Cargando…

A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals

BACKGROUND: Ducks have a typical avian karyotype that consists of macro- and microchromosomes, but a pair of much less differentiated ZW sex chromosomes compared to chickens. To elucidate the evolution of chromosome architectures between ducks and chickens, and between birds and mammals, we produced...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Jing, Zhang, Jilin, Liu, Jing, Zhou, Yang, Cai, Cheng, Xu, Luohao, Dai, Xuelei, Feng, Shaohong, Guo, Chunxue, Rao, Jinpeng, Wei, Kai, Jarvis, Erich D, Jiang, Yu, Zhou, Zhengkui, Zhang, Guojie, Zhou, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787181/
https://www.ncbi.nlm.nih.gov/pubmed/33406261
http://dx.doi.org/10.1093/gigascience/giaa142
_version_ 1783632775640776704
author Li, Jing
Zhang, Jilin
Liu, Jing
Zhou, Yang
Cai, Cheng
Xu, Luohao
Dai, Xuelei
Feng, Shaohong
Guo, Chunxue
Rao, Jinpeng
Wei, Kai
Jarvis, Erich D
Jiang, Yu
Zhou, Zhengkui
Zhang, Guojie
Zhou, Qi
author_facet Li, Jing
Zhang, Jilin
Liu, Jing
Zhou, Yang
Cai, Cheng
Xu, Luohao
Dai, Xuelei
Feng, Shaohong
Guo, Chunxue
Rao, Jinpeng
Wei, Kai
Jarvis, Erich D
Jiang, Yu
Zhou, Zhengkui
Zhang, Guojie
Zhou, Qi
author_sort Li, Jing
collection PubMed
description BACKGROUND: Ducks have a typical avian karyotype that consists of macro- and microchromosomes, but a pair of much less differentiated ZW sex chromosomes compared to chickens. To elucidate the evolution of chromosome architectures between ducks and chickens, and between birds and mammals, we produced a nearly complete chromosomal assembly of a female Pekin duck by combining long-read sequencing and multiplatform scaffolding techniques. RESULTS: A major improvement of genome assembly and annotation quality resulted from the successful resolution of lineage-specific propagated repeats that fragmented the previous Illumina-based assembly. We found that the duck topologically associated domains (TAD) are demarcated by putative binding sites of the insulator protein CTCF, housekeeping genes, or transitions of active/inactive chromatin compartments, indicating conserved mechanisms of spatial chromosome folding with mammals. There are extensive overlaps of TAD boundaries between duck and chicken, and also between the TAD boundaries and chromosome inversion breakpoints. This suggests strong natural selection pressure on maintaining regulatory domain integrity, or vulnerability of TAD boundaries to DNA double-strand breaks. The duck W chromosome retains 2.5-fold more genes relative to chicken. Similar to the independently evolved human Y chromosome, the duck W evolved massive dispersed palindromic structures, and a pattern of sequence divergence with the Z chromosome that reflects stepwise suppression of homologous recombination. CONCLUSIONS: Our results provide novel insights into the conserved and convergently evolved chromosome features of birds and mammals, and also importantly add to the genomic resources for poultry studies.
format Online
Article
Text
id pubmed-7787181
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77871812021-01-12 A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals Li, Jing Zhang, Jilin Liu, Jing Zhou, Yang Cai, Cheng Xu, Luohao Dai, Xuelei Feng, Shaohong Guo, Chunxue Rao, Jinpeng Wei, Kai Jarvis, Erich D Jiang, Yu Zhou, Zhengkui Zhang, Guojie Zhou, Qi Gigascience Research BACKGROUND: Ducks have a typical avian karyotype that consists of macro- and microchromosomes, but a pair of much less differentiated ZW sex chromosomes compared to chickens. To elucidate the evolution of chromosome architectures between ducks and chickens, and between birds and mammals, we produced a nearly complete chromosomal assembly of a female Pekin duck by combining long-read sequencing and multiplatform scaffolding techniques. RESULTS: A major improvement of genome assembly and annotation quality resulted from the successful resolution of lineage-specific propagated repeats that fragmented the previous Illumina-based assembly. We found that the duck topologically associated domains (TAD) are demarcated by putative binding sites of the insulator protein CTCF, housekeeping genes, or transitions of active/inactive chromatin compartments, indicating conserved mechanisms of spatial chromosome folding with mammals. There are extensive overlaps of TAD boundaries between duck and chicken, and also between the TAD boundaries and chromosome inversion breakpoints. This suggests strong natural selection pressure on maintaining regulatory domain integrity, or vulnerability of TAD boundaries to DNA double-strand breaks. The duck W chromosome retains 2.5-fold more genes relative to chicken. Similar to the independently evolved human Y chromosome, the duck W evolved massive dispersed palindromic structures, and a pattern of sequence divergence with the Z chromosome that reflects stepwise suppression of homologous recombination. CONCLUSIONS: Our results provide novel insights into the conserved and convergently evolved chromosome features of birds and mammals, and also importantly add to the genomic resources for poultry studies. Oxford University Press 2021-01-06 /pmc/articles/PMC7787181/ /pubmed/33406261 http://dx.doi.org/10.1093/gigascience/giaa142 Text en © The Author(s) 2021. Published by Oxford University Press GigaScience. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Li, Jing
Zhang, Jilin
Liu, Jing
Zhou, Yang
Cai, Cheng
Xu, Luohao
Dai, Xuelei
Feng, Shaohong
Guo, Chunxue
Rao, Jinpeng
Wei, Kai
Jarvis, Erich D
Jiang, Yu
Zhou, Zhengkui
Zhang, Guojie
Zhou, Qi
A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title_full A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title_fullStr A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title_full_unstemmed A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title_short A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
title_sort new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787181/
https://www.ncbi.nlm.nih.gov/pubmed/33406261
http://dx.doi.org/10.1093/gigascience/giaa142
work_keys_str_mv AT lijing anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhangjilin anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT liujing anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouyang anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT caicheng anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT xuluohao anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT daixuelei anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT fengshaohong anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT guochunxue anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT raojinpeng anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT weikai anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT jarviserichd anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT jiangyu anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouzhengkui anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhangguojie anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouqi anewduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT lijing newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhangjilin newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT liujing newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouyang newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT caicheng newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT xuluohao newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT daixuelei newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT fengshaohong newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT guochunxue newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT raojinpeng newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT weikai newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT jarviserichd newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT jiangyu newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouzhengkui newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhangguojie newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals
AT zhouqi newduckgenomerevealsconservedandconvergentlyevolvedchromosomearchitecturesofbirdsandmammals