MAP3K1, SPEF2 and PLCZ1 genes association with fertility and semen quality traits of AI bulls in Andhra Pradesh
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https://doi.org/10.56093/ijans.v94i7.149620
Keywords:
Association Buffalo, Cattle, Gene, Polymorphism, Semen quality, TraitAbstract
Bull fertility plays an important role in improving the economic value of the herd and is measured in terms of semen quality traits, which is influenced by both genetic and non-genetic factors. Polymorphism of MAP3K1/ CviQI (rs463712269), SPEF2/HpyCH4V (rs722354121) and PLCZ1/AvaII (rs208019489) and their association with scrotal circumference, sperm motility and plasma membrane integrity, respectively were studied on 239 bulls of different breeds reared in different frozen semen bull stations. The MAP3K1/CviQ1 assay revealed that T allele was more frequent in Ongole and Murrah population. RFLP at SPEF2/ HpyCH4V locus indicated fixation of T allele in both the exotic purebred cattle (Holstein Friesian and Jersey) whereas selective advantage of C allele was observed in Murrah buffaloes. Except in Holstein Friesian crossbred, other cattle genetic groups were with CC genotype for PLCZ1/AvaII assay and the Murrah population had low genetic diversity and heterozygosity excess. The PLCZ1/ AvaII genotypes had significant influence on the plasma membrane integrity of sperm in Holstein Friesian, Jersey and Ongole bulls. The plasma membrane integrity of sperm was reported to be high in heterozygotes (CG) of Jersey and Ongole cattle. The present study, concluded the importance of PLCZ1 gene as a marker for semen quality assessment and selection in bulls.
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Ahirwar M K, Kataktalware M A, Prasad K, Reen J K, Barman D, Pal R P and Gupta D. 2019. Digital infrared thermography as a tool to assess the effect of season, age and housing on seminal traits in Murrah bulls. Indian Journal of Animal Research 53: 1389–96.
Ahmad M and Asmat M T. 2005. Relationship of testicular size and libido to age and season in Sahiwal bulls. Pakistan Veterinary Journal 25: 67–70.
Atabay E P, Tadeo R D, Atabay E C, Venturina E V, Fissore R A and Mingala C N. 2018. Molecular characterization and comparison of phospholipase C zeta (PLCZ1) gene between swamp (Bubalus carabanensis) and riverine (Bubalus bubalis) buffaloes, its implications and future perspectives. Animal Biotechnology 29: 190–98.
Ballow D, Meistrich M L, Matzuk M and Rajkovic A. 2006. Sohlh1 is essential for spermatogonial differentiation. Developmental Biology 294(1): 161–67.
Berry D P, Wall E and Pryce J E. 2014. Genetics and genomics of reproductive performance in dairy and beef cattle. Animal 8105–21.
Bhave K G, Jawahar K T P, Kumarasamy P, Sivakumar T, Joseph C, Shirsath T and Venkataramanan R. 2020. Genetic and non-genetic factors affecting semen production and quality characteristics of Gir cattle breed under semi-arid climate. Veterinary World 13(8): 1714–18. doi:1014202/vetworld20201714-1718.
Boligon A A, Rorato P R N and Albuquerque L G D. 2007. Genetic correlations between scrotal perimeter measurements and productive and reproductive characteristics of Nellore females. Revista Brasileira de Zootecnia 36: 565–71.
Boujenane I and Boussaq K. 2013. Environmental effects and repeatability estimates for sperm production and semen quality of Holstein bulls. Archives Animal Breeding 56(1): 971–79. doi:107482/0003-9438-56-098.
Chakraborty S and Saha S. 2022. Understanding sperm motility mechanisms and the implication of sperm surface molecules in promoting motility. Middle East Fertility Society Journal 27(1). doi:101186/s43043-022-00094-7.
Crow J F and Kimura M. 2009. An Introduction to Population Genetics Theory. West Caldwell NJ: Blackburn Press.
Dejarnette J M, Marshall C E, Lenz R W, Monke D R, Ayars W H and Sattler C G. 2004. Sustaining the fertility of artificially inseminated dairy cattle, the role of the artificial insemination industry. Journal of Dairy Science 87: 93–104.
Druet T, Fritz S, Sellem E, Basso B, Gérard O, Salas-Cortes L and Eggen A. 2009. Estimation of genetic parameters and genome scan for 15 semen characteristics traits of Holstein bulls. Journal of Animal Breeding and Genetics 126(4): 269–77. doi:101111/j1439-0388200800788x.
Falconer D S. 1996. Introduction to Quantitative Genetics. Pearson Education, India.
Fuerst-Waltl B, Schwarzenbacher H, Perner C and Sölkner J. 2006. Effects of age and environmental factors on semen production and semen quality of Austrian Simmental bulls. Animal Reproduction Science 95(1–2): 27–37.
