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Differential methylation status of IGF2-H19 locus does not affect the fertility of crossbred bulls but some of the CTCF binding sites could be potentially important
SUMMARY Associations between abnormal methylation of spermatozoan DNA with male infertility have been sought in recent years to identify a molecular explanation of differential spermatozoan function. The present work was undertaken to investigate the methylation profile of differentially methylated...
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Published in: | Molecular reproduction and development 2014-04, Vol.81 (4), p.350-362 |
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creator | Jena, Subas C. Kumar, Sandeep Rajput, Sandeep Roy, Bhaskar Verma, Arpana Kumaresan, Arumugam Mohanty, Tushar K. De, Sachinandan Kumar, Rakesh Datta, Tirtha K. |
description | SUMMARY
Associations between abnormal methylation of spermatozoan DNA with male infertility have been sought in recent years to identify a molecular explanation of differential spermatozoan function. The present work was undertaken to investigate the methylation profile of differentially methylated regions (DMRs) in the IGF2‐H19 locus of Bos taurus X Bos indicus crossbred bull spermatozoa. Bulls having more than at least 100 insemination records over a period of 12 years were classified into two groups of five bulls each belonging to low‐ and high‐fertility groups. The IGF2 and H19 DMR sequences in B. indicus cattle were observed to be in absolute homology with B. taurus cattle. The DNA of crossbred bull spermatozoa was isolated, bisulfite treated, and amplified for specific DMR regions using methylation‐change‐specific primers. The overall degree of methylation at IGF2‐H19 DMRs was not found to be significantly different among two groups of bulls. The sixth CTCF binding site (CCCTC) identified in H19 DMR, however, had a significant methylation difference between the high‐ and low‐fertility bulls. It was concluded that alteration of the methylation levels at IGF2‐H19 DMRs might not be responsible for the fertility difference of crossbred bulls, although the role played by the specific CTCF binding sites at this locus, which could influence IGF2 expression during spermatogenesis and early embryonic development, deserves further attention. Mol. Reprod. Dev. 81: 350–362, 2014. © 2014 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/mrd.22303 |
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Associations between abnormal methylation of spermatozoan DNA with male infertility have been sought in recent years to identify a molecular explanation of differential spermatozoan function. The present work was undertaken to investigate the methylation profile of differentially methylated regions (DMRs) in the IGF2‐H19 locus of Bos taurus X Bos indicus crossbred bull spermatozoa. Bulls having more than at least 100 insemination records over a period of 12 years were classified into two groups of five bulls each belonging to low‐ and high‐fertility groups. The IGF2 and H19 DMR sequences in B. indicus cattle were observed to be in absolute homology with B. taurus cattle. The DNA of crossbred bull spermatozoa was isolated, bisulfite treated, and amplified for specific DMR regions using methylation‐change‐specific primers. The overall degree of methylation at IGF2‐H19 DMRs was not found to be significantly different among two groups of bulls. The sixth CTCF binding site (CCCTC) identified in H19 DMR, however, had a significant methylation difference between the high‐ and low‐fertility bulls. It was concluded that alteration of the methylation levels at IGF2‐H19 DMRs might not be responsible for the fertility difference of crossbred bulls, although the role played by the specific CTCF binding sites at this locus, which could influence IGF2 expression during spermatogenesis and early embryonic development, deserves further attention. Mol. Reprod. Dev. 81: 350–362, 2014. © 2014 Wiley Periodicals, Inc.</description><identifier>ISSN: 1040-452X</identifier><identifier>EISSN: 1098-2795</identifier><identifier>DOI: 10.1002/mrd.22303</identifier><identifier>PMID: 24436206</identifier><identifier>CODEN: MREDEE</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; Binding Sites ; Bos indicus ; Bos taurus ; Cattle - genetics ; Cattle - physiology ; Cattle Diseases - genetics ; CCCTC-Binding Factor ; Crosses, Genetic ; Cryopreservation ; DNA - genetics ; DNA Methylation ; Female ; Hybridization, Genetic ; Infertility, Male - genetics ; Infertility, Male - veterinary ; Insulin-Like Growth Factor II - genetics ; Insulin-Like Growth Factor II - metabolism ; Male ; Pregnancy ; Pregnancy Rate ; Repressor Proteins - metabolism ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Semen Analysis ; Semen Preservation ; Sequence Homology, Nucleic Acid ; Spermatogenesis - genetics ; Spermatozoa - physiology ; Spermatozoa - ultrastructure</subject><ispartof>Molecular reproduction and development, 2014-04, Vol.81 (4), p.350-362</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4243-53c78ab99fe8f8dbea1c467447b31e3d86a7b45c89c8a9d3b476cdf5263d4ca93</citedby><cites>FETCH-LOGICAL-c4243-53c78ab99fe8f8dbea1c467447b31e3d86a7b45c89c8a9d3b476cdf5263d4ca93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24436206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jena, Subas C.