Differences during the first lactation between cows cloned by somatic cell nuclear transfer and noncloned cows

Lactation performance is dependent on both the genetic characteristics and the environmental conditions surrounding lactating cows. However, individual variations can still be observed within a given breed under similar environmental conditions. The role of the environment between birth and lactatio...

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Veröffentlicht in:Journal of dairy science 2016-06, Vol.99 (6), p.4778-4794
Hauptverfasser: Montazer-Torbati, F., Boutinaud, M., Brun, N., Richard, C., Neveu, A., Jaffrézic, F., Laloë, D., LeBourhis, D., Nguyen, M., Chadi, S., Jammes, H., Renard, J.-P., Chat, S., Boukadiri, A., Devinoy, E.
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container_issue 6
container_start_page 4778
container_title Journal of dairy science
container_volume 99
creator Montazer-Torbati, F.
Boutinaud, M.
Brun, N.
Richard, C.
Neveu, A.
Jaffrézic, F.
Laloë, D.
LeBourhis, D.
Nguyen, M.
Chadi, S.
Jammes, H.
Renard, J.-P.
Chat, S.
Boukadiri, A.
Devinoy, E.
description Lactation performance is dependent on both the genetic characteristics and the environmental conditions surrounding lactating cows. However, individual variations can still be observed within a given breed under similar environmental conditions. The role of the environment between birth and lactation could be better appreciated in cloned cows, which are presumed to be genetically identical, but differences in lactation performance between cloned and noncloned cows first need to be clearly evaluated. Conflicting results have been described in the literature, so our aim was to clarify this situation. Nine cloned Prim’ Holstein cows were produced by the transfer of nuclei from a single fibroblast cell line after cell fusion with enucleated oocytes. The cloned cows and 9 noncloned counterparts were raised under similar conditions. Milk production and composition were recorded monthly from calving until 200d in milk. At 67d in milk, biopsies were sampled from the rear quarter of the udder, their mammary epithelial cell content was evaluated, and mammary cell renewal, RNA, and DNA were then analyzed in relevant samples. The results showed that milk production did not differ significantly between cloned and noncloned cows, but milk protein and fat contents were less variable in cloned cows. Furthermore, milk fat yield and contents were lower in cloned cows during early lactation. At around 67 DIM, milk fat and protein yields, as well as milk fat, protein, and lactose contents, were also lower in cloned cows. These lower yields could be linked to the higher apoptotic rate observed in cloned cows. Apoptosis is triggered by insulin-like factor growth binding protein 5 (IGFBP5) and plasminogen activator inhibitor (PAI), which both interact with CSN1S2. During our experiments, CSN1S2 transcript levels were lower in the mammary gland of cloned cows. The mammary cell apoptotic rate observed in cloned cows may have been related to the higher levels of DNA (cytosine-5-)-methyltransferase 1 (DNMT1) transcripts, coding for products that maintain the epigenetic status of cells. We conclude, therefore, that milk production in cloned cows differs slightly from that of noncloned cows. These differences may be due, in part, to a higher incidence of subclinical mastitis. They were associated with differences in cell apoptosis and linked to variations in DNMT1 mRNA. However, milk protein and fat contents were more similar among cloned cows than among noncloned cows.