George D and Mallery P. 2019. IBM SPSS statistics 26 step by step, A simple guide and reference.
Ghoneimy M, Hasanain K, Youssef M, El-Menoufy Y, Sakr A and Mahdy A. 2017. Effect of body condition score and pcr- rflp polymorphism of prolactin gene on semen characteristics of buffalo bulls (Bubalus bubalis) prolactin gene on semen characteristics of buffalo bulls (Bubalus Bubalis). Egyptian Journal of Veterinary Sciences 48: 1–9.
Gopinathan Alagappan Sivaselvam S N, Kanniappan Karthickeyan S and Venkataramanan R. 2018a. Influence of non-genetic factors on semen quality parameters in crossbred jersey (Bos taurus × Bos indicus) bulls. International Journal of Current Microbiology and Applied Sciences 7(04): 2994–3004.
Gopinathan A, Sivaselvam S N, Karthickeyan S M K, Kulasekar K, Kirubaharan J J and Venkataramanan R. 2018b. Effect of non- genetic factors on semen quality traits of crossbred Holstein Friesian bulls (Bos taurus × Bos indicus) in organized farming conditions at Tamil Nadu, India. International Journal of Current Microbiology and Applied Sciences 7(11): 3219–29.
Gorbani A, Torshizi, R V, Bonyadi M and Amirinia C. 2009. A MspI PCR-RFLP within bovin growth hormone gene and its association with sperm quality traits in Iranian Holstein bulls. African Journal of Biotechnology 8.
Gredler B, Fuerst C, Fuerst-Waltl B, Schwarzenbacher H and Sölkner J. 2007. Genetic parameters for semen production traits in Austrian dual-purpose Simmental bulls Zucht hygiene. Reproduction in Domestic Animals 42(3): 326–28. doi:101111/j1439-0531200600778x.
Guo F, Yang B, Ju Z H, Wang X G, Qi C, Zhang Y and Huang J M. 2014. Alternative splicing, promoter methylation, and functional SNPs of sperm flagella 2 gene in testis and mature spermatozoa of Holstein bulls. Reproduction 147(2): 241–52. doi:101530/REP-13-0343.
Hahn J, Foote R H and Seidel G E Jr. 1969. Testicular growth and related sperm output in dairy bulls. Journal of Animal Science 29(1): 41–47. doi:102527/jas196929141x.
Hering D M, Olenski K and Kaminski S. 2014a. Genome-wide association study for sperm concentration in Holstein-Friesian bulls Zuchthygiene. Reproduction in Domestic Animals 49(6): 1008–14. doi:101111/rda12423.
Hering D M, Oleński K, Ruść A and Kaminski S. 2014b. Genome- wide association study for semen volume and total number of sperm in Holstein-Friesian bulls. Animal Reproduction Science 151(3–4): 126–30. doi:101016/janireprosci201410022.
Hildebrand C E, Torney D C and Wagner R P. 1992. Informativeness of polymorphic DNA markers. Los Alamos Science 20: 100–02.
Ishak A B L, Sumantri C, Noor R R and Arifiantini I. 2011. Identification of polymorphism of fsh beta-subunit gene as sperm quality marker in Bali cattle using PCR-RFLP. Journal of the Indonesian Tropical Animal Agriculture 36(4). doi:1014710/jitaa364221-227.
Jiang J, Liu L, Gao Y, Shi L, Li Y, Liang W and Sun D. 2019. Determination of genetic associations between indels in 11 candidate genes and milk composition traits in Chinese Holstein population. BMC Genetics 20: 48.
Kadri N K, Sahana G, Charlier C, Iso-Touru T, Guldbrandtsen B, Karim L and Druet T. 2014. A 660-Kb deletion with antagonistic effects on fertility and milk production segregates at high frequency in Nordic Red cattle, additional evidence for the common occurrence of balancing selection in livestock. PLoS Genetics 10.
Kenny D, Byrne C, English A M and Fair S. 2016. Bull fertility, important issues and current research. Open Day, Profitable Technologies Teagasc, Grange, Dunsany, Ireland. pp 138–41. Krovvidi S, Vinoo R, Metta M, Deepthi C, Surendra K and Jayamaduri B. 2021. Polymorphism of deleted in azoospermia- like (DAZL) gene in Ongole, Crossbred and Murrah bulls used for artificial insemination in Andhra Pradesh India. Indian Journal of Animal Research 11: 381–86.
Kumari S, Gupta I D, Verma A, Vineeth M R and Magotra A. 2017. Polymorphisms in exon 8 of bovine PLCZ1 gene and their association with semen quality in Sahiwal bulls. Ruminant Science 6: 201–06.
