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PMID 17401724
Gene Name MTA1
Condition May be crucial for spermatogenesis
Association Associated
Sex Male
Infertility type Male infertility
Other associated phenotypes May be crucial for spermatogenesis


Correlation of appearance of metastasis-associated protein1 (Mta1) with spermatogenesis in developing mouse testis

Li W, Zhang J, Liu X, Xu R, Zhang Y.

Mta1, a representative of the MTA gene family, is believed to be involved in the metastasis of malignant tumors. However, a systematic study of its physiological function has not been performed. It has been found in normal mouse organs at relatively low levels, except for in testis, suggesting a potential function in the male reproductive system. In order to explore the role of Mta1 protein during spermatogenesis, its expression in adult mouse testis was compared with that in developing mouse testis and in testis from adult mice treated with methoxyacetic acid, which selectively depletes primary spermatocytes. Quantitative analysis revealed that Mta1 protein gradually increased in the testis from 14 days postnatally. Immunolocalization analysis demonstrated strong signals in the seminiferous tubules, and Mta1 was predominantly present in the nucleus of primary spermatocytes and spermatogonia from 14 days postnatally. The most intensive staining was located in the nucleus of pachytene spermatocytes in mature testes. The expression pattern of Mta1 during spermatogenesis was also shown to be stage-specific by immunohistochemistry analysis. Finally, dramatic loss of Mta1 expression from pachytene spermatocytes was observed in the spermatogenic-arrested adult mouse testis. These results collectively demonstrate that Mta1 appears during postnatal testis development and suggest that this expression may be crucial for spermatogenesis. FAU - Li, Wei AU - Li W AD - Department of Histology and Embryology, The Fourth Military Medical University, Xi'an, 710032, People's Republic of China. FAU - Zhang, Jinshan AU - Zhang J FAU - Liu, Xinping AU - Liu X FAU - Xu, Ruojun AU - Xu R