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Muscle Transcriptome Analysis of Mink at Different Growth Stages Using RNA-Seq
Mink is a kind of small and precious fur animal resource. In this study, we employed transcriptomics technology to analyze the gene expression profile of mink pectoral muscle tissue, thereby elucidating the regulatory mechanisms underlying mink growth and development. Consequently, a total of 25,954...
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Published in: | Biology (Basel, Switzerland) Switzerland), 2024-05, Vol.13 (5), p.283 |
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description | Mink is a kind of small and precious fur animal resource. In this study, we employed transcriptomics technology to analyze the gene expression profile of mink pectoral muscle tissue, thereby elucidating the regulatory mechanisms underlying mink growth and development. Consequently, a total of 25,954 gene expression profiles were acquired throughout the growth and development stages of mink at 45, 90, and 120 days. Among these profiles, 2607 genes exhibited significant differential expression (|log2(fold change)| ≥ 2 and
_adj < 0.05). GO and KEGG enrichment analyses revealed that the differentially expressed genes were primarily associated with the mitotic cell cycle process, response to growth factors, muscle organ development, and insulin resistance. Furthermore, GSEA enrichment analysis demonstrated a significant enrichment of differentially expressed genes in the p53 signaling pathway at 45 days of age. Subsequent analysis revealed that genes associated with embryonic development (e.g.,
,
,
), cell cycle regulation (e.g.,
,
,
,
), and the FGF family (e.g.,
,
,
) were all found to be upregulated at 45 days of age in mink, which suggested a potential role for these genes in governing early growth and developmental processes. Conversely, genes associated with skeletal muscle development (
,
,
,
,
), a negative regulator of the cell cycle gene (
), and
were found to be up-regulated at 90 days of age, suggesting their potential involvement in the rapid growth of mink. In summary, our experimental data provide robust support for elucidating the regulatory mechanisms underlying the growth and development of mink. |
doi_str_mv | 10.3390/biology13050283 |
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_adj < 0.05). GO and KEGG enrichment analyses revealed that the differentially expressed genes were primarily associated with the mitotic cell cycle process, response to growth factors, muscle organ development, and insulin resistance. Furthermore, GSEA enrichment analysis demonstrated a significant enrichment of differentially expressed genes in the p53 signaling pathway at 45 days of age. Subsequent analysis revealed that genes associated with embryonic development (e.g.,
,
,
), cell cycle regulation (e.g.,
,
,
,
), and the FGF family (e.g.,
,
,
) were all found to be upregulated at 45 days of age in mink, which suggested a potential role for these genes in governing early growth and developmental processes. Conversely, genes associated with skeletal muscle development (
,
,
,
,
), a negative regulator of the cell cycle gene (
), and
were found to be up-regulated at 90 days of age, suggesting their potential involvement in the rapid growth of mink. In summary, our experimental data provide robust support for elucidating the regulatory mechanisms underlying the growth and development of mink.</description><identifier>ISSN: 2079-7737</identifier><identifier>EISSN: 2079-7737</identifier><identifier>DOI: 10.3390/biology13050283</identifier><identifier>PMID: 38785766</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Age ; Animals ; Cell cycle ; Developmental stages ; Down-regulation ; Embryogenesis ; Fibroblast growth factor 2 ; Fibroblast growth factor 6 ; Fibroblast growth factor receptor 2 ; Fibroblast growth factors ; Gene expression ; Genes ; Genomes ; Genomics ; Growth ; Growth factors ; Insulin resistance ; Insulin-like growth factor II ; Insulin-like growth factor-binding protein 6 ; mink ; muscle development ; p53 Protein ; RNA ; RNA sequencing ; Signal transduction ; Skeletal muscle ; Small intestine ; Software ; Transcriptomes ; Transcriptomics</subject><ispartof>Biology (Basel, Switzerland), 2024-05, Vol.13 (5), p.283</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-a3a0224c4dc3ace11a029dea5d6b6243c5f145ec614c5e27914ef66dbbd119c33</citedby><cites>FETCH-LOGICAL-c471t-a3a0224c4dc3ace11a029dea5d6b6243c5f145ec614c5e27914ef66dbbd119c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3059386659/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3059386659?