doi_str_mv 10.3168/jds.2015-10532
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However, individual variations can still be observed within a given breed under similar environmental conditions. The role of the environment between birth and lactation could be better appreciated in cloned cows, which are presumed to be genetically identical, but differences in lactation performance between cloned and noncloned cows first need to be clearly evaluated. Conflicting results have been described in the literature, so our aim was to clarify this situation. Nine cloned Prim’ Holstein cows were produced by the transfer of nuclei from a single fibroblast cell line after cell fusion with enucleated oocytes. The cloned cows and 9 noncloned counterparts were raised under similar conditions. Milk production and composition were recorded monthly from calving until 200d in milk. At 67d in milk, biopsies were sampled from the rear quarter of the udder, their mammary epithelial cell content was evaluated, and mammary cell renewal, RNA, and DNA were then analyzed in relevant samples. The results showed that milk production did not differ significantly between cloned and noncloned cows, but milk protein and fat contents were less variable in cloned cows. Furthermore, milk fat yield and contents were lower in cloned cows during early lactation. At around 67 DIM, milk fat and protein yields, as well as milk fat, protein, and lactose contents, were also lower in cloned cows. These lower yields could be linked to the higher apoptotic rate observed in cloned cows. Apoptosis is triggered by insulin-like factor growth binding protein 5 (IGFBP5) and plasminogen activator inhibitor (PAI), which both interact with CSN1S2. During our experiments, CSN1S2 transcript levels were lower in the mammary gland of cloned cows. The mammary cell apoptotic rate observed in cloned cows may have been related to the higher levels of DNA (cytosine-5-)-methyltransferase 1 (DNMT1) transcripts, coding for products that maintain the epigenetic status of cells. We conclude, therefore, that milk production in cloned cows differs slightly from that of noncloned cows. These differences may be due, in part, to a higher incidence of subclinical mastitis. They were associated with differences in cell apoptosis and linked to variations in DNMT1 mRNA. 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All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-f1e9d72283a5b3ee02298e0cdcec9669bb3026f6028788e329ff043fedafb1463</citedby><cites>FETCH-LOGICAL-c418t-f1e9d72283a5b3ee02298e0cdcec9669bb3026f6028788e329ff043fedafb1463</cites><orcidid>0000-0003-1488-4815 ; 0000-0001-8359-0760 ; 0000-0001-7579-6419 ; 0000-0003-0820-0966</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.3168/jds.2015-10532$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27016834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02635880$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Montazer-Torbati, F.</creatorcontrib><creatorcontrib>Boutinaud, M.</creatorcontrib><creatorcontrib>Brun, N.</creatorcontrib><creatorcontrib>Richard, C.</creatorcontrib><creatorcontrib>Neveu, A.</creatorcontrib><creatorcontrib>Jaffrézic, F.</creatorcontrib><creatorcontrib>Laloë, D.</creatorcontrib><creatorcontrib>LeBourhis, D.</creatorcontrib><creatorcontrib>Nguyen, M.</creatorcontrib><creatorcontrib>Chadi, S.</creatorcontrib><creatorcontrib>Jammes, H.</creatorcontrib><creatorcontrib>Renard, J.-P.</creatorcontrib><creatorcontrib>Chat, S.</creatorcontrib><creatorcontrib>Boukadiri, A.</creatorcontrib><creatorcontrib>Devinoy, E.</creatorcontrib><title>Differences during the first lactation between cows cloned by somatic cell nuclear transfer and noncloned cows</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><description>Lactation performance is dependent on both the genetic characteristics and the environmental conditions surrounding lactating cows. However, individual variations can still be observed within a given breed under similar environmental conditions. The role of the environment between birth and lactation could be better appreciated in cloned cows, which are presumed to be genetically identical, but differences in lactation performance between cloned and noncloned cows first need to be clearly evaluated. Conflicting results have been described in the literature, so our aim was to clarify this situation. Nine cloned Prim’ Holstein cows were produced by the transfer of nuclei from a single fibroblast cell line after cell fusion with enucleated oocytes. The cloned cows and 9 noncloned counterparts were raised under similar conditions. Milk production and composition were recorded monthly from calving until 200d in milk. At 67d in milk, biopsies were sampled from the rear quarter of the udder, their mammary epithelial cell content was evaluated, and mammary cell renewal, RNA, and DNA were then analyzed in relevant samples. 