Study identifies new genetic cause of male reproductive birth defects

Baylor College of Medicine scientists defined a previously unrecognized genetic cause for two types of birth defects found in newborn boys, described in a report published today in the journal Nature Medicine.

"Cryptorchidism and hypospadias are among the most common birth defects but the causes are usually unknown," said Dr. Dolores Lamb, director of the Center for Reproductive Medicine at Baylor, professor and vice chair for research of urology and molecular and cellular biology at Baylor and lead author of the report.

Cryptorchidism is characterized by the failure of descent of one or both testes into the scrotum during fetal development. In the adult man, the testes produce sperm and the male hormone, testosterone. Hypospadias is the abnormal placement of the opening of the urethra on the penis. Both birth defects are usually surgically repaired during infancy.

Cryptorchidism occurs in about 3 percent of full term male births. Similarly, the incidence of hypospadias is about 1 in 125 births.

Lamb and colleagues used a method of genome wide screening (essentially a molecular karyotype) called array comparative genomic hybridization to study children with these defects. The method looks specifically at changes in chromosomal regions that have undergone duplication or deletions too small to see under a microscope, termed copy number variations. These genomic changes can alter gene dosage (gene gains or losses) resulting in a change in cell function.

In its analysis, the team showed that the cause of these birth defects in a subset of children with these defects of testis and penile development resulted from a change in the number of copies of a gene, VAMP7.

"The birth defects were a result of microduplication on the X chromosome that altered estrogen receptor and androgen receptor action in ways not previously recognized," said Lamb.

The interrelationship between androgen (such as testosterone, a steroid hormone that stimulates or controls the development and maintenance of male characteristics) and estrogen (the primary female sex hormone) working to regulate the differentiation of the male reproductive system relies on the balance between androgen and estrogen action, said the team.

The gene duplication occurred in 1.35 percent of the 324 patients studied, but was not present in nearly 9,000 control subjects who did not have these birth defects.

Accordingly, it is the most common known etiology to date, Lamb said. "This is far more common than androgen receptor mutations or defects in other known genes affecting testicular descent during development, such as INSL3."

The association of this gene duplication with the male reproductive tract birth defects was validated with mouse models that mimicked the human genomic duplication.

The Lamb laboratory observed the presence of the same birth defects in the mouse model as occurred in the children proving causation beyond an association.

The role of VAMP7 in causing these male birth defects was important because of the type of protein family it belongs to – it is a SNARE (Soluble N-ethylmaleimide-sensitive factor activating protein receptor) protein (a large protein superfamily consisting of more than 60 members in yeast and mammalian cell), Lamb said.

"This SNARE protein traffics the movement of other proteins in the cell. No one had ever considered that a minor change in the amount of this protein could so profoundly impact the and to a lesser extent androgen receptor action resulting in these male reproductive ."

The findings will help improve diagnosis and, hopefully, ultimately treatment, she said.

More information: Increased gene copy number of VAMP7 disrupts human male urogenital development through altered estrogen action, DOI: 10.1038/nm.3580

Related Stories

Mouse mutant opens new path for birth defect research

date Jan 16, 2013

(Medical Xpress)—According to the Centers for Disease Control, nearly 3 of every 100 babies in the U.S. are born with a birth defect. Among boys, one of the most common defects is the displacement of the ...

BPA linked to a common birth defect in boys

date Jun 17, 2013

A new study links fetal exposure to a common chemical pollutant, bisphenol A (BPA), to defects of a testicular hormone in newborn boys with undescended testicles. The results, which were presented Monday at The Endocrine ...

Recommended for you

Blood test may shed new light on Fragile X related disorders

date 13 hours ago

A blood test may shed new light on Fragile X syndrome related disorders in women, according to a new study published in the March 25, 2015, online issue of Neurology, the medical journal of the American Academy of Neurol ...

Recycling histones through transcription

date 17 hours ago

Cells reuse a part of the histones which are used to pack DNA, according to a current study by Karolinska Institutet. The study, which is published in the journal Genome Research, was conducted on yeast cells, but it is ...

User comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.