Liu X, Ju Z, Wang L, Zhang Y, Huang J, Li Q and Wang C. 2011. Six novel single-nucleotide polymorphisms in SPAG11 gene and their association with sperm quality traits in Chinese Holstein bulls. Animal Reproduction Science 129(1–2): 14–21. doi:101016/janireprosci201110003.
Mahmood S, Kumar A, Singh R, Sarkar M, Singh G, Verma M R and Kumar G V P P S R. 2018. Scrotal circumference A predictor of testosterone concentration and certain attributes of seminal vesicles influencing buffalo male fertility. Veterinary World 11.
Matabane M B, Thomas R, Netshirovha T R, Tsatsimpe M, Ng’ambi J W, Nephawe K A and Nedambale T L. 2017. Relationship between sperm plasma membrane integrity and morphology and fertility following artificial insemination. South African Journal of Animal Science 47(1): 102. doi:104314/sajasv47i115.
Mathevon M, Buhr M M and Dekkers J C. 1998. Environmental, management, and genetic factors affecting semen production in Holstein bulls. Journal of Dairy Science 81(12): 3321–30. doi:103168/jdsS0022-0302(98)75898-9.
McLaren W, Gil L, Hunt S E, Riat H S, Ritchie G R, Thormann A and Cunningham F. 2016. The ensembl variant effect predictor. Genome Biology 17(1): 1–14.
Meyer K, Hammond K, Mackinnon M J and Parnell P F. 1991. Estimates of covariances between reproduction and growth in Australian beef cattle. Journal of Animal Science 69(9): 3533–43. doi:102527/19916993533x.
Miah A G, Salma U, Sinha P B, Holker M, Tesfaye D, Cinar M U and Schellander K. 2011. Intracellular signaling cascades induced by relaxin in the stimulation of capacitation and acrosome reaction in fresh and frozen thawed bovine spermatozoa. Animal Reproduction Science 125: 30–41.
Mishra C, Palai T K, Sarangi L N, Prusty B R and Maharana B R. 2013. Candidate gene markers for sperm quality and fertility in bulls. Veterinary World 6(11): 905–10. doi:1014202/ vetworld2013905-910.
Montgomery G W and Sise J A. 1990. Extraction of DNA from sheep white blood cells. New Zealand Journal of Agricultural Research 33(3): 437–41. doi:101080/00288233199010428440.
Nikitkina E, Krutikova A, Musidray A and Plemyashov K. 2021. Search for associations of FSHR, INHA, INHAB, PRL, TNP2 and SPEF2 genes polymorphisms with semen quality in Russian Holstein bulls (pilot study). Animals: An Open Access Journal from MDPI 11(10). doi:103390/ ani11102882.
Pan, Q, Ju Z, Huang J, Zhang Y, Qi C, Gao Q and Wang C. 2013. PLCz functional haplotypes modulating promoter transcriptional activity are associated with semen quality traits in Chinese Holstein bulls. PloS One 8(3): e58795. doi:101371/ journalpone0058795.
Pearson K. 1990. On the criterion that a given system of deviations from the probable in the case of a correlated system of variables is such that it can be reasonably supposed to have arisen from random sampling. The London Edinburgh and Dublin Philosophical Magazine and Journal of Science 550: 157–75.
Perumal P, Savino N, Sangma C T R, Chang S, Sangtam T Z T, Khan M H and Srivastava N. 2017. Effect of season and age on scrotal circumference, testicular parameters and endocrinological profiles in mithun bulls. Theriogenology 98: 23–29.
Qin C, Yin H, Zhang X, Sun D, Zhang Q, Liu J and Zhang S. 2017. Genome-wide association study for semen traits of the bulls in Chinese Holstein. Animal Genetics 48(1): 80–84. doi:101111/age12433.
Quezada-Casasola A, Martínez-Armendáriz K E, Carrera-Chávez J M, Pérez-Eguía E, Rodríguez-Alarcón C A and Avendaño-Reyes L. 2016. Effect of season on scrotal circumference, semen characteristics and testosterone serum concentration in Mexican Corriente and other beef breed bulls. Animal Reproduction 13(4): 787–94. doi:1021451/1984-3143-ar805.
Raheja K L, Nadarajah K and Burnside E B. 1989. Relationship of bull fertility with daughter fertility and production traits in Holstein dairy cattle. Journal of Dairy Science 72(10): 2679–82. doi:103168/jdsS0022-0302(89)79409-1.
Rebecchi M J and Pentyala S N. 2000. Structure, function, and control of phosphoinositide-specific phospholipase C. Physiological Reviews 80(4): 1291–1335.
