Electrophoretic profile of sperm membrane proteins and correlation with fresh semen characteristics in Assam Hill goat


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Authors

  • S DEORI ICAR-NRC on Yak, Dirang, Arunachal Pradesh
  • B C DEKA Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • A ARANGASAMY Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • R K BISWAS Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • S SELVARAJU Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • D BHUYAN Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • N NAHARDEKA Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • L SOMASHEKAR Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • S PARTHIPAN Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • D J KALITA Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • RUMI SAIKIA BORAH Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India
  • ARUNDHATI PHOOKAN Assam Agricultural University, Khanapara, Guwahati, Asom 781 022 India

https://doi.org/10.56093/ijans.v86i11.63001

Keywords:

Correlation, Electrophoresis, Goat, Semen characteristics, Sperm membrane protein

Abstract

An experiment was carried out to study the electrophoretic profile of sperm membrane proteins in Assam Hill goat (AHG) bucks and their correlation with fresh semen characteristics. Ejaculates (64) consisting of 8 each from 8 bucks were collected by artificial vagina method. Each ejaculate was split into 2 equal parts. First part was used for fresh semen evaluation and the other part for protein study. Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS–PAGE) indicated 20 different protein bands with molecular weight ranging from 10 kDa to 75 kDa. Among the 20 proteins, only 6 proteins bands were consistently present in all 8 bucks (100%). Protein bands with molecular weight 10, 14, 22, 28, 55, 57 and 60 kDa showed significant positive correlation with certain parameters of the fresh semen, while 47 kDa protein band presented negative correlation with fresh semen characteristics in AHG bucks. In conclusion, the proteins showing significant positive correlation with fresh semen characteristics might serve to screen semen of AHG bucks for breeding programmes.

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References

Asadpour R, Alavi-Shoushtari S M, AsriRezaii S and Ansari M H. 2007. SDS-polyacrylamide gel electrophoresis of buffalo bulls seminal plasma proteins and their relation with semen freezability. Animal Reproduction Science 102: 308–13. DOI: https://doi.org/10.1016/j.anireprosci.2007.03.003

Blom E. 1977. Sperm morphology with reference to bull fertility. In: Proceedings of First All India Symposium on Animal Reproduction, Ludhiana, India.

Bradford M M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248–54. DOI: https://doi.org/10.1016/0003-2697(76)90527-3

Cancel A M, Chapman D A and Killian G J. 1997. Osteopontin is the 55–kilodalton fertility-associated protein in Holstein bull seminal plasma. Biology of Reproduction 57: 1293–1301. DOI: https://doi.org/10.1095/biolreprod57.6.1293

Cheema RS, Bhakri G, Vashishat N, Dhanju C K and Gandotra V K. 2011. SDS-PAGE of sperm membrane, epididymal tissue and fluid proteins of Indian mongrel: Identification and characterization of sperm specific proteins. International Journal of Innovations in Biological and Chemical Sciences 2: 22–34. DOI: https://doi.org/10.1177/205891581100200107

De Souza F F, Barreto C S and Lopes M D. 2007. Characteristics of seminal plasma proteins and their correlation with canine semen analysis. Theriogenology 68: 100–106. DOI: https://doi.org/10.1016/j.theriogenology.2006.11.016

Jeyendran R S, Van-Der-Ven H H, Perez-Pelaez M, Crabo B G and Zanevel L J. 1984. Development of an assay to assess the functional integrity of the human sperm membrane and its relationship to other semen characteristics. Journal of Reproduction and Fertility 70: 219–28. DOI: https://doi.org/10.1530/jrf.0.0700219

Karunakaran M, Devanathan T G, Jawahar T P, Manimaran K, Chitra A, Dhali A and Selvaraju S. 2012. Electrophoretic profile of bull sperm membrane proteins as a tool for selection of breeding bulls. Indian Journal of Animal Sciences 82: 1303– 05.

