Y Chromosome Infertility

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/y-chromosome-infertility

Y chromosome infertility is a condition that affects the production of sperm and causes male infertility, which means it is difficult or impossible for affected men to father children.

genetic conditions

1. Introduction

An affected man's body may produce no mature sperm cells (azoospermia), fewer than the usual number of sperm cells (oligospermia), or sperm cells that are abnormally shaped or that do not move properly. Men with Y chromosome infertility do not have any other signs or symptoms related to the condition.

Some men with Y chromosome infertility who have mild to moderate oligospermia may eventually father a child naturally. Men with oligospermia may also be helped with assisted reproductive technologies; most men with Y chromosome infertility have some sperm cells in the testes that can be extracted for this purpose.

2. Frequency

Y chromosome infertility occurs in approximately 1 in 2,000 to 1 in 3,000 males of all ethnic groups. This condition accounts for about 13 percent of cases of azoospermia and 5 percent of severe oligospermia.

3. Causes

As its name suggests, this form of infertility is caused by changes in the Y chromosome. People normally have 46 chromosomes in each cell. Two of the 46 chromosomes are sex chromosomes, called X and Y. Females have two X chromosomes (46,XX), and males have one X chromosome and one Y chromosome (46,XY).

Many genes on the Y chromosome are involved in male sex determination and development. In particular, genes in areas of the Y chromosome called azoospermia factor (AZF) regions provide instructions for making proteins that are involved in sperm cell production and development, although the specific functions of these proteins are not well understood.

Y chromosome infertility is caused by deletions of genes in the AZF regions. These deletions remove several genes, or in rare cases, a single gene. Loss of this genetic material likely prevents the production of one or more proteins needed for normal sperm cell development. As a result, either few sperm develop or sperm do not develop at all, leading to Y chromosome infertility.

4. Inheritance

Because Y chromosome infertility impedes the ability to father children, this condition is usually not inherited. Most cases of this condition result from new (de novo) deletions on the Y chromosome that occur during formation of sperm cells in an affected individual's father who is not himself infertile. These cases occur in men with no history of the disorder in their family.

When men with Y chromosome infertility do father children, either naturally or with the aid of assisted reproductive technologies, they pass the genetic changes on the Y chromosome to all their sons. As a result, the sons will also have Y chromosome infertility. This form of inheritance is called Y-linked. Daughters do not inherit the Y chromosome and are not affected.

5. Other Names for This Condition

spermatogenic failure, Y-linked
Y chromosome-related azoospermia

References

Esteves SC, Agarwal A. Novel concepts in male infertility. Int Braz J Urol.2011 Jan-Feb;37(1):5-15. Review.
Fan Y, Silber SJ. Y Chromosome Infertility. 2002 Oct 31 [updated 2019 Aug 1]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington,Seattle; 1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1339/
Gallego A, Rogel R, Luján S, Plaza B, Delgado F, Boronat F. AZF genemicrodeletions: case series and literature review. Actas Urol Esp. 2014Dec;38(10):698-702. doi: 10.1016/j.acuro.2014.04.003.English, Spanish.
Goncalves C, Cunha M, Rocha E, Fernandes S, Silva J, Ferraz L, Oliveira C,Barros A, Sousa M. Y-chromosome microdeletions in nonobstructive azoospermia and severe oligozoospermia. Asian J Androl. 2017 May-Jun;19(3):338-345. doi:10.4103/1008-682X.172827.
Krausz C, Casamonti E. Spermatogenic failure and the Y chromosome. Hum Genet. 2017 May;136(5):637-655. doi: 10.1007/s00439-017-1793-8.Review.
Liu XG, Hu HY, Guo YH, Sun YP. Correlation between Y chromosome microdeletion and male infertility. Genet Mol Res. 2016 Jun 3;15(2). doi: 10.4238/gmr.15028426.
Mau Kai C, Juul A, McElreavey K, Ottesen AM, Garn ID, Main KM, Loft A,Jørgensen N, Skakkebaek NE, Andersen AN, Rajpert-De Meyts E. Sons conceived byassisted reproduction techniques inherit deletions in the azoospermia factor(AZF) region of the Y chromosome and the DAZ gene copy number. Hum Reprod. 2008Jul;23(7):1669-78. doi: 10.1093/humrep/den124.
Pan Y, Zhang HG, Xi QI, Zhang H, Wang RX, Li LL, Liu RZ. Molecularmicrodeletion analysis of infertile men with karyotypic Y chromosomeabnormalities. J Int Med Res. 2018 Jan;46(1):307-315. doi:10.1177/0300060517719394.
Silber SJ. The Y chromosome in the era of intracytoplasmic sperm injection: a personal review. Fertil Steril. 2011 Jun 30;95(8):2439-48.e1-5. doi:10.1016/j.fertnstert.2011.05.070. Review.

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Bruce Ren

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Table of Contents

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1. Introduction

2. Frequency

3. Causes

4. Inheritance

5. Other Names for This Condition

References

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1. Introduction

2. Frequency

3. Causes

3.1 The chromosome associated with Y chromosome infertility

4. Inheritance

5. Other Names for This Condition

References