» Articles » PMID: 3698745

Loop Formation and Synaptic Adjustment in a Human Male Heterozygous for Two Pericentric Inversions

Overview
Journal Chromosoma
Specialty Molecular Biology
Date 1986 Jan 1
PMID 3698745
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Pachytene analysis was undertaken in an infertile male heterozygous for two pericentric inversions of chromosomes 1 and 9. The synaptic behaviour of the bivalent 1 inversion was the most informative. Analysis of the chromomere pattern combined with centromeric heterochromatin staining allowed precise description of synaptic initiation and extension leading to the homosynapsed loop. These techniques also allowed demonstration of the existence of heterosynapsis following alignment of the inverted segments. Non-homologous synapsed bivalents had the morphological aspects of straight bivalents with two distant blocks of centromeric heterochromatin. The numbering of the autosomal bivalent chromomeres at various successive phases of the inversion loop behaviour of bivalent 1 permitted us an alternative approach to the timing of pachytene.

Citing Articles

Formation and resolution of meiotic chromosome entanglements and interlocks.

Olaya I, Burgess S, Rog O J Cell Sci. 2024; 137(13).

PMID: 38985540 PMC: 11267460. DOI: 10.1242/jcs.262004.


Pericentric inversion in chromosome 1 and male infertility.

Li R, Fan H, Zhang Q, Yang X, Zhan P, Feng S Open Med (Wars). 2020; 15(1):343-348.

PMID: 33335995 PMC: 7712408. DOI: 10.1515/med-2020-0404.


Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies.

Potter S, Bragg J, Blom M, Deakin J, Kirkpatrick M, Eldridge M Front Genet. 2017; 8:10.

PMID: 28265284 PMC: 5301020. DOI: 10.3389/fgene.2017.00010.


Recombination and synaptic adjustment in oocytes of mice heterozygous for a large paracentric inversion.

Torgasheva A, Rubtsov N, Borodin P Chromosome Res. 2013; 21(1):37-48.

PMID: 23354734 DOI: 10.1007/s10577-012-9336-6.


Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest.

Meschede D, Froster U, Bergmann M, Nieschlag E J Med Genet. 1994; 31(7):573-5.

PMID: 7966196 PMC: 1049983. DOI: 10.1136/jmg.31.7.573.


References
1.
Luciani J, Morazzani M, Stahl A . Identification of pachytene bivalents in human male meiosis using G-banding technique. Chromosoma. 1975; 52(3):275-82. DOI: 10.1007/BF00332116. View

2.
Geraedts J, Pearson P . Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population. Clin Genet. 1974; 6(4):247-57. DOI: 10.1111/j.1399-0004.1974.tb02086.x. View

3.
Oud J, de Jong J, de Rooij D . A sequential analysis of meiosis in the male mouse using a restricted spermatocyte population obtained by a hydroxyurea/triaziquone treatment. Chromosoma. 1979; 71(2):237-48. DOI: 10.1007/BF00292826. View

4.
Luciani J, Guichaoua M, Morazzani M . Complete pachytene chromomere karyotypes of human spermatocyte bivalents. Hum Genet. 1984; 66(2-3):267-71. DOI: 10.1007/BF00286614. View

5.
Van der Linden A, Pearson P, van de Kamp J . Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4. Cytogenet Cell Genet. 1975; 14(2):126-39. DOI: 10.1159/000130332. View