</creatorcontrib><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Rajput, Sandeep</creatorcontrib><creatorcontrib>Roy, Bhaskar</creatorcontrib><creatorcontrib>Verma, Arpana</creatorcontrib><creatorcontrib>Kumaresan, Arumugam</creatorcontrib><creatorcontrib>Mohanty, Tushar K.</creatorcontrib><creatorcontrib>De, Sachinandan</creatorcontrib><creatorcontrib>Kumar, Rakesh</creatorcontrib><creatorcontrib>Datta, Tirtha K.</creatorcontrib><title>Differential methylation status of IGF2-H19 locus does not affect the fertility of crossbred bulls but some of the CTCF binding sites could be potentially important</title><title>Molecular reproduction and development</title><addtitle>Mol. Reprod. Dev</addtitle><description>SUMMARY
Associations between abnormal methylation of spermatozoan DNA with male infertility have been sought in recent years to identify a molecular explanation of differential spermatozoan function. The present work was undertaken to investigate the methylation profile of differentially methylated regions (DMRs) in the IGF2‐H19 locus of Bos taurus X Bos indicus crossbred bull spermatozoa. Bulls having more than at least 100 insemination records over a period of 12 years were classified into two groups of five bulls each belonging to low‐ and high‐fertility groups. The IGF2 and H19 DMR sequences in B. indicus cattle were observed to be in absolute homology with B. taurus cattle. The DNA of crossbred bull spermatozoa was isolated, bisulfite treated, and amplified for specific DMR regions using methylation‐change‐specific primers. The overall degree of methylation at IGF2‐H19 DMRs was not found to be significantly different among two groups of bulls. The sixth CTCF binding site (CCCTC) identified in H19 DMR, however, had a significant methylation difference between the high‐ and low‐fertility bulls. It was concluded that alteration of the methylation levels at IGF2‐H19 DMRs might not be responsible for the fertility difference of crossbred bulls, although the role played by the specific CTCF binding sites at this locus, which could influence IGF2 expression during spermatogenesis and early embryonic development, deserves further attention. Mol. Reprod. Dev. 81: 350–362, 2014. © 2014 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Binding Sites</subject><subject>Bos indicus</subject><subject>Bos taurus</subject><subject>Cattle - genetics</subject><subject>Cattle - physiology</subject><subject>Cattle Diseases - genetics</subject><subject>CCCTC-Binding Factor</subject><subject>Crosses, Genetic</subject><subject>Cryopreservation</subject><subject>DNA - genetics</subject><subject>DNA Methylation</subject><subject>Female</subject><subject>Hybridization, Genetic</subject><subject>Infertility, Male - genetics</subject><subject>Infertility, Male - veterinary</subject><subject>Insulin-Like Growth Factor II - genetics</subject><subject>Insulin-Like Growth Factor II - metabolism</subject><subject>Male</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><subject>Repressor Proteins - metabolism</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Semen Analysis</subject><subject>Semen Preservation</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Spermatogenesis - genetics</subject><subject>Spermatozoa - physiology</subject><subject>Spermatozoa - ultrastructure</subject><issn>1040-452X</issn><issn>1098-2795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkV1v1SAAhhujcXN64R8wJN7oRTe-2sKlnu2cbdlmYmY03hAK1DFpOQMa7f_xh0rXbRcmJrsBAs_7BHiL4jWC-whCfNAHvY8xgeRJsYsgZyVuePV0XlNY0gp_2ylexHgNIeScwefFDqaU1BjWu8WfQ9t1JpghWelAb9LV5GSyfgAxyTRG4Dtwslnj8hhx4LzKO9qbCAafgMxJlUC6MiArknU2TTOvgo-xDUaDdnQu5jGB6Hszn83w6nK1Bq0dtB1-gGhT1ik_uowbsPVpuYubgO23PiQ5pJfFs066aF7dzXvFl_XR5eq4PPu0OVl9OCsVxZSUFVENky3nnWEd062RSNG6obRpCTJEs1o2La0U44pJrklLm1rprsI10VRJTvaKd4t3G_zNaGISvY3KOCcH48coUIUhYazi5BEoqgnnEKOMvv0HvfZjGPJDZopySBCuMvV-oW5_L5hObIPtZZgEgmJuWeSWxW3LmX1zZxzb3ugH8r7WDBwswC_rzPR_kzj_fHivLJeEjcn8fkjI8FPUDWkq8fViI9D56Sle8-_iI_kLJwjBNw</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Jena, Subas C.</creator><creator>Kumar, Sandeep</creator><creator>Rajput, Sandeep</creator><creator>Roy, Bhaskar</creator><creator>Verma, Arpana</creator><creator>Kumaresan, Arumugam</creator><creator>Mohanty, Tushar K.</creator><creator>De, Sachinandan</creator><creator>Kumar, Rakesh</creator><creator>Datta, Tirtha K.