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38785766$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rong, Min</creatorcontrib><creatorcontrib>Xing, Xiumei</creatorcontrib><creatorcontrib>Zhang, Ranran</creatorcontrib><title>Muscle Transcriptome Analysis of Mink at Different Growth Stages Using RNA-Seq</title><title>Biology (Basel, Switzerland)</title><addtitle>Biology (Basel)</addtitle><description>Mink is a kind of small and precious fur animal resource. In this study, we employed transcriptomics technology to analyze the gene expression profile of mink pectoral muscle tissue, thereby elucidating the regulatory mechanisms underlying mink growth and development. Consequently, a total of 25,954 gene expression profiles were acquired throughout the growth and development stages of mink at 45, 90, and 120 days. Among these profiles, 2607 genes exhibited significant differential expression (|log2(fold change)| ≥ 2 and
_adj < 0.05). GO and KEGG enrichment analyses revealed that the differentially expressed genes were primarily associated with the mitotic cell cycle process, response to growth factors, muscle organ development, and insulin resistance. Furthermore, GSEA enrichment analysis demonstrated a significant enrichment of differentially expressed genes in the p53 signaling pathway at 45 days of age. Subsequent analysis revealed that genes associated with embryonic development (e.g.,
,
,
), cell cycle regulation (e.g.,
,
,
,
), and the FGF family (e.g.,
,
,
) were all found to be upregulated at 45 days of age in mink, which suggested a potential role for these genes in governing early growth and developmental processes. Conversely, genes associated with skeletal muscle development (
,
,
,
,
), a negative regulator of the cell cycle gene (
), and
were found to be up-regulated at 90 days of age, suggesting their potential involvement in the rapid growth of mink. In summary, our experimental data provide robust support for elucidating the regulatory mechanisms underlying the growth and development of mink.</description><subject>Age</subject><subject>Animals</subject><subject>Cell cycle</subject><subject>Developmental stages</subject><subject>Down-regulation</subject><subject>Embryogenesis</subject><subject>Fibroblast growth factor 2</subject><subject>Fibroblast growth factor 6</subject><subject>Fibroblast growth factor receptor 2</subject><subject>Fibroblast growth factors</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Growth</subject><subject>Growth factors</subject><subject>Insulin resistance</subject><subject>Insulin-like growth factor II</subject><subject>Insulin-like growth factor-binding protein 6</subject><subject>mink</subject><subject>muscle development</subject><subject>p53 Protein</subject><subject>RNA</subject><subject>RNA sequencing</subject><subject>Signal transduction</subject><subject>Skeletal muscle</subject><subject>Small intestine</subject><subject>Software</subject><subject>Transcriptomes</subject><subject>Transcriptomics</subject><issn>2079-7737</issn><issn>2079-7737</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUU1P3DAQtVCrgrace0OWeuklYMdfyXFFC0UCKhU4R449Tr1N4sV2VO2_x3QpqhhLM_bovWePH0KfKDllrCVnvQ9jGHaUEUHqhh2go5qotlKKqXf_7Q_RcUobUkKRWjL5AR2yRjVCSXmEbm-WZEbA91HPyUS_zWECvJ71uEs-4eDwjZ9_Y53xV-8cRJgzvozhT_6F77IeIOGH5OcB_7xdV3fw-BG9d3pMcPxSV-jh4tv9-ffq-sfl1fn6ujJc0Vxppkldc8OtYdoApeXYWtDCyl7WnBnhKBdgJOVGQK1aysFJafveUtoaxlboaq9rg9502-gnHXdd0L772whx6HTMvkzWOSBWcdeInlrOTdMoYYzQXInaiIaSovVlr7WN4XGBlLvJJwPjqGcIS-oYkYQp2RJVoJ_fQDdhieWznlGiZY2UJa_Q6R416HK_n13IUZuyLEzehBmcL_21agVTDeN1IZztCSaGlCK414ko6Z6t7t5YXRgnLw9Z-gnsK_6fsewJxG-jQg</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Rong, Min</creator><creator>Xing, Xiumei</creator><creator>Zhang, Ranran</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240501</creationdate><title>Muscle Transcriptome Analysis of Mink at