamilton  and mice according to Theiler . The following mouse lines were used: Wnt1-cre driver: Tg (Wnt1-cre)11Rth  and reporter line: R26RmT/mG: GT (Rosa)26Sortm4(ACTB-tdTomato-EGFP) . All animal work was performed in accordance with UK Home Office Regulations. The HREM data from the human embryos is from the DMDD website (https://dmdd.org.uk/). Data from Deciphering the Mechanisms of Developmental Disorders (https://dmdd.org.uk/), a programme funded by the Wellcome Trust with support from the Francis Crick Institute, is licensed under a Creative Commons Attribution licence.
In situ hybridisation
Embryos were fixed in in 3.7% (v/v) formaldehyde in PBS and in situ hybridisation carried out as previously described . Gene expression was either examined as whole mounts or embryos were embedded in 20% (w/v) gelatin in PBS and sectioned using a vibratome.
CCSFE labelling was carried out as previously described .
We would like to thank Dr. Tom Mohun, Crick Institute London, for help with the HREM analysis of the Human and mouse embryos. We thank Caroline Formstone, Clemens Kiecker, Malcolm Logan and Jill Sales for comments on the text.
This work was funded by a BBSRC grant (BB/R006199/1) to AG.
Availability of data and materials
All data and material are available from the corresponding author. email@example.com.
The project was conceived by AG. The experimental work was carried out by SP, JR, AS, AD, KL and AG. The paper was written by AG and SP with JR, AS, AD and KL commenting and modifying the draft. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All embryo collection was carried out as prescribed by the UK Animals (Scientific Procedures) Act 1986.
Consent for publication
All authors consent to publication.
The authors declare that they have no competing interests.
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