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Underexpression of hsa-miR-449 family and their promoter hypermethylation in infertile men: A case-control study

BACKGROUND: Post-transcriptional microRNAs (miRNAs) have a impotrant pattern in the spermatogenesis process. OBJECTIVE: Study of the expression and methylation of hsa-miR-449 family in sperm samples of infertile men. MATERIALS AND METHODS: In this case-control study, we recruited 74 infertile men (w...

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Detalles Bibliográficos
Autores principales: Najafipour, Reza, Momeni, Abdolmabood, Yousefipour, Farideh, Mousavi, Shaghayegh, Moghbelinejad, Sahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851476/
https://www.ncbi.nlm.nih.gov/pubmed/33554000
http://dx.doi.org/10.18502/ijrm.v19i1.8177
Descripción
Sumario:BACKGROUND: Post-transcriptional microRNAs (miRNAs) have a impotrant pattern in the spermatogenesis process. OBJECTIVE: Study of the expression and methylation of hsa-miR-449 family in sperm samples of infertile men. MATERIALS AND METHODS: In this case-control study, we recruited 74 infertile men (with asthenozoospermia, teratozoospermia, asthenoteratozoospermia, and oligoasthenoteratozoospermia) and 30 control samles. Methylation-specific PCR (MSP) method was used for methylation evaluation of hsa-miR-449 a, b, c promoter. By Real time PCR (qRT-PCR) method,we showed downregulation of hsa-miR-449 a, b, c in the sperm samples of infertile men and compared it to their fertile counterparts. RESULTS: There was significant underexperssion, in hsa-miR-449-b in oligoasthenoteratospermic samples (p = 0.0001, F = 2.9). About the methylation pattern, infertile men showed high frequency of methylation in the promoter of hsa-miR-449 a, b, c in comparison to controls (60.8% vs 23.3%), the highest amount of methylation was observed in oligoasthenoteratospermia samples (81.2%). CONCLUSION: In this study, low expression and high methylation of hsa-miR-449-b were observed in infertile men in compared to control samples, which can be one of the causes of defective spermatogenesis.