A catalogue of Bilaterian-specific genes – their function and expression profiles in early development

Author:

Krämer-Eis Andrea,Ferretti Luca,Schiffer Philipp H.,Heger Peter,Wiehe ThomasORCID

Abstract

AbstractBilateria constitute a monophyletic group of organisms comprising about 99% of all living animals. Since their initial radiation about 540Mya they have evolved a plethora of traits and body forms allowing them to conquer almost any habitat on earth. There are only few truly uniting and shared morphological features retained across the phylum. Unsurprisingly, also the genetic toolkit of bilateria is highly diverged.In the light of this divergence we investigated if a set of bilaterian-specific genes exists and, beyond this, if such genes are related with respect to function and expression patterns among organisms as distant as Drosophila, Caenorhabditis and Danio. Using a conservative pyramidal approach of orthology inference we collected a set of protein-coding genes which have orthologs in all major branches of Bilateria, but no homologs in non-bilaterian species. To characterize the proteins with respect to function, we employ a novel method for multi-species GO analysis and augmented it by a human-curated annotation based on an extensive literature search. Finally, we extracted characteristic developmental expression profiles for Bilateria from the extensive data available for three model organisms and we explored the relation between expression and function.Among an initial set of several hundred candidates we identified 85 clusters of orthologous proteins which passed our filter criteria for bilaterian specificity. Although some of these proteins belong to common developmental processes, they cover a wide range of biological components, from transcription factors to metabolic enzymes. For instance, the clusters include myoD, an important regulator of mesodermal cell fate and muscle development, and prospero and several other factors involved in nervous system development. Our results reveal a so far unknown connection between morphological key innovations of bilateria, such as the mesoderm and a complex nervous system, and their genetic basis. Furthermore, we find typical expression profiles for these bilaterian specific genes, with the majority of them being highly expressed when the adult body plan is constructed. These observations are compatible with the idea that bilaterians are characterized by the unfolding of a new developmental phase, namely the transition of the larva to morphologically distinct adults.Author SummaryBilateria represent by far the largest and morphologically most diverse clade of all extant animals. The bilaterian radiation dates back to the so-called Cambrian explosion of species. Although bilateria show a large variety of very distinct body plans, they are also characterized by several common developmental and morphological traits, on which their monophyly is based. Here, we wanted to know whether these common phenotypic features may also have a shared and conserved genetic basis. To address this question we compared the proteomes of bilaterian and non-bilaterian species and extracted an initial set of a few hundred candidate proteins. Their underlying genes were further post-processed by means of orthology clustering, multi-species GO enrichment, expression analysis and extensive literature mining. This resulted in a thorough set of genes with roles in body morphology-, neuronal system‐ and muscle development, as well as in cell-cell signalling processes. This gene catalogue can be regarded as blue-print of a common bilaterian pheno‐ or morphotype and should contain highly interesting targets for further functional studies in model and non-model organisms.

Publisher

Cold Spring Harbor Laboratory

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cambrian explosion;Epigenetic Mechanisms of the Cambrian Explosion;2020

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3