Characterization With Gene Mutations in Han Chinese Patients With Hypospadias and Function Analysis of a Novel AR Genevariant
It is estimated that around 10–20% of hypospadias are caused by genetic abnormalities worldwide although the spectrum of associated genes does vary across different ethnicities. The prevalence of hypospadias among the Chinese population has been increasing the last couple of decades. However, the pa...
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Published in | Frontiers in genetics Vol. 12; p. 673732 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
30.06.2021
|
Subjects | |
Online Access | Get full text |
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Summary: | It is estimated that around 10–20% of hypospadias are caused by genetic abnormalities worldwide although the spectrum of associated genes does vary across different ethnicities. The prevalence of hypospadias among the Chinese population has been increasing the last couple of decades. However, the pathogenesis underlying the disease and its associated genetic abnormality remains unclear. Here we performed a genetic analysis of 81 children with karyotype 46, XY and the hypospadias phenotype in order to characterize the genetic components that contribute to the development of hypospadias in Chinese patients. 15 candidate genes, including sex determination genes-
SOX9
,
SRY
,
NR0B1
(
DAX1
),
NR5A1
(
SF1
),
DHH
, sex differentiation genes
-AR
,
SRD5A2
,
MAMLD1
,
INSL3
, and hypospadias-associated genes
-FGF8
,
FGF10
,
BMP4
,
BMP7
,
ATF3
, and
MID1
were screened by using next generation sequencing. A total of 18 patients were found to have mutations identified by PCR and sequencing, including 11 cases of
SRD5A2
genes, 6 cases of
AR
genes, and 1 case of
MID1
gene, respectively. One novel missense mutation p.I817N was discovered in
AR
gene. Further molecular analysis found that subcellular localization of the AR
I
81
7N
was the same as that of wild type AR
WT
in the absence or presence of hormone. But it led to 50% reduction in AR-induced transcriptional activity in the presence of either the synthetic androgen R1881 or the natural ligand dihydrotestosterone. Our results indicate that
SRD5A2
and
AR
genes are two top candidate genes associated with 46, XY hypospadias in Chinese patients. Further epidemiological and genetic analysis are still needed to further clarify the pathogenesis of hypospadias in Han Chinese patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Aline L. Petrin, The University of Iowa, United States; Coriness Piñeyro-Ruiz, University of Puerto Rico, Medical Sciences Campus, Puerto Rico Edited by: Emiliano González Vioque, University Clinical Hospital of Santiago, Spain These authors have contributed equally to this work and share first authorship This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Genetics |
ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2021.673732 |