Cargando…

Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot

Birds can be classified into altricial and precocial species. The hatchlings of altricial birds cannot stand, whereas precocial birds can walk and run soon after hatching. It might be owing to the development of the hindlimb bones in the embryo stage, but the molecular regulatory basis underlying th...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Qifan, Liu, Hehe, Yang, Qinglan, Wei, Bin, Wang, Luyao, Tang, Qian, Wang, Jianmei, Xi, Yang, Han, Chunchun, Wang, Jiwen, Li, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858812/
https://www.ncbi.nlm.nih.gov/pubmed/35198553
http://dx.doi.org/10.3389/fcell.2022.745129
_version_ 1784654317610860544
author Wu, Qifan
Liu, Hehe
Yang, Qinglan
Wei, Bin
Wang, Luyao
Tang, Qian
Wang, Jianmei
Xi, Yang
Han, Chunchun
Wang, Jiwen
Li, Liang
author_facet Wu, Qifan
Liu, Hehe
Yang, Qinglan
Wei, Bin
Wang, Luyao
Tang, Qian
Wang, Jianmei
Xi, Yang
Han, Chunchun
Wang, Jiwen
Li, Liang
author_sort Wu, Qifan
collection PubMed
description Birds can be classified into altricial and precocial species. The hatchlings of altricial birds cannot stand, whereas precocial birds can walk and run soon after hatching. It might be owing to the development of the hindlimb bones in the embryo stage, but the molecular regulatory basis underlying the divergence is unclear. To address this issue, we chose the altricial pigeon and the precocial Japanese quail as model animals. The data of tibia weight rate, embryonic skeletal staining, and tibia tissues paraffin section during the embryonic stage showed that the Japanese quail and pigeon have similar skeletal development patterns, but the former had a faster calcification rate. We utilized the comparative transcriptome approach to screen the genes and pathways related to this heterochronism. We separately analyzed the gene expression of tibia tissues of quail and pigeon at two consecutive time points from an inability to stand to be able to stand. There were 2910 differentially expressed genes (DEGs) of quail, and 1635 DEGs of pigeon, respectively. A total of 409 DEGs in common in the quail and pigeon. On the other hand, we compared the gene expression profiles of pigeons and quails at four time points, and screened out eight pairs of expression profiles with similar expression trends but delayed expression in pigeons. By screening the common genes in each pair of expression profiles, we obtained a gene set consisting of 152 genes. A total of 79 genes were shared by the 409 DEGs and the 152 genes. Gene Ontology analysis of these common genes showed that 21 genes including the COL gene family (COL11A1, COL9A3, COL9A1), IHH, MSX2, SFRP1, ATP6V1B1, SRGN, CTHRC1, NOG, and GDF5 involved in the process of endochondral ossification. These genes were the candidate genes for the difference of tibial development between pigeon and quail. This is the first known study on the embryo skeletal staining in pigeon. It provides some new insights for studying skeletal development mechanisms and locomotor ability of altricial and precocial bird species.
format Online
Article
Text
id pubmed-8858812
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88588122022-02-22 Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot Wu, Qifan Liu, Hehe Yang, Qinglan Wei, Bin Wang, Luyao Tang, Qian Wang, Jianmei Xi, Yang Han, Chunchun Wang, Jiwen Li, Liang Front Cell Dev Biol Cell and Developmental Biology Birds can be classified into altricial and precocial species. The hatchlings of altricial birds cannot stand, whereas precocial birds can walk and run soon after hatching. It might be owing to the development of the hindlimb bones in the embryo stage, but the molecular regulatory basis underlying the divergence is unclear. To address this issue, we chose the altricial pigeon and the precocial Japanese quail as model animals. The data of tibia weight rate, embryonic skeletal staining, and tibia tissues paraffin section during the embryonic stage showed that the Japanese quail and pigeon have similar skeletal development patterns, but the former had a faster calcification rate. We utilized the comparative transcriptome approach to screen the genes and pathways related to this heterochronism. We separately analyzed the gene expression of tibia tissues of quail and pigeon at two consecutive time points from an inability to stand to be able to stand. There were 2910 differentially expressed genes (DEGs) of quail, and 1635 DEGs of pigeon, respectively. A total of 409 DEGs in common in the quail and pigeon. On the other hand, we compared the gene expression profiles of pigeons and quails at four time points, and screened out eight pairs of expression profiles with similar expression trends but delayed expression in pigeons. By screening the common genes in each pair of expression profiles, we obtained a gene set consisting of 152 genes. A total of 79 genes were shared by the 409 DEGs and the 152 genes. Gene Ontology analysis of these common genes showed that 21 genes including the COL gene family (COL11A1, COL9A3, COL9A1), IHH, MSX2, SFRP1, ATP6V1B1, SRGN, CTHRC1, NOG, and GDF5 involved in the process of endochondral ossification. These genes were the candidate genes for the difference of tibial development between pigeon and quail. This is the first known study on the embryo skeletal staining in pigeon. It provides some new insights for studying skeletal development mechanisms and locomotor ability of altricial and precocial bird species. Frontiers Media S.A. 2022-02-07 /pmc/articles/PMC8858812/ /pubmed/35198553 http://dx.doi.org/10.3389/fcell.2022.745129 Text en Copyright © 2022 Wu, Liu, Yang, Wei, Wang, Tang, Wang, Xi, Han, Wang and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Wu, Qifan
Liu, Hehe
Yang, Qinglan
Wei, Bin
Wang, Luyao
Tang, Qian
Wang, Jianmei
Xi, Yang
Han, Chunchun
Wang, Jiwen
Li, Liang
Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title_full Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title_fullStr Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title_full_unstemmed Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title_short Developmental Transcriptome Profiling of the Tibial Reveals the Underlying Molecular Basis for Why Newly Hatched Quails Can Walk While Newly Hatched Pigeons Cannot
title_sort developmental transcriptome profiling of the tibial reveals the underlying molecular basis for why newly hatched quails can walk while newly hatched pigeons cannot
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858812/
https://www.ncbi.nlm.nih.gov/pubmed/35198553
http://dx.doi.org/10.3389/fcell.2022.745129
work_keys_str_mv AT wuqifan developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT liuhehe developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT yangqinglan developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT weibin developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT wangluyao developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT tangqian developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT wangjianmei developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT xiyang developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT hanchunchun developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT wangjiwen developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot
AT liliang developmentaltranscriptomeprofilingofthetibialrevealstheunderlyingmolecularbasisforwhynewlyhatchedquailscanwalkwhilenewlyhatchedpigeonscannot