Regulation of CATSPER1 expression by the testis-determining gene SRY.
Aleida OlivaresAdriana Hernández-ReyesRicardo FelixÁngela ForeroMinerva Mata-RochaJavier Hernández-SánchezIsis SantosCharmina Aguirre-AlvaradoNorma OviedoPublished in: PloS one (2018)
CATSPER1 gene encodes a pore-forming and pH-sensing subunit of the CatSper Ca2+- permeable channel, a protein in the flagellum essential for sperm hyperactivation. Previous studies have shown that the murine Catsper1 gene promoter is regulated by different Sox proteins. Likewise, it is acknowledged that the human CATSPER1 gene promoter sequence is enriched in potential interaction sites for the sex-determining region Y gene (SRY), which suggest a novel regulatory transcriptional mechanism for CatSper1 channel expression. Therefore, in this work, we sought to determine whether the human CATSPER1 gene expression is regulated by the SRY transcription factor. To this end, a series of deletions and mutations were introduced in the wild- type CATSPER1 gene promoter to eliminate the SRY sites, and the different constructs were tested for their ability to activate transcription in human embryonic kidney and murine spermatogonial germ cell lines (HEK-293 and GC1-spg, respectively) using luciferase assays. In addition, by using a strategy that combines electrophoretic mobility shift assays (EMSA) and chromatin immunoprecipitation (ChIP) we investigated whether the CATSPER1 gene expression is regulated by the SRY transcription factor both in vitro and in vivo. Our results show that the transcriptional factor SRY specifically binds to different sites in the promoter sequence and has the ability to control CATSPER1 gene transcription.
Keyphrases
- transcription factor
- gene expression
- genome wide identification
- genome wide
- dna methylation
- copy number
- endothelial cells
- dna binding
- high throughput
- risk assessment
- dna damage
- genome wide analysis
- mass spectrometry
- stem cells
- binding protein
- long non coding rna
- climate change
- human health
- circulating tumor cells
- single cell
- case control