Literature DB >> 26406169

Functional Characterization of c.870+3_6delGAGT Splice Site Mutation in NR5A1.

Masaki Takagi1, Noriko Nishina, Hiroko Yagi, Yukihiro Hasegawa.   

Abstract

BACKGROUND: To date, more than 100 mutations of NR5A1 have been reported; however, mutations affecting the splice site are rare, with only two reported mutations.
OBJECTIVE: To characterize the c.870+3_6delGAGT splice mutation of NR5A1 through molecular analyses.
RESULTS: The reverse transcription polymerase chain reaction (RT-PCR) study revealed that c.870+3_6delGAGT resulted in p.A82fs*95. Mutant NR5A1 showed a reduced transactivation on the CYP11A1 and STAR promoters without a dominant negative effect.
CONCLUSION: To the best of our knowledge, this is the first report of the NR5A1 splice site mutation, which was proven to be deleterious by the RT-PCR method.
© 2015 S. Karger AG, Basel.

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Year:  2015        PMID: 26406169     DOI: 10.1159/000440862

Source DB:  PubMed          Journal:  Horm Res Paediatr        ISSN: 1663-2818            Impact factor:   2.852


  1 in total

1.  Two Unrelated Undervirilized 46,XY Males with Inherited NR5A1 Variants Identified by Whole-Exome Sequencing.

Authors:  Jonathan M Swartz; Ryan Ciarlo; Michael H Guo; Aser Abrha; David A Diamond; Yee-Ming Chan; Joel N Hirschhorn
Journal:  Horm Res Paediatr       Date:  2016-08-24       Impact factor: 2.852

  1 in total

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