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Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis

Fat-tail sheep exhibit a unique trait whereby substantial adipose tissue accumulates in the tail, a phenotype that is advantageous in many agroecological environments. In this study, we conducted histological assays, transcriptome analysis and functional assays to examine morphogenesis, characterize...

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Autores principales: Han, Jiangang, Ma, Sijia, Liang, Benmeng, Bai, Tianyou, Zhao, Yuhetian, Ma, Yuehui, MacHugh, David E., Ma, Lina, Jiang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957931/
https://www.ncbi.nlm.nih.gov/pubmed/35350385
http://dx.doi.org/10.3389/fcell.2022.839731
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author Han, Jiangang
Ma, Sijia
Liang, Benmeng
Bai, Tianyou
Zhao, Yuhetian
Ma, Yuehui
MacHugh, David E.
Ma, Lina
Jiang, Lin
author_facet Han, Jiangang
Ma, Sijia
Liang, Benmeng
Bai, Tianyou
Zhao, Yuhetian
Ma, Yuehui
MacHugh, David E.
Ma, Lina
Jiang, Lin
author_sort Han, Jiangang
collection PubMed
description Fat-tail sheep exhibit a unique trait whereby substantial adipose tissue accumulates in the tail, a phenotype that is advantageous in many agroecological environments. In this study, we conducted histological assays, transcriptome analysis and functional assays to examine morphogenesis, characterize gene expression, and elucidate mechanisms that regulate fat tail development. We obtained the microstructure of tail before and after fat deposition, and demonstrated that measurable fat deposition occurred by the 80-day embryo (E80) stage, earlier than other tissues. Transcriptome profiling revealed 1,058 differentially expressed genes (DEGs) with six markedly different expression trends. GSEA enrichment and other downstream analyses showed important roles for genes and pathways involving in metabolism and that mitochondrial components were specifically overexpressed in the fat tail tissue of the 70-day embryo (E70). One hundred and eighty-three genes were further identified by leading edge gene analysis, among which, 17 genes have been reported in previous studies, including EEF1D, MTFP1, PPP1CA, PDGFD. Notably, the MTFP1 gene was highly correlated with the expression of other genes and with the highest enrichment score and gene expression change. Knockdown of MTFP1 in isolated adipose derived stem cells (ADSCs) inhibited cell proliferation and migration ability, besides, promoted the process of adipogenesis in vitro.
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spelling pubmed-89579312022-03-28 Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis Han, Jiangang Ma, Sijia Liang, Benmeng Bai, Tianyou Zhao, Yuhetian Ma, Yuehui MacHugh, David E. Ma, Lina Jiang, Lin Front Cell Dev Biol Cell and Developmental Biology Fat-tail sheep exhibit a unique trait whereby substantial adipose tissue accumulates in the tail, a phenotype that is advantageous in many agroecological environments. In this study, we conducted histological assays, transcriptome analysis and functional assays to examine morphogenesis, characterize gene expression, and elucidate mechanisms that regulate fat tail development. We obtained the microstructure of tail before and after fat deposition, and demonstrated that measurable fat deposition occurred by the 80-day embryo (E80) stage, earlier than other tissues. Transcriptome profiling revealed 1,058 differentially expressed genes (DEGs) with six markedly different expression trends. GSEA enrichment and other downstream analyses showed important roles for genes and pathways involving in metabolism and that mitochondrial components were specifically overexpressed in the fat tail tissue of the 70-day embryo (E70). One hundred and eighty-three genes were further identified by leading edge gene analysis, among which, 17 genes have been reported in previous studies, including EEF1D, MTFP1, PPP1CA, PDGFD. Notably, the MTFP1 gene was highly correlated with the expression of other genes and with the highest enrichment score and gene expression change. Knockdown of MTFP1 in isolated adipose derived stem cells (ADSCs) inhibited cell proliferation and migration ability, besides, promoted the process of adipogenesis in vitro. Frontiers Media S.A. 2022-03-08 /pmc/articles/PMC8957931/ /pubmed/35350385 http://dx.doi.org/10.3389/fcell.2022.839731 Text en Copyright © 2022 Han, Ma, Liang, Bai, Zhao, Ma, MacHugh, Ma and Jiang. 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
Han, Jiangang
Ma, Sijia
Liang, Benmeng
Bai, Tianyou
Zhao, Yuhetian
Ma, Yuehui
MacHugh, David E.
Ma, Lina
Jiang, Lin
Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title_full Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title_fullStr Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title_full_unstemmed Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title_short Transcriptome Profiling of Developing Ovine Fat Tail Tissue Reveals an Important Role for MTFP1 in Regulation of Adipogenesis
title_sort transcriptome profiling of developing ovine fat tail tissue reveals an important role for mtfp1 in regulation of adipogenesis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957931/
https://www.ncbi.nlm.nih.gov/pubmed/35350385
http://dx.doi.org/10.3389/fcell.2022.839731
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