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MAMLD1 (CXorf6) is a New Gene for Hypospadias

MAMLD1 (mastermind-like domain containing 1), previously known as CXorf6 (chromosome X open reading frame 6), has been shown to be a causative gene for hypospadias. This is primarily based on the identification of nonsense mutations (E124X, Q197X, and R653X), which undergo nonsense mediated mRNA dec...

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Detalles Bibliográficos
Autores principales: Ogata, Tsutomu, Fukami, Maki, Wada, Yuka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004825/
https://www.ncbi.nlm.nih.gov/pubmed/24790369
http://dx.doi.org/10.1297/cpe.17.87
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author Ogata, Tsutomu
Fukami, Maki
Wada, Yuka
author_facet Ogata, Tsutomu
Fukami, Maki
Wada, Yuka
author_sort Ogata, Tsutomu
collection PubMed
description MAMLD1 (mastermind-like domain containing 1), previously known as CXorf6 (chromosome X open reading frame 6), has been shown to be a causative gene for hypospadias. This is primarily based on the identification of nonsense mutations (E124X, Q197X, and R653X), which undergo nonsense mediated mRNA decay, in patients with penoscrotal hypospadias. Subsequent molecular studies have shown that the mouse homolog is transiently expressed in fetal Sertoli and Leydig cells around the critical period for sex development, and that transient knockdown of Mamld1 results in significantly reduced testosterone production in murine Leydig tumor cells. These findings suggest that the MAMLD1 mutations cause hypospadias primarily because of compromised testosterone production around the critical period for sex development.
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spelling pubmed-40048252014-04-30 MAMLD1 (CXorf6) is a New Gene for Hypospadias Ogata, Tsutomu Fukami, Maki Wada, Yuka Clin Pediatr Endocrinol Review MAMLD1 (mastermind-like domain containing 1), previously known as CXorf6 (chromosome X open reading frame 6), has been shown to be a causative gene for hypospadias. This is primarily based on the identification of nonsense mutations (E124X, Q197X, and R653X), which undergo nonsense mediated mRNA decay, in patients with penoscrotal hypospadias. Subsequent molecular studies have shown that the mouse homolog is transiently expressed in fetal Sertoli and Leydig cells around the critical period for sex development, and that transient knockdown of Mamld1 results in significantly reduced testosterone production in murine Leydig tumor cells. These findings suggest that the MAMLD1 mutations cause hypospadias primarily because of compromised testosterone production around the critical period for sex development. The Japanese Society for Pediatric Endocrinology 2008-11-08 2008 /pmc/articles/PMC4004825/ /pubmed/24790369 http://dx.doi.org/10.1297/cpe.17.87 Text en 2008©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Review
Ogata, Tsutomu
Fukami, Maki
Wada, Yuka
MAMLD1 (CXorf6) is a New Gene for Hypospadias
title MAMLD1 (CXorf6) is a New Gene for Hypospadias
title_full MAMLD1 (CXorf6) is a New Gene for Hypospadias
title_fullStr MAMLD1 (CXorf6) is a New Gene for Hypospadias
title_full_unstemmed MAMLD1 (CXorf6) is a New Gene for Hypospadias
title_short MAMLD1 (CXorf6) is a New Gene for Hypospadias
title_sort mamld1 (cxorf6) is a new gene for hypospadias
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004825/
https://www.ncbi.nlm.nih.gov/pubmed/24790369
http://dx.doi.org/10.1297/cpe.17.87
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