Changes in the Expression Profile of the Meiosis-Involved Mismatch Repair Genes in Impaired Human Spermatogenesis


Por: Terribas, E, Bonache, S, Garcia-Arevalo, M, Sanchez, J, Franco, E, Bassas, L, Larriba, S

Publicada: 1 jul 2010
Resumen:
DNA mismatch repair (MMR) genes have been described to participate in crossover events during meiotic recombination, which is, in turn, a key step of spermatogenesis. This evidence suggests that MMR family gene expression may be altered in infertile men with defective sperm production. In order to determine the expression profile of MMR genes in impaired human spermatogenesis, we performed transcript levels analysis of MMR genes (MLH1, MLH3, PMS2, MSH4, and MSH5), and other meiosis-involved genes (ATR, HSPA2, and SYCP3) as controls, by real-time reverse transcription polymerase chain reaction in testis from 13 patients with spermatogenic failure, 5 patients with primary germ cell tumors, and 10 controls with conserved spermatogenesis. Correlation of the expression values with the histological findings was also performed. The MMR gene expression values, with the exception of PMS2, are significantly decreased in men with spermatogenic failure. The pattern of MMR reduction correlates with the severity of damage, being maximum in maturation arrest. Specifically, expression of the testicular MSH4 gene could be useful as a surrogate marker for the presence of intratesticular elongated spermatid in patients with nonobstructive azoospermia, contributing to predict the viability of assisted reproduction. Interestingly, a reduction in the MSH4 and MSH5 transcript concentration per spermatocyte was also observed. The decreased expression level of other meiosis-specific genes, such as HSPA2 and SYCP3, suggests that the spermatocyte capacity to express meiosis-related genes is markedly reduced in spermatogenic failure, contributing to meiosis impairment and spermatogenic blockade.

Filiaciones:
Terribas, E:
 Hosp Duran & Reynals, Fundacio IDIBELL, Med & Mol Genet Ctr, Barcelona 08907, Spain

Bonache, S:
 Hosp Duran & Reynals, Fundacio IDIBELL, Med & Mol Genet Ctr, Barcelona 08907, Spain

Garcia-Arevalo, M:
 Hosp Duran & Reynals, Fundacio IDIBELL, Med & Mol Genet Ctr, Barcelona 08907, Spain

Sanchez, J:
 Fundacio Puigvert, Androl Serv, Barcelona, Spain

Franco, E:
 Hosp Univ Bellvitge, Urol Serv, Barcelona, Spain

Bassas, L:
 Fundacio Puigvert, Androl Serv, Barcelona, Spain

Larriba, S:
 Hosp Duran & Reynals, Fundacio IDIBELL, Med & Mol Genet Ctr, Barcelona 08907, Spain
ISSN: 01963635
Editorial
AMER SOC ANDROLOGY, INC, C/O ALLEN PRESS, INC PO BOX 368, LAWRENCE, KS 66044 USA, USA
Tipo de documento: Article
Volumen: 31 Número: 4
Páginas: 346-357
WOS Id: 000281875700004
ID de PubMed: 20075417
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