Ross P J, Beyhan Z, Iager A E, Yoon S-Y, Malcuit C, Schellander K and Cibelli J B. 2008. Parthenogenetic activation of bovine oocytes using bovine and murine phospholipase C zeta. BMC Developmental Biology 8(1): 16. doi:101186/1471-213X-8-16.
Sang L, Du Q-Z, Yang W-C, Tang K-Q, Yu J-N, Hua G-H and Yang L-G. 2011. Polymorphisms in follicle stimulation hormone receptor, inhibin alpha, inhibin bata A, and prolactin genes, and their association with sperm quality in Chinese Holstein bulls. Animal Reproduction Science 126(3–4): 151–56
Sato H, Taketomi Y, Isogai Y, Miki Y, Yamamoto K, Masuda S and Murakami M. 2010. Group III secreted phospholipase A2 regulates epididymal sperm maturation and fertility in mice. The Journal of Clinical Investigation 120(5): 1400– 1414. doi:101172/JCI40493.
Sironen A, Kotaja N, Mulhern H, Wyatt T A, Sisson J H, Pavlik J A and Lee L. 2011. Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia. Biology of Reproduction 85(4): 690–701. doi:101095/biolreprod111091132.
Sitanggang G. 2018. Pengaruh Lingkungan dan Nilai Ripitabilitas pada Kualitas Semen Sapi Peranakan Ongole Jantan. Jurnal Ilmu Pertanian Indonesia 23(2): 88–92.
Sun L-P, Du Q-Z, Song Y-P Yu J-N, Wang S-J, Sang L and Yang L-G. 2012. Polymorphisms in luteinizing hormone receptor and hypothalamic gonadotropin-releasing hormone genes and their effects on sperm quality traits in Chinese Holstein bulls. Molecular Biology Reports 39(6): 7117–23. doi:101007/s11033-012-1543-x.
Sweett H, Fonseca P A S, Suárez-Vega A, Livernois A, Miglior F and Cánovas A. 2020 Genome-wide association study to identify genomic regions and positional candidate genes associated with male fertility in beef cattle. Scientific Reports 10(1): 20102.
Tiwari A, Singh D, Kumar O S and Sharma M K .2008. Expression of cytochrome P450 aromatase transcripts in buffalo (Bubalus bubalis)-ejaculated spermatozoa and its relationship with sperm motility. Domestic Animal Endocrinology 34(3): 238–49. doi:101016/jdomaniend200707003.
Toelle V D and Robison O W. 1985. Estimates of genetic correlations between testicular measurements and female reproductive traits in cattle. Journal of Animal Science 60(1): 89–100. doi:102527/jas198560189x.
Van Melis M H, Eler J P, Rosa G J M, Ferraz J B S, Figueiredo L G G, Mattos E C and Oliveira H N. 2010. Additive genetic relationships between scrotal circumference, heifer pregnancy, and stayability in Nellore cattle. Journal of Animal Science 88(12): 3809–13. doi:102527/jas2009-2127.
Veerkamp R F and Beerda B. 2007. Genetics and genomics to improve fertility in high producing dairy cows. Theriogenology 68: S266–S273.
Vijay K, Abhijit B, Tejas S, Sameer J, Mahesh R, Kavita K and Hemant B. 2020. Association of semen traits in consecutive ejaculates with FSH-ß gene polymorphism in Holstein- Friesian crossbred bulls from India. Haryana Veterinarian 59: 38–40.
Wang J, Kimura E, Mongan M and Xia Y. 2021. Genetic control of MAP3K1 in eye development and sex differentiation. Cells (Basel, Switzerland) 11(1): 34 doi:103390/cells11010034.
Wu H, Smyth J, Luzzi V, Fukami K Takenawa T, Black S L and Fissore R A. 2001. Sperm factor induces intracellular free calcium oscillations by stimulating the phosphoinositide Pathway1. Biology of Reproduction 64(5): 1338–49.
Ye J, Coulouris G, Zaretskaya I, Cutcutache I, Rozen S and Madden T L. 2012. Primer-BLAST: A tool to design target- specific primers for polymerase chain reaction. BMC Bioinformatics 13: 1–11.
Yeh F C, Yang R and Boyle T. 1999. PopGene version 132 microsoft window–based freeware for population genetic analysis. University of Alberta Edmonton, AB, Canada.
Yue X P, Dechow C, Chang T C, Dejarnette J M, Marshall C E, Lei C Z and Liu W S. 2014. Copy number variations of the extensively amplified Y-linked genes, HSFY and ZNF280BY, in cattle and their association with male reproductive traits in Holstein bulls. BMC Genomics.
Zhang G W, Guan J Q, Luo Z G, Zhang W X, Wang L, Luo X L and Zuo F Y. 2016. A tremendous expansion of TSPY copy number in crossbred bulls (Bos taurus × Bos grunniens). Journal of Animal Science 94: 1398–1407.
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