Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells
Milk is important for human nutrition, and enhanced milk quality has become a major selection criterion for the genetic improvement of livestock. Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNA...
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description | Milk is important for human nutrition, and enhanced milk quality has become a major selection criterion for the genetic improvement of livestock. Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNAs are involved in the regulation of milk synthesis and in mammary gland development. Our study is the first to investigate the roles of miR‐29s and epigenetic regulation in dairy cow mammary epithelial cells (DCMECs). Our results show that miR‐29s regulate the DNA methylation level by inversely targeting both DNMT3A and DNMT3B in DCMECs. The inhibition of miR‐29s caused global DNA hypermethylation and increased the methylation levels of the promoters of important lactation‐related genes, including casein alpha s1 (CSN1S1), E74‐like factor 5 (ElF5), peroxisome proliferator‐activated receptor gamma (PPARγ), sterol regulatory element binding protein‐1 (SREBP1), and glucose transporter 1 (GLUT1). The inhibition of miR‐29s reduced the secretion of lactoprotein, triglycerides (TG) and lactose by DCMECs. Moreover, the treatment of DCMECs with 5‐aza‐2′‐deoxycytidine (5‐Aza‐dC) decreased the methylation levels of the miR‐29b promoter and increased the expression of miR‐29b. The link between miR‐29s and DNMT3A/3B enhances our understanding of the roles of miRNAs in mammary gland function, and our data will inform more experimentally oriented studies to identify new mechanisms of regulating lactation. We present new insights regarding the epigenetic regulation of lactation performance. Improved understanding of the molecular basis of lactation will aid in the development of strategies for optimizing milk quality in dairy cows and modifying the lactation performance of offspring. J. Cell. Physiol. 230: 2152–2163, 2015. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/jcp.24944 |
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Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNAs are involved in the regulation of milk synthesis and in mammary gland development. Our study is the first to investigate the roles of miR‐29s and epigenetic regulation in dairy cow mammary epithelial cells (DCMECs). Our results show that miR‐29s regulate the DNA methylation level by inversely targeting both DNMT3A and DNMT3B in DCMECs. The inhibition of miR‐29s caused global DNA hypermethylation and increased the methylation levels of the promoters of important lactation‐related genes, including casein alpha s1 (CSN1S1), E74‐like factor 5 (ElF5), peroxisome proliferator‐activated receptor gamma (PPARγ), sterol regulatory element binding protein‐1 (SREBP1), and glucose transporter 1 (GLUT1). The inhibition of miR‐29s reduced the secretion of lactoprotein, triglycerides (TG) and lactose by DCMECs. Moreover, the treatment of DCMECs with 5‐aza‐2′‐deoxycytidine (5‐Aza‐dC) decreased the methylation levels of the miR‐29b promoter and increased the expression of miR‐29b. The link between miR‐29s and DNMT3A/3B enhances our understanding of the roles of miRNAs in mammary gland function, and our data will inform more experimentally oriented studies to identify new mechanisms of regulating lactation. We present new insights regarding the epigenetic regulation of lactation performance. Improved understanding of the molecular basis of lactation will aid in the development of strategies for optimizing milk quality in dairy cows and modifying the lactation performance of offspring. J. Cell. Physiol. 230: 2152–2163, 2015. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.24944</identifier><identifier>PMID: 25656908</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>5-aza-2'-deoxycytidine ; Animals ; Azacytidine ; Casein ; Cattle ; Cow's milk ; Dairy cattle ; Deoxyribonucleic acid ; Development strategies ; DNA ; DNA (Cytosine-5-)-Methyltransferases - metabolism ; DNA methylation ; DNA Methylation - genetics ; Epigenesis, Genetic ; Epigenetics ; Epithelial cells ; Female ; Gene Expression Regulation ; Glucose transporter ; Human nutrition ; Humans ; Lactation ; Lactose ; Livestock ; Mammary gland ; Mammary Glands, Animal - metabolism ; MicroRNAs - antagonists & inhibitors ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Milk ; Milk - metabolism ; miRNA ; Nutrition ; Offspring ; Peroxisome proliferator-activated receptors ; Secretion ; Sterol regulatory element-binding protein ; Triglycerides</subject><ispartof>Journal of cellular physiology, 2015-09, Vol.230 (9), p.2152-2163</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4194-d8c663bec5cdd351e33dc9d314fa7c9d39a3ae507f6f64ae525701d1a907d9023</citedby><cites>FETCH-LOGICAL-c4194-d8c663bec5cdd351e33dc9d314fa7c9d39a3ae507f6f64ae525701d1a907d9023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.24944$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.24944$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25656908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bian, Yanjie</creatorcontrib><creatorcontrib>Lei, Yu</creatorcontrib><creatorcontrib>Wang, Chunmei</creatorcontrib><creatorcontrib>Wang, Jie</creatorcontrib><creatorcontrib>Wang, Lina</creatorcontrib><creatorcontrib>Liu, Lili</creatorcontrib><creatorcontrib>Liu, Lixin</creatorcontrib><creatorcontrib>Gao, Xuejun</creatorcontrib><creatorcontrib>Li, Qingzhang</creatorcontrib><title>Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells</title><title>Journal of cellular physiology</title><addtitle>J. Cell. Physiol</addtitle><description>Milk is important for human nutrition, and enhanced milk quality has become a major selection criterion for the genetic improvement of livestock. Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNAs are involved in the regulation of milk synthesis and in mammary gland development. Our study is the first to investigate the roles of miR‐29s and epigenetic regulation in dairy cow mammary epithelial cells (DCMECs). Our results show that miR‐29s regulate the DNA methylation level by inversely targeting both DNMT3A and DNMT3B in DCMECs. The inhibition of miR‐29s caused global DNA hypermethylation and increased the methylation levels of the promoters of important lactation‐related genes, including casein alpha s1 (CSN1S1), E74‐like factor 5 (ElF5), peroxisome proliferator‐activated receptor gamma (PPARγ), sterol regulatory element binding protein‐1 (SREBP1), and glucose transporter 1 (GLUT1). The inhibition of miR‐29s reduced the secretion of lactoprotein, triglycerides (TG) and lactose by DCMECs. Moreover, the treatment of DCMECs with 5‐aza‐2′‐deoxycytidine (5‐Aza‐dC) decreased the methylation levels of the miR‐29b promoter and increased the expression of miR‐29b. The link between miR‐29s and DNMT3A/3B enhances our understanding of the roles of miRNAs in mammary gland function, and our data will inform more experimentally oriented studies to identify new mechanisms of regulating lactation. We present new insights regarding the epigenetic regulation of lactation performance. Improved understanding of the molecular basis of lactation will aid in the development of strategies for optimizing milk quality in dairy cows and modifying the lactation performance of offspring. J. Cell. Physiol. 230: 2152–2163, 2015. © 2015 Wiley Periodicals, Inc.</description><subject>5-aza-2'-deoxycytidine</subject><subject>Animals</subject><subject>Azacytidine</subject><subject>Casein</subject><subject>Cattle</subject><subject>Cow's milk</subject><subject>Dairy cattle</subject><subject>Deoxyribonucleic acid</subject><subject>Development strategies</subject><subject>DNA</subject><subject>DNA (Cytosine-5-)-Methyltransferases - metabolism</subject><subject>DNA methylation</subject><subject>DNA Methylation - genetics</subject><subject>Epigenesis, Genetic</subject><subject>Epigenetics</subject><subject>Epithelial cells</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Glucose transporter</subject><subject>Human nutrition</subject><subject>Humans</subject><subject>Lactation</subject><subject>Lactose</subject><subject>Livestock</subject><subject>Mammary gland</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>MicroRNAs - antagonists & inhibitors</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Milk</subject><subject>Milk - metabolism</subject><subject>miRNA</subject><subject>Nutrition</subject><subject>Offspring</subject><subject>Peroxisome proliferator-activated receptors</subject><subject>Secretion</subject><subject>Sterol regulatory element-binding protein</subject><subject>Triglycerides</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhq0K1C6FA38AWeICh7Tjz8THVVpaYCnVClRulus4rbfJZokdyv57HNL2UKk9eSQ_82hmXoTeEjggAPRwZTcHlCvOd9CMgMozLgV9gWbpj2RKcLKHXoWwAgClGNtFe1RIIRUUM-SON_7KrV30Fi_d1dCY6Ls17mrc-mVGVcDzunY2BhyvHV4YGydgbqP_4-N2JI-M77e47G7xN9O2JtVJmvDGmwaXrmnCa_SyNk1wb-7effTz0_GP8jRbfD_5XM4XmeVE8awqrJTs0llhq4oJ4hirrKoY4bXJx0IZZpyAvJa15KmiIgdSEaMgrxRQto8-TN5N3_0eXIi69cGmCczadUPQRBYsF5wVkND3j9BVN_TrNJ0mSgKFdE75LJVcZKSKRH2cKNt3IfSu1pvej4fQBPSYkE4J6f8JJfbdnXG4bF31QN5HkoDDCbj1jds-bdJfyvN7ZTZ1-BDd34cO099omad99cXZiV6ekl8XFL7qc_YPWsqnUQ</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Bian, Yanjie</creator><creator>Lei, Yu</creator><creator>Wang, Chunmei</creator><creator>Wang, Jie</creator><creator>Wang, Lina</creator><creator>Liu, Lili</creator><creator>Liu, Lixin</creator><creator>Gao, Xuejun</creator><creator>Li, Qingzhang</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201509</creationdate><title>Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells</title><author>Bian, Yanjie ; Lei, Yu ; Wang, Chunmei ; Wang, Jie ; Wang, Lina ; Liu, Lili ; Liu, Lixin ; Gao, Xuejun ; Li, Qingzhang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4194-d8c663bec5cdd351e33dc9d314fa7c9d39a3ae507f6f64ae525701d1a907d9023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>5-aza-2'-deoxycytidine</topic><topic>Animals</topic><topic>Azacytidine</topic><topic>Casein</topic><topic>Cattle</topic><topic>Cow's milk</topic><topic>Dairy cattle</topic><topic>Deoxyribonucleic acid</topic><topic>Development strategies</topic><topic>DNA</topic><topic>DNA (Cytosine-5-)-Methyltransferases - metabolism</topic><topic>DNA methylation</topic><topic>DNA Methylation - genetics</topic><topic>Epigenesis, Genetic</topic><topic>Epigenetics</topic><topic>Epithelial cells</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Glucose transporter</topic><topic>Human nutrition</topic><topic>Humans</topic><topic>Lactation</topic><topic>Lactose</topic><topic>Livestock</topic><topic>Mammary gland</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>MicroRNAs - antagonists & inhibitors</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Milk</topic><topic>Milk - metabolism</topic><topic>miRNA</topic><topic>Nutrition</topic><topic>Offspring</topic><topic>Peroxisome proliferator-activated receptors</topic><topic>Secretion</topic><topic>Sterol regulatory element-binding protein</topic><topic>Triglycerides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bian, Yanjie</creatorcontrib><creatorcontrib>Lei, Yu</creatorcontrib><creatorcontrib>Wang, Chunmei</creatorcontrib><creatorcontrib>Wang, Jie</creatorcontrib><creatorcontrib>Wang, Lina</creatorcontrib><creatorcontrib>Liu, Lili</creatorcontrib><creatorcontrib>Liu, Lixin</creatorcontrib><creatorcontrib>Gao, Xuejun</creatorcontrib><creatorcontrib>Li, Qingzhang</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bian, Yanjie</au><au>Lei, Yu</au><au>Wang, Chunmei</au><au>Wang, Jie</au><au>Wang, Lina</au><au>Liu, Lili</au><au>Liu, Lixin</au><au>Gao, Xuejun</au><au>Li, Qingzhang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J. Cell. Physiol</addtitle><date>2015-09</date><risdate>2015</risdate><volume>230</volume><issue>9</issue><spage>2152</spage><epage>2163</epage><pages>2152-2163</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Milk is important for human nutrition, and enhanced milk quality has become a major selection criterion for the genetic improvement of livestock. Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNAs are involved in the regulation of milk synthesis and in mammary gland development. Our study is the first to investigate the roles of miR‐29s and epigenetic regulation in dairy cow mammary epithelial cells (DCMECs). Our results show that miR‐29s regulate the DNA methylation level by inversely targeting both DNMT3A and DNMT3B in DCMECs. The inhibition of miR‐29s caused global DNA hypermethylation and increased the methylation levels of the promoters of important lactation‐related genes, including casein alpha s1 (CSN1S1), E74‐like factor 5 (ElF5), peroxisome proliferator‐activated receptor gamma (PPARγ), sterol regulatory element binding protein‐1 (SREBP1), and glucose transporter 1 (GLUT1). The inhibition of miR‐29s reduced the secretion of lactoprotein, triglycerides (TG) and lactose by DCMECs. Moreover, the treatment of DCMECs with 5‐aza‐2′‐deoxycytidine (5‐Aza‐dC) decreased the methylation levels of the miR‐29b promoter and increased the expression of miR‐29b. The link between miR‐29s and DNMT3A/3B enhances our understanding of the roles of miRNAs in mammary gland function, and our data will inform more experimentally oriented studies to identify new mechanisms of regulating lactation. We present new insights regarding the epigenetic regulation of lactation performance. Improved understanding of the molecular basis of lactation will aid in the development of strategies for optimizing milk quality in dairy cows and modifying the lactation performance of offspring. J. Cell. Physiol. 230: 2152–2163, 2015. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25656908</pmid><doi>10.1002/jcp.24944</doi><tpages>12</tpages></addata></record> |
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subjects | 5-aza-2'-deoxycytidine Animals Azacytidine Casein Cattle Cow's milk Dairy cattle Deoxyribonucleic acid Development strategies DNA DNA (Cytosine-5-)-Methyltransferases - metabolism DNA methylation DNA Methylation - genetics Epigenesis, Genetic Epigenetics Epithelial cells Female Gene Expression Regulation Glucose transporter Human nutrition Humans Lactation Lactose Livestock Mammary gland Mammary Glands, Animal - metabolism MicroRNAs - antagonists & inhibitors MicroRNAs - genetics MicroRNAs - metabolism Milk Milk - metabolism miRNA Nutrition Offspring Peroxisome proliferator-activated receptors Secretion Sterol regulatory element-binding protein Triglycerides |
title | Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells |
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