Literature DB >> 4073835

Meiotic chromosome pairing in the normal human female.

B M Wallace, M A Hultén.   

Abstract

The synaptonemal complexes of oocytes from 16-22 week human fetuses were spread using detergent and silver-stained for examination by light microscopy. Zygotene chromosome synapsis generally begins at the telomeres, without obvious prealignment, and proceeds towards the centromeres. Synapsis is not synchronous and longer bivalents may sometimes be completely paired before shorter ones. At pachytene, when pairing is usually complete, some regions presumed to correspond to the heterochromatic blocks of chromosomes 1.9 and 16 may remain unpaired. Residual univalents are uncommon, and little interlocking is evident at this stage. Desynapsis indicating the beginning of diplotene frequently begins at the telomeres, although there is a general relaxation of pairing throughout the bivalents which become increasingly diffuse as diplotene proceeds. The total synaptonemal complex complement length at pachytene in the female is 519 micron, which is about twice that found in the human male. The implications of these results for genetic mapping are discussed.

Entities:  

Mesh:

Year:  1985        PMID: 4073835     DOI: 10.1111/j.1469-1809.1985.tb01695.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  22 in total

1.  A sequence-based integrated map of chromosome 22.

Authors:  W J Tapper; N E Morton; I Dunham; X Ke; A Collins
Journal:  Genome Res       Date:  2001-07       Impact factor: 9.043

2.  Patterns of meiotic recombination in human fetal oocytes.

Authors:  Charles Tease; Geraldine M Hartshorne; Maj A Hultén
Journal:  Am J Hum Genet       Date:  2002-05-01       Impact factor: 11.025

3.  Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male.

Authors:  Petrice W Brown; Luann Judis; E Ricky Chan; Stuart Schwartz; Allen Seftel; Anthony Thomas; Terry J Hassold
Journal:  Am J Hum Genet       Date:  2005-08-16       Impact factor: 11.025

4.  XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

Authors:  T J Hassold; S L Sherman; D Pettay; D C Page; P A Jacobs
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

5.  The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Authors:  G Floridia; M Piantanida; A Minelli; C Dellavecchia; C Bonaglia; E Rossi; G Gimelli; G Croci; F Franchi; S Gilgenkrantz; P Grammatico; L Dalprá; S Wood; C Danesino; O Zuffardi
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

6.  Analysis of meiotic chromosome pairing in the female mouse using a novel minichromosome.

Authors:  C Tease; G Fisher
Journal:  Chromosome Res       Date:  1998-06       Impact factor: 5.239

7.  The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

8.  Sequential study of the synaptonemal complex in rat (Rattus norvegicus) oocytes by light and electron microscopy.

Authors:  R Pujol; M Garcia; L Freixa; J Egozcue
Journal:  Genetica       Date:  1988-11-30       Impact factor: 1.082

9.  Development of the first meiotic prophase stages in human fetal oocytes observed by light and electron microscopy.

Authors:  M Garcia; A J Dietrich; L Freixa; A C Vink; M Ponsà; J Egozcue
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

10.  High-resolution crossover maps for each bivalent of Zea mays using recombination nodules.

Authors:  Lorinda K Anderson; Gregory G Doyle; Brian Brigham; Jenna Carter; Kristina D Hooker; Ann Lai; Mindy Rice; Stephen M Stack
Journal:  Genetics       Date:  2003-10       Impact factor: 4.562

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.