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Differential proteins associated with plasma membrane in X‐ and/or Y‐chromosome bearing spermatozoa in indicus cattle
Author(s) -
Laxmivandana Rongala,
Patole Chhaya,
Sharma Tilak Raj,
Sharma Kewal Krishan,
Naskar Soumen
Publication year - 2021
Publication title -
reproduction in domestic animals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.546
H-Index - 66
eISSN - 1439-0531
pISSN - 0936-6768
DOI - 10.1111/rda.13936
Subject(s) - semen , biology , sperm , capacitation , percoll , membrane protein , acrosome , andrology , proteomics , membrane , differential centrifugation , microbiology and biotechnology , gene , genetics , biochemistry , centrifugation , medicine
Abstract The differential proteins associated with plasma membrane of spermatozoa are less known, identification of which shall help overcome limitations of currently used methods of sperm sexing, considered as a high priority for livestock sector of many countries. This study has reported plasma membrane proteomics of unsorted spermatozoa and differential expression of plasma membrane‐associated proteins between X‐ and Y‐chromosome bearing spermatozoa of indicus cattle ( Bos indicus ). Isolation of plasma membrane fraction using percoll gradient, relatively a rapid method, from bovine spermatozoa has been reported to enrich isolation of plasma membrane proteins. Significant enrichment for plasma membrane‐associated proteins was observed in plasma membrane fraction ( p < .05) as compared to the total cell lysate using LC‐MS/MS. Furthermore, these experiments were conducted in flow cytometry sorted, sexed‐semen samples. Thirteen proteins were identified as differentially abundant between X‐ and Y‐sorted spermatozoa. Among these, two proteins were downregulated in Y‐sorted spermatozoa compared to the X‐sorted spermatozoa ( p < .05), while four and seven proteins could be noted in X‐ and Y‐sorted spermatozoa, respectively. Proteins that are presumed to support sperm capacitation and sperm migration velocity were found to be abundant in Y‐sorted spermatozoa while those associated with structural molecule activity were identified as abundant in X‐sorted spermatozoa in the present study. Our study provides better insight into the plasma membrane proteomics of spermatozoa of indicus cattle and furnishes data that might aid in design and development of alternate and open technology for sex‐sorting of semen.