Different Growth Stages Using RNA-Seq</title><author>Rong, Min ; Xing, Xiumei ; Zhang, Ranran</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-a3a0224c4dc3ace11a029dea5d6b6243c5f145ec614c5e27914ef66dbbd119c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Age</topic><topic>Animals</topic><topic>Cell cycle</topic><topic>Developmental stages</topic><topic>Down-regulation</topic><topic>Embryogenesis</topic><topic>Fibroblast growth factor 2</topic><topic>Fibroblast growth factor 6</topic><topic>Fibroblast growth factor receptor 2</topic><topic>Fibroblast growth factors</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Growth</topic><topic>Growth factors</topic><topic>Insulin resistance</topic><topic>Insulin-like growth factor II</topic><topic>Insulin-like growth factor-binding protein 6</topic><topic>mink</topic><topic>muscle development</topic><topic>p53 Protein</topic><topic>RNA</topic><topic>RNA sequencing</topic><topic>Signal transduction</topic><topic>Skeletal muscle</topic><topic>Small intestine</topic><topic>Software</topic><topic>Transcriptomes</topic><topic>Transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rong, Min</creatorcontrib><creatorcontrib>Xing, Xiumei</creatorcontrib><creatorcontrib>Zhang, Ranran</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biology (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rong, Min</au><au>Xing, Xiumei</au><au>Zhang, Ranran</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Muscle Transcriptome Analysis of Mink at Different Growth Stages Using RNA-Seq</atitle><jtitle>Biology (Basel, Switzerland)</jtitle><addtitle>Biology (Basel)</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>13</volume><issue>5</issue><spage>283</spage><pages>283-</pages><issn>2079-7737</issn><eissn>2079-7737</eissn><abstract>Mink is a kind of small and precious fur animal resource. In this study, we employed transcriptomics technology to analyze the gene expression profile of mink pectoral muscle tissue, thereby elucidating the regulatory mechanisms underlying mink growth and development. Consequently, a total of 25,954 gene expression profiles were acquired throughout the growth and development stages of mink at 45, 90, and 120 days. Among these profiles, 2607 genes exhibited significant differential expression (|log2(fold change)| ≥ 2 and
_adj < 0.05). GO and KEGG enrichment analyses revealed that the differentially expressed genes were primarily associated with the mitotic cell cycle process, response to growth factors, muscle organ development, and insulin resistance. Furthermore, GSEA enrichment analysis demonstrated a significant enrichment of differentially expressed genes in the p53 signaling pathway at 45 days of age. Subsequent analysis revealed that genes associated with embryonic development (e.g.,
,
,
), cell cycle regulation (e.g.,
,
,
,
), and the FGF family (e.g.,
,
,
) were all found to be upregulated at 45 days of age in mink, which suggested a potential role for these genes in governing early growth and developmental processes. Conversely, genes associated with skeletal muscle development (
,
,
,
,
), a negative regulator of the cell cycle gene (
), and
were found to be up-regulated at 90 days of age, suggesting their potential involvement in the rapid growth of mink. In summary, our experimental data provide robust support for elucidating the regulatory mechanisms underlying the growth and development of mink.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38785766</pmid><doi>10.3390/biology13050283</doi><oa>free_for_read</oa></addata></record> |
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subjects | Age Animals Cell cycle Developmental stages Down-regulation Embryogenesis Fibroblast growth factor 2 Fibroblast growth factor 6 Fibroblast growth factor receptor 2 Fibroblast growth factors Gene expression Genes Genomes Genomics Growth Growth factors Insulin resistance Insulin-like growth factor II Insulin-like growth factor-binding protein 6 mink muscle development p53 Protein RNA RNA sequencing Signal transduction Skeletal muscle Small intestine Software Transcriptomes Transcriptomics |
title | Muscle Transcriptome Analysis of Mink at Different Growth Stages Using RNA-Seq |
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