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Boutinaud, M. ; Brun, N. ; Richard, C. ; Neveu, A. ; Jaffrézic, F. ; Laloë, D. ; LeBourhis, D. ; Nguyen, M. ; Chadi, S. ; Jammes, H. ; Renard, J.-P. ; Chat, S. ; Boukadiri, A. ; Devinoy, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-f1e9d72283a5b3ee02298e0cdcec9669bb3026f6028788e329ff043fedafb1463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>Cloning, Organism</topic><topic>Dietary Fats - analysis</topic><topic>DNA (Cytosine-5-)-Methyltransferase 1</topic><topic>DNA (cytosine-5-)-methyltransferase 1 (DNMT1)</topic><topic>DNA (Cytosine-5-)-Methyltransferases - genetics</topic><topic>DNA (Cytosine-5-)-Methyltransferases - metabolism</topic><topic>Embryo Transfer - veterinary</topic><topic>Epigenesis, Genetic</topic><topic>epigenetics</topic><topic>Female</topic><topic>Insulin-Like Growth Factor Binding Protein 5 - genetics</topic><topic>Insulin-Like Growth Factor Binding Protein 5 - metabolism</topic><topic>Lactation</topic><topic>Lactose - analysis</topic><topic>Life Sciences</topic><topic>Mammary Glands, Animal - cytology</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Milk - chemistry</topic><topic>Milk - secretion</topic><topic>Milk Proteins - analysis</topic><topic>milk somatic cell counts</topic><topic>Plasminogen Inactivators - genetics</topic><topic>Plasminogen Inactivators - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>subclinical mastitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montazer-Torbati, F.</creatorcontrib><creatorcontrib>Boutinaud, M.</creatorcontrib><creatorcontrib>Brun, N.</creatorcontrib><creatorcontrib>Richard, C.</creatorcontrib><creatorcontrib>Neveu, A.</creatorcontrib><creatorcontrib>Jaffrézic, F.</creatorcontrib><creatorcontrib>Laloë, D.</creatorcontrib><creatorcontrib>LeBourhis, D.</creatorcontrib><creatorcontrib>Nguyen, M.</creatorcontrib><creatorcontrib>Chadi, S.</creatorcontrib><creatorcontrib>Jammes, H.</creatorcontrib><creatorcontrib>Renard, J.-P.</creatorcontrib><creatorcontrib>Chat, S.</creatorcontrib><creatorcontrib>Boukadiri, A.</creatorcontrib><creatorcontrib>Devinoy, E.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montazer-Torbati, F.</au><au>Boutinaud, M.</au><au>Brun, N.</au><au>Richard, C.</au><au>Neveu, A.</au><au>Jaffrézic, F.</au><au>Laloë, D.</au><au>LeBourhis, D.</au><au>Nguyen, M.</au><au>Chadi, S.</au><au>Jammes, H.</au><au>Renard, J.-P.</au><au>Chat, S.</au><au>Boukadiri, A.</au><au>Devinoy, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences during the first lactation between cows cloned by somatic cell nuclear transfer and noncloned cows</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>99</volume><issue>6</issue><spage>4778</spage><epage>4794</epage><pages>4778-4794</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><abstract>Lactation performance is dependent on both the genetic characteristics and the environmental conditions surrounding lactating cows. However, individual variations can still be observed within a given breed under similar environmental conditions. The role of the environment between birth and lactation could be better appreciated in cloned cows, which are presumed to be genetically identical, but differences in lactation performance between cloned and noncloned cows first need to be clearly evaluated. Conflicting results have been described in the literature, so our aim was to clarify this situation. Nine cloned Prim’ Holstein cows were produced by the transfer of nuclei from a single fibroblast cell line after cell fusion with enucleated oocytes. The cloned cows and 9 noncloned counterparts were raised under similar conditions. Milk production and composition were recorded monthly from calving until 200d in milk. At 67d in milk, biopsies were sampled from the rear quarter of the udder, their mammary epithelial cell content was evaluated, and mammary cell renewal, RNA, and DNA were then analyzed in relevant samples. 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subjects Animals
Apoptosis
Cattle
Cells, Cultured
Cloning, Organism
Dietary Fats - analysis
DNA (Cytosine-5-)-Methyltransferase 1
DNA (cytosine-5-)-methyltransferase 1 (DNMT1)
DNA (Cytosine-5-)-Methyltransferases - genetics
DNA (Cytosine-5-)-Methyltransferases - metabolism
Embryo Transfer - veterinary
Epigenesis, Genetic
epigenetics
Female
Insulin-Like Growth Factor Binding Protein 5 - genetics
Insulin-Like Growth Factor Binding Protein 5 - metabolism
Lactation
Lactose - analysis
Life Sciences
Mammary Glands, Animal - cytology
Mammary Glands, Animal - metabolism
Milk - chemistry
Milk - secretion
Milk Proteins - analysis
milk somatic cell counts
Plasminogen Inactivators - genetics
Plasminogen Inactivators - metabolism
RNA, Messenger - genetics
RNA, Messenger - metabolism
subclinical mastitis
title Differences during the first lactation between cows cloned by somatic cell nuclear transfer and noncloned cows
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