</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>7QP</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201404</creationdate><title>Differential methylation status of IGF2-H19 locus does not affect the fertility of crossbred bulls but some of the CTCF binding sites could be potentially important</title><author>Jena, Subas C. ; Kumar, Sandeep ; Rajput, Sandeep ; Roy, Bhaskar ; Verma, Arpana ; Kumaresan, Arumugam ; Mohanty, Tushar K. ; De, Sachinandan ; Kumar, Rakesh ; Datta, Tirtha K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4243-53c78ab99fe8f8dbea1c467447b31e3d86a7b45c89c8a9d3b476cdf5263d4ca93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Binding Sites</topic><topic>Bos indicus</topic><topic>Bos taurus</topic><topic>Cattle - genetics</topic><topic>Cattle - physiology</topic><topic>Cattle Diseases - genetics</topic><topic>CCCTC-Binding Factor</topic><topic>Crosses, Genetic</topic><topic>Cryopreservation</topic><topic>DNA - genetics</topic><topic>DNA Methylation</topic><topic>Female</topic><topic>Hybridization, Genetic</topic><topic>Infertility, Male - genetics</topic><topic>Infertility, Male - veterinary</topic><topic>Insulin-Like Growth Factor II - genetics</topic><topic>Insulin-Like Growth Factor II - metabolism</topic><topic>Male</topic><topic>Pregnancy</topic><topic>Pregnancy Rate</topic><topic>Repressor Proteins - metabolism</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Semen Analysis</topic><topic>Semen Preservation</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Spermatogenesis - genetics</topic><topic>Spermatozoa - physiology</topic><topic>Spermatozoa - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jena, Subas C.</creatorcontrib><creatorcontrib>Kumar, Sandeep</creatorcontrib><creatorcontrib>Rajput, Sandeep</creatorcontrib><creatorcontrib>Roy, Bhaskar</creatorcontrib><creatorcontrib>Verma, Arpana</creatorcontrib><creatorcontrib>Kumaresan, Arumugam</creatorcontrib><creatorcontrib>Mohanty, Tushar K.</creatorcontrib><creatorcontrib>De, Sachinandan</creatorcontrib><creatorcontrib>Kumar, Rakesh</creatorcontrib><creatorcontrib>Datta, Tirtha K.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</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>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jena, Subas C.</au><au>Kumar, Sandeep</au><au>Rajput, Sandeep</au><au>Roy, Bhaskar</au><au>Verma, Arpana</au><au>Kumaresan, Arumugam</au><au>Mohanty, Tushar K.</au><au>De, Sachinandan</au><au>Kumar, Rakesh</au><au>Datta, Tirtha K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential methylation status of IGF2-H19 locus does not affect the fertility of crossbred bulls but some of the CTCF binding sites could be potentially important</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol. Reprod. Dev</addtitle><date>2014-04</date><risdate>2014</risdate><volume>81</volume><issue>4</issue><spage>350</spage><epage>362</epage><pages>350-362</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><coden>MREDEE</coden><abstract>SUMMARY
Associations between abnormal methylation of spermatozoan DNA with male infertility have been sought in recent years to identify a molecular explanation of differential spermatozoan function. The present work was undertaken to investigate the methylation profile of differentially methylated regions (DMRs) in the IGF2‐H19 locus of Bos taurus X Bos indicus crossbred bull spermatozoa. Bulls having more than at least 100 insemination records over a period of 12 years were classified into two groups of five bulls each belonging to low‐ and high‐fertility groups. The IGF2 and H19 DMR sequences in B. indicus cattle were observed to be in absolute homology with B. taurus cattle. The DNA of crossbred bull spermatozoa was isolated, bisulfite treated, and amplified for specific DMR regions using methylation‐change‐specific primers. The overall degree of methylation at IGF2‐H19 DMRs was not found to be significantly different among two groups of bulls. The sixth CTCF binding site (CCCTC) identified in H19 DMR, however, had a significant methylation difference between the high‐ and low‐fertility bulls. It was concluded that alteration of the methylation levels at IGF2‐H19 DMRs might not be responsible for the fertility difference of crossbred bulls, although the role played by the specific CTCF binding sites at this locus, which could influence IGF2 expression during spermatogenesis and early embryonic development, deserves further attention. Mol. Reprod. Dev. 81: 350–362, 2014. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24436206</pmid><doi>10.1002/mrd.22303</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Binding Sites Bos indicus Bos taurus Cattle - genetics Cattle - physiology Cattle Diseases - genetics CCCTC-Binding Factor Crosses, Genetic Cryopreservation DNA - genetics DNA Methylation Female Hybridization, Genetic Infertility, Male - genetics Infertility, Male - veterinary Insulin-Like Growth Factor II - genetics Insulin-Like Growth Factor II - metabolism Male Pregnancy Pregnancy Rate Repressor Proteins - metabolism RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Semen Analysis Semen Preservation Sequence Homology, Nucleic Acid Spermatogenesis - genetics Spermatozoa - physiology Spermatozoa - ultrastructure |
title | Differential methylation status of IGF2-H19 locus does not affect the fertility of crossbred bulls but some of the CTCF binding sites could be potentially important |
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