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Massachusetts Institute of Technology

The human Deleted in Azoospermia gene family : structure, function and evolution

Abstract

dc:description.abstract

The human Deleted in Azoospermia genes lie within the AZFc region of the Y chromosome that is frequently deleted in men with severe spermatogenic failure and male infertility. This thesis describes the evolution, structure and function of human DAZ genes. First, we determined that Y-linked DAZ genes arose by transposition from an autosomal ancestor during primate evolution, and were repeatedly amplified and pruned by multiple splicing mutations. This was the first example of acquisition of a male fertility factor by the Y chromosome independent of the X chromosome in any species. Then, we characterized the genomic structure and organization of four Y-linked DAZ genes in two clusters within the AZFc region. We found that each cluster has an inverted head to head pair of two DAZ genes. All DAZ genes appear capable of encoding DAZ proteins and two of these DAZ genes encode proteins with multimeric RNAbinding domains. We found transcripts from three DAZ genes. Next we determined the molecular nature of DAZ gene polymorphism in men. We deciphered 49f/a TaqI polymorphism, which corresponds to polymorphism in 2.4 kb repeats within all DAZ genes, and studied homogenization and deletion of one or the other DAZ gene cluster. We find that DAZ genes and corresponding DAZ proteins are highly polymorphic in different human Y chromosomal lineages. In the first appendix, we describe characterization of AZFc region deletions in three infertile men, two of whom have deletions of one DAZ cluster. In the second appendix, we describe partial rescue of the meiotic entry defect in Drosophila boule by overexpression of human DAZ and mouse DAZL proteins in testes of boule deficient flies. This functional assay suggests some functional conservation of DAZ and boule function. This thesis uncovers the genomic complexity, dynamic instability and evolution of a Y chromosomal gene family that is important for its role in human male fertility.

Degree

thesis:*
Department dc:contributor.department
Massachusetts Institute of Technology. Dept. of Biology.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2000

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Saxena, Richa, 1968-
Advisor dc:contributor.advisor
  • David C. Page.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/9021
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/9021

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Saxena, Richa, 1968-. The human Deleted in Azoospermia gene family : structure, function and evolution. Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/9021