Killian G J, Chapman D A and Rogowski L A. 1993. Fertility– associated proteins in Holstein bull seminal plasma. Biology of Reproduction 49: 1202–07. DOI: https://doi.org/10.1095/biolreprod49.6.1202

Laemmli U K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680– 85. DOI: https://doi.org/10.1038/227680a0

Lovercamp K, Safranski T J, Fischer K A, Manandhar G, Sutovsky M, Herring W and Sutovsky P. 2007. Arachidonate 15– lipoxygenase and ubiquitin as fertility markers in boars. Theriogenology 67: 704–18. DOI: https://doi.org/10.1016/j.theriogenology.2006.08.019

Macanovic B, Vucetic M, Jankovic A, Stancic A, Buzadzic B, Garalejic E, Korac A, Korac B and Otasevic V. 2015. Correlation between sperm parameters and protein expression of antioxidative defense enzymes in seminal plasma: A pilot study. Disease Markers. DOI 10.1155/2015/436236. DOI: https://doi.org/10.1155/2015/436236

Nandi P, Ghosh S, Jana K and Sen PC. 2012. Elucidation of the involvement of p14, a sperm protein during maturation, capacitation and acrosome reaction of caprine spermatozoa. PLoS one. DOI 10.1371/ journal.pone.0030552. DOI: https://doi.org/10.1371/journal.pone.0030552

Schoneck C, Braun J and Einspanier R. 1996. Sperm viability is influenced in vitro by the bovine seminal protein aSFP: Effects on motility, mitochondrial activity and lipid peroxidation. Theriogenology 45: 633–42. DOI: https://doi.org/10.1016/0093-691X(95)00409-2

Sharma L, Pandey V, Nigam R, Saxena A and Swain D K. 2015. Association of semen attributes and seminal plasma proteins of buffalo bulls. Journal of Animal Research 5: 119–23. DOI: https://doi.org/10.5958/2277-940X.2015.00020.0

Snedecor G W and Cochran W G. 1994. Statistical Methods 8th edn. Iowa State University Press, Iowa.

Soubeyrand S, Khadir A, Brindle Y and Manjunath P. 1997. Purification of a novel phospholipase A2 from bovine seminal plasma. Journal of Biological Chemistry 272: 222–27. DOI: https://doi.org/10.1074/jbc.272.1.222

Teixeira A V C, Eloy A M X, Furtado J R, Pinheiro R R and Pontes M S. 2009. 1–D mapping of seminal plasma proteins in Anglo-Nubian goats. Animal Reproduction 6: 516–25.

Villemure M, Lazure C and Manjunath P. 2003. Isolation and characterization of gelatin–binding proteins from goat seminal plasma. Reproductive Biology and Endocrinology I: 39. Available from: http://www.RBEj.com/content/I/I/39 DOI: https://doi.org/10.1186/1477-7827-1-39

Watson P F. 1975. Use of a Giemsa stain to detect changes in acrosomes of frozen ram spermatozoa. Veterinary Record 97: 12–15. DOI: https://doi.org/10.1136/vr.97.1.12

Weinman S, Ores-Carton D, Rainteau D and Puszkin S. 1986. Immunoelectron microscopic localization of calmodulin and phospholipase A2 in spermatozoa. Journal of Histochemistry and Cytochemistry 34: 1171–79. DOI: https://doi.org/10.1177/34.9.2426345

Wolf D E and Voglmayr J K. 1984. Diffusion and regionalization in membranes of maturing ram spermatozoa. Journal of Cell Biology 98: 1678–84. DOI: https://doi.org/10.1083/jcb.98.5.1678

Yanagimachi R. 1994. Mammalian Fertilization. The Physiology of Reproduction. (Eds) Knobil E and Neill J D. pp. 189–317. Raven Press, New York.

Yuan Y Y, Chen W C, Shi Q X, Mao L M, Yu Q, Fang X and Roldan E R S. 2003. Zona pellucida induces activation of phospholipase A2 during acrosomal exocytosis in guinea pig spermatozoa. Biology of Reproduction 68: 904–13. DOI: https://doi.org/10.1095/biolreprod.102.005777

Yue W, Shi L, Bai Z, Ren Y and Zhoa Y. 2009. Sodium dodecyl sulfate (SDS) – polyacrylamide gel electrophoresis of ram seminal plasma proteins and their correlation with semen characteristics. Animal Reproduction Science 116: 386– 91. DOI: https://doi.org/10.1016/j.anireprosci.2009.02.014

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2016-11-11

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2016-11-28

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DEORI, S., DEKA, B. C., ARANGASAMY, A., BISWAS, R. K., SELVARAJU, S., BHUYAN, D., NAHARDEKA, N., SOMASHEKAR, L., PARTHIPAN, S., KALITA, D. J., BORAH, R. S., & PHOOKAN, A. (2016). Electrophoretic profile of sperm membrane proteins and correlation with fresh semen characteristics in Assam Hill goat. The Indian Journal of Animal Sciences, 86(11), 1269–1273. https://doi.org/10.56093/ijans.v86i11.63001
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