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Lizards possess the most complete tetrapod Hox gene repertoire despite pervasive structural changes in Hox clusters

Feiner, Nathalie LU and Wood, Natalie J. (2019) In Evolution and Development 21(4). p.218-228
Abstract

Hox genes are a remarkable example of conservation in animal development and their nested expression along the head-to-tail axis orchestrates embryonic patterning. Early in vertebrate history, two duplications led to the emergence of four Hox clusters (A-D) and redundancy within paralog groups has been partially accommodated with gene losses. Here we conduct an inventory of squamate Hox genes using the genomes of 10 lizard and 7 snake species. Although the HoxC1 gene has been hypothesized to be lost in the amniote ancestor, we reveal that it is retained in lizards. In contrast, all snakes lack functional HoxC1 and -D12 genes. Varying levels of degradation suggest differences in the process of gene loss between the two genes. The... (More)

Hox genes are a remarkable example of conservation in animal development and their nested expression along the head-to-tail axis orchestrates embryonic patterning. Early in vertebrate history, two duplications led to the emergence of four Hox clusters (A-D) and redundancy within paralog groups has been partially accommodated with gene losses. Here we conduct an inventory of squamate Hox genes using the genomes of 10 lizard and 7 snake species. Although the HoxC1 gene has been hypothesized to be lost in the amniote ancestor, we reveal that it is retained in lizards. In contrast, all snakes lack functional HoxC1 and -D12 genes. Varying levels of degradation suggest differences in the process of gene loss between the two genes. The vertebrate HoxC1 gene is prone to gene loss and its functional domains are more variable than those of other Hox1 genes. We describe for the first time the HoxC1 expression patterns in tetrapods. HoxC1 is broadly expressed during development in the diencephalon, the neural tube, dorsal root ganglia, and limb buds in two lizard species. Our study emphasizes the value of revisiting Hox gene repertoires by densely sampling taxonomic groups and its feasibility owing to growing sequence resources in evaluating gene repertoires across taxa.

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author
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Evolution and Development
volume
21
issue
4
pages
11 pages
publisher
Wiley-Blackwell
external identifiers
  • pmid:31298799
  • scopus:85068968535
ISSN
1520-541X
DOI
10.1111/ede.12300
language
English
LU publication?
yes
id
74ce532d-7b85-44fa-87fc-793ce82c0259
date added to LUP
2019-07-23 13:13:59
date last changed
2024-06-25 23:54:22
@article{74ce532d-7b85-44fa-87fc-793ce82c0259,
  abstract     = {{<p>Hox genes are a remarkable example of conservation in animal development and their nested expression along the head-to-tail axis orchestrates embryonic patterning. Early in vertebrate history, two duplications led to the emergence of four Hox clusters (A-D) and redundancy within paralog groups has been partially accommodated with gene losses. Here we conduct an inventory of squamate Hox genes using the genomes of 10 lizard and 7 snake species. Although the HoxC1 gene has been hypothesized to be lost in the amniote ancestor, we reveal that it is retained in lizards. In contrast, all snakes lack functional HoxC1 and -D12 genes. Varying levels of degradation suggest differences in the process of gene loss between the two genes. The vertebrate HoxC1 gene is prone to gene loss and its functional domains are more variable than those of other Hox1 genes. We describe for the first time the HoxC1 expression patterns in tetrapods. HoxC1 is broadly expressed during development in the diencephalon, the neural tube, dorsal root ganglia, and limb buds in two lizard species. Our study emphasizes the value of revisiting Hox gene repertoires by densely sampling taxonomic groups and its feasibility owing to growing sequence resources in evaluating gene repertoires across taxa.</p>}},
  author       = {{Feiner, Nathalie and Wood, Natalie J.}},
  issn         = {{1520-541X}},
  language     = {{eng}},
  month        = {{07}},
  number       = {{4}},
  pages        = {{218--228}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{Evolution and Development}},
  title        = {{Lizards possess the most complete tetrapod Hox gene repertoire despite pervasive structural changes in Hox clusters}},
  url          = {{http://dx.doi.org/10.1111/ede.12300}},
  doi          = {{10.1111/ede.12300}},
  volume       = {{21}},
  year         = {{2019}},
}