Sperm mitochondrial-associated cysteine-rich protein is a protein that in humans is encoded by the SMCPgene.[1][2]
Function
Sperm mitochondria differ in morphology and subcellular localization from those of somatic cells. They are elongated, flattened, and arranged circumferentially to form a helical coiled sheath in the midpiece of the sperm flagellum. The protein encoded by this gene localizes to the capsule associated with the mitochondrial outer membranes and is thought to function in the organization and stabilization of the helical structure of the sperm's mitochondrial sheath.[2]
References
↑Aho H, Schwemmer M, Tessman D, Murphy D, Mattei G, Engel W, Adham IM (Mar 1996). "Isolation, expression, and chromosomal localization of the human mitochondrial capsule selenoprotein gene (MCSP)". Genomics. 32 (2): 184–90. doi:10.1006/geno.1996.0104. PMID8833144.
Karimpour I, Cutler M, Shih D, Smith J, Kleene KC (Nov 1992). "Sequence of the gene encoding the mitochondrial capsule selenoprotein of mouse sperm: identification of three in-phase TGA selenocysteine codons". DNA and Cell Biology. 11 (9): 693–9. doi:10.1089/dna.1992.11.693. PMID1418626.
Saaranen M, Suistomaa U, Vanha-Perttula T (Apr 1989). "Semen selenium content and sperm mitochondrial volume in human and some animal species". Human Reproduction. 4 (3): 304–8. doi:10.1093/oxfordjournals.humrep.a136893. PMID2715306.
Cataldo L, Baig K, Oko R, Mastrangelo MA, Kleene KC (Nov 1996). "Developmental expression, intracellular localization, and selenium content of the cysteine-rich protein associated with the mitochondrial capsules of mouse sperm". Molecular Reproduction and Development. 45 (3): 320–31. doi:10.1002/(SICI)1098-2795(199611)45:3<320::AID-MRD9>3.0.CO;2-U. PMID8916043.
Herr JC, Thomas D, Bush LA, Coonrod S, Khole V, Howards SS, Flickinger CJ (Aug 1999). "Sperm mitochondria-associated cysteine-rich protein (SMCP) is an autoantigen in Lewis rats". Biology of Reproduction. 61 (2): 428–35. doi:10.1095/biolreprod61.2.428. PMID10411523.
Yatsenko AN, Roy A, Chen R, Ma L, Murthy LJ, Yan W, Lamb DJ, Matzuk MM (Dec 2006). "Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization". Human Molecular Genetics. 15 (23): 3411–9. doi:10.1093/hmg/ddl417. PMID17047026.