DAZ family proteins exist throughout male germ cell development and transit from nucleus to cytoplasm at meiosis in humans and mice

Biology of Reproduction

Volumn 63, Issue 5, 2000, Pages 1490-1496

  Reijo, R A ^a   Dorfman, D M ^a   Slee, R ^a   Renshaw, A A ^a   Loughlin, K R ^a   Cooke, H ^a   Page, D C ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Sperm; Spermatogenesis

Indexed keywords

CELL PROTEIN;

ANIMAL TISSUE; ARTICLE; CELL NUCLEUS; CONTROLLED STUDY; CYTOPLASM; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INTRACELLULAR TRANSPORT; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN TRANSPORT; SPERMATID; SPERMATOGENESIS; SPERMATOZOON; Y CHROMOSOME;

ANIMALIA; DROSOPHILA; RODENTIA;

EID: 0033756262     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod63.5.1490     Document Type: Article

References (35)

1. Male infertility
2. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
3. Severe oligospermia resulting from deletions of the Azoospermia Factor gene on the Y chromosome
4. Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene
5. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
6. The Y chromosome region essential for spermatogenesis
7. Substantial prevalence of microdeletions of the Y-chromosome in infertile men with ideiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy
8. Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia
9. Microdeletions in the Y chromosome of infertile men
10. Microdeletions of the Y chromosome and intracytoplasmic sperm injection: From gene to clinic
11. Submicroscopic deletions in the Y chromosome of infertile men
12. Absence of DAZ gene mutations in cases of non-obstructed azoospermia
13. Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection
14. Y-chromosome deletions in idiopathic severe testiculopathies
15. Meiotic cell cycle requirement for a fly homologue of human Deleted in AZoospermia
16. The mouse Dazla gene encodes a cytoplasmic protein essential for gametogenesis
17. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned
18. A murine homologue of the human DAZ gene is autosomal and expressed only in male and female gonads
19. Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty
20. A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad
21. The human autosomal gene DAZLA: Testis specificity and a candidate for male infertility
22. Gene sequence, localization and evolution conservation of DAZLA, a candidate male sterility gene
23. cynDAZLA: A cynomolgus monkey homologue of the human autosomal DAZ gene
24. C. elegans homologue of DAZ/boule is involved in progression through meiosis during oogenesis
25. A Xenopus DAZ-like gene encodes an RNA component of germ plasm and is a functional homologue of Drosophila boule
26. Expression of DAZ, an azoospermia factor candidate, in human spermatogonia
27. In situ hybridization shows that Dazla expression in mouse testis is restricted to premeiotic stages IV-VI of spermatogenesis
28. Conserved structures and diversity of functions of RNA-binding proteins
29. Biphasic subcellular localization of the DAZL-related protein boule in Drosophila spermatogenesis
30. DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails
31. Cell biology of testicular development in the fetus and neonate
32. Spermatogonial stem cells
33. Cell biology of mammalian spermiogenesis
34. A human DAZ transgene confers partial rescue of the mouse DazlI null phenotype
35. The human DAZ genes, a putative male infertility factor on the Y chromosome, are highly polymorphic in the DAZ repeat regions