Bivalent 15 regularly associates with the sex vesicle in normal male meiosis
- PMID: 10515212
- DOI: 10.1023/a:1009268014387
Bivalent 15 regularly associates with the sex vesicle in normal male meiosis
Abstract
Using fluorescent in-situ hybridization, we investigated the positioning of different human bivalents at the pachytene stage of normal male meiosis. We showed that, in about 35% of nuclei, the pericentromeric region of bivalent 15 is closely associated with the sex vesicle (SV). This behaviour may be linked to the presence of three domains in the pericentromeric region of chromosome 15: a large imprinted domain, a nucleolar organizing region (NOR), and a heterochromatic block. In order to define the domains of chromosome 15 involved in this association, we analysed the meiotic behaviour of other bivalents with similar domains: human bivalent 11 and mouse bivalent 7, bearing imprinted domains, other human acrocentric bivalents bearing a NOR, and the human bivalents 1, 9 and 16 containing a heterochromatic region. None of these bivalents were as frequently associated with the SV as the human bivalent 15. Nevertheless, we suggest that the bivalent 15 heterochromatin may be responsible for the association because of two properties: its telomeric location on chromosome 15 and its strong sequence homology with the Yq heterochromatin. This phenomenon could explain the high frequency of translocations between the chromosome 15 and the X or Y chromosomes.
Similar articles
-
Nuclear architecture of human pachytene spermatocytes: quantitative analysis of associations between nucleolar and XY bivalents.Hum Genet. 1990 Dec;86(2):103-16. doi: 10.1007/BF00197690. Hum Genet. 1990. PMID: 2265823
-
The association of the nucleolus and the short arm of acrocentric chromosomes with the XY pair in human spermatocytes: its possible role in facilitating sex-chromosome acrocentric translocations.Hum Genet. 1984;68(2):173-80. doi: 10.1007/BF00279310. Hum Genet. 1984. PMID: 6500568
-
Sex vesicle-associated nucleolar organizers in mouse spermatocytes: localization, structure, and function.Cytogenet Cell Genet. 1981;31(2):47-57. doi: 10.1159/000131625. Cytogenet Cell Genet. 1981. PMID: 7307582
-
XY chromosomal bivalent: nucleolar attraction.Mol Reprod Dev. 2005 Sep;72(1):1-6. doi: 10.1002/mrd.20334. Mol Reprod Dev. 2005. PMID: 15915516 Review.
-
Nuclear Architecture of Mouse Spermatocytes: Chromosome Topology, Heterochromatin, and Nucleolus.Cytogenet Genome Res. 2017;151(2):61-71. doi: 10.1159/000460811. Epub 2017 May 12. Cytogenet Genome Res. 2017. PMID: 28494440 Review.
Cited by
-
Small Supernumerary Marker Chromosome (sSMC) 15 in Male Primary Infertility: A Case Study.Case Rep Med. 2025 Apr 23;2025:9935363. doi: 10.1155/carm/9935363. eCollection 2025. Case Rep Med. 2025. PMID: 40313645 Free PMC article.
-
Prenatal diagnosis of the maternal derivative chromosome der(15)t(Y;15)(q12;p13) in a dizygotic twin pregnancy.Tzu Chi Med J. 2016 Oct-Dec;28(4):176-179. doi: 10.1016/j.tcmj.2016.06.002. Epub 2016 Jul 2. Tzu Chi Med J. 2016. PMID: 28757753 Free PMC article.
-
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.J Assist Reprod Genet. 2020 Jul;37(7):1729-1736. doi: 10.1007/s10815-020-01811-9. Epub 2020 May 12. J Assist Reprod Genet. 2020. PMID: 32399795 Free PMC article. Review.
-
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient.Sci Rep. 2015 Nov 30;5:17408. doi: 10.1038/srep17408. Sci Rep. 2015. PMID: 26616419 Free PMC article.
-
HP1beta and HP1gamma, but not HP1alpha, decorate the entire XY body during human male meiosis.Chromosome Res. 2003;11(1):73-81. doi: 10.1023/a:1022014217196. Chromosome Res. 2003. PMID: 12675308
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources