Investigating the association between germ line specification and sequence evolution in vertebrates

Within vertebrates the primordial germ cells (PGCs) can either be induced by embryonic signals (known as epigenesis), or predetermined by maternally deposited germ plasm (preformation). Epigenesis is known to be the ancestral mechanism, while preformation has evolved multiple times. Epigenesis has b...

Full description

Bibliographic Details
Main Author: Evans, Teri
Format: Thesis (University of Nottingham only)
Language:English
English
Published: 2015
Online Access:https://eprints.nottingham.ac.uk/28505/
_version_ 1848793585298702336
author Evans, Teri
author_facet Evans, Teri
author_sort Evans, Teri
building Nottingham Research Data Repository
collection Online Access
description Within vertebrates the primordial germ cells (PGCs) can either be induced by embryonic signals (known as epigenesis), or predetermined by maternally deposited germ plasm (preformation). Epigenesis is known to be the ancestral mechanism, while preformation has evolved multiple times. Epigenesis has been proposed to enforce a developmental constraint on the evolution of somatic structures that is released in species which acquired preformation. In accordance with this hypothesis, the mesoderm gene regulatory network is conserved between urodeles and mammals, which have retained epigenesis, but has diverged in anurans (preformation). An increase in speciation has also been shown in vertebrates which have acquired preformation. Our aims were to investigate whether the mode of PGC specification associates with the molecular evolution of protein-coding genes. We downloaded all publicly available vertebrate sequences. These were combined with our three novel transcriptomes from axolotl, sturgeon and lungfish. In line with previous analyses, we built 4-taxon trees to investigate the extent of phylogenetic incongruence. This revealed a bias associated with the mode of PGC specification, caused by a significant difference in the rate of evolution. Many genes in species that have acquired preformation are evolving significantly faster than in their sister taxa undergoing epigenesis. These sequences are typically expressed in early development, and are ancient genes with known orthologs at the base of Eukaryotes. Additionally, we show that Oct4 and Nanog, which are crucial for pluripotency, have been lost in taxa using preformation. Therefore our results are consistent with the proposal that developmental constraint, imposed by epigenesis, is released in species undergoing preformation.
first_indexed 2025-11-14T19:02:38Z
format Thesis (University of Nottingham only)
id nottingham-28505
institution University of Nottingham Malaysia Campus
institution_category Local University
language English
English
last_indexed 2025-11-14T19:02:38Z
publishDate 2015
recordtype eprints
repository_type Digital Repository
spelling nottingham-285052025-02-28T11:33:50Z https://eprints.nottingham.ac.uk/28505/ Investigating the association between germ line specification and sequence evolution in vertebrates Evans, Teri Within vertebrates the primordial germ cells (PGCs) can either be induced by embryonic signals (known as epigenesis), or predetermined by maternally deposited germ plasm (preformation). Epigenesis is known to be the ancestral mechanism, while preformation has evolved multiple times. Epigenesis has been proposed to enforce a developmental constraint on the evolution of somatic structures that is released in species which acquired preformation. In accordance with this hypothesis, the mesoderm gene regulatory network is conserved between urodeles and mammals, which have retained epigenesis, but has diverged in anurans (preformation). An increase in speciation has also been shown in vertebrates which have acquired preformation. Our aims were to investigate whether the mode of PGC specification associates with the molecular evolution of protein-coding genes. We downloaded all publicly available vertebrate sequences. These were combined with our three novel transcriptomes from axolotl, sturgeon and lungfish. In line with previous analyses, we built 4-taxon trees to investigate the extent of phylogenetic incongruence. This revealed a bias associated with the mode of PGC specification, caused by a significant difference in the rate of evolution. Many genes in species that have acquired preformation are evolving significantly faster than in their sister taxa undergoing epigenesis. These sequences are typically expressed in early development, and are ancient genes with known orthologs at the base of Eukaryotes. Additionally, we show that Oct4 and Nanog, which are crucial for pluripotency, have been lost in taxa using preformation. Therefore our results are consistent with the proposal that developmental constraint, imposed by epigenesis, is released in species undergoing preformation. 2015-07-15 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/28505/1/Thesis.pdf application/pdf en arr https://eprints.nottingham.ac.uk/28505/7/Thesis-evans-offpages.pdf Evans, Teri (2015) Investigating the association between germ line specification and sequence evolution in vertebrates. PhD thesis, University of Nottingham.
spellingShingle Evans, Teri
Investigating the association between germ line specification and sequence evolution in vertebrates
title Investigating the association between germ line specification and sequence evolution in vertebrates
title_full Investigating the association between germ line specification and sequence evolution in vertebrates
title_fullStr Investigating the association between germ line specification and sequence evolution in vertebrates
title_full_unstemmed Investigating the association between germ line specification and sequence evolution in vertebrates
title_short Investigating the association between germ line specification and sequence evolution in vertebrates
title_sort investigating the association between germ line specification and sequence evolution in vertebrates
url https://eprints.nottingham.ac.uk/28505/