Literature DB >> 3612704

Pericentric inversion in human chromosome 1 and the risk for male sterility.

A C Chandley, S McBeath, R M Speed, L Yorston, T B Hargreave.   

Abstract

A pericentric inversion in chromosome 1 of a severely oligospermic human male is reported. Pachytene analysis in microspread preparations shows an absence of full loop formation in the inversion bivalent and only the rare occurrence of a partial loop. The majority of cells exhibit extensive asynapsis across the inverted segment, or a normal looking synaptonemal complex indicative of heterologous pairing along the length of the inversion. Crossing over is reduced in the No 1 bivalent with only a rare chiasma being seen in the inverted region at metaphase I. Males heterozygous for a pericentric inversion in chromosome 1 appear to be at severe risk for infertility brought about by spermatogenic disturbance. The dearth of full loops at prophase in this patient, and in other pericentric inversion cases studied both in man and other species, raises the question of whether recombinant offspring might be rarer than anticipated on a theoretical basis owing to asynapsis or early heterologous synapsis across inverted segments.

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Year:  1987        PMID: 3612704      PMCID: PMC1050097          DOI: 10.1136/jmg.24.6.325

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  12 in total

1.  AN AIR-DRYING METHOD FOR MEIOTIC PREPARATIONS FROM MAMMALIAN TESTES.

Authors:  E P EVANS; G BRECKON; C E FORD
Journal:  Cytogenetics       Date:  1964

2.  Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers.

Authors:  G R Sutherland; A J Gardiner; R F Carter
Journal:  Clin Genet       Date:  1976-07       Impact factor: 4.438

3.  Loop formation and synaptic adjustment in a human male heterozygous for two pericentric inversions.

Authors:  M R Guichaoua; D Delafontaine; R Taurelle; J L Taillemite; M R Morazzani; J M Luciani
Journal:  Chromosoma       Date:  1986       Impact factor: 4.316

4.  Centromere staining at meiosis in man.

Authors:  A C Chandley; J M Fletcher
Journal:  Humangenetik       Date:  1973-05-25

5.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

6.  Familial inv(1) (p3500q21.3) associated with azoospermia.

Authors:  H Rivera; M C Alvarez-Arratia; M Moller; M Díaz; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 7.  Sex-chromosome pairing and male fertility.

Authors:  G L Miklos
Journal:  Cytogenet Cell Genet       Date:  1974

8.  Pericentric inversion of chromosome 1 in three sterile brothers.

Authors:  A Giraldo; E Silva; I Martínez; C Campos; J Guzmán
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Pericentric inversion of chromosome 1 in an azoospermic man.

Authors:  A Tóth; M Gaál; G Sára; J László
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

10.  On the nature and extent of XY pairing at meiotic prophase in man.

Authors:  A C Chandley; P Goetz; T B Hargreave; A M Joseph; R M Speed
Journal:  Cytogenet Cell Genet       Date:  1984
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  20 in total

1.  Chromosomal alterations and male infertility.

Authors:  A Antonelli; L Gandini; P Petrinelli; L Marcucci; R Elli; F Lombardo; F Dondero; A Lenzi
Journal:  J Endocrinol Invest       Date:  2000-11       Impact factor: 4.256

2.  Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse.

Authors:  P M Borodin; I P Gorlov
Journal:  Chromosoma       Date:  1990-09       Impact factor: 4.316

3.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

4.  Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation.

Authors:  M R Guichaoua; B Quack; R M Speed; B Noel; A C Chandley; J M Luciani
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

5.  The extent, mechanism, and consequences of genetic variation, for recombination rate.

Authors:  W P Robinson
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

6.  Male infertility associated with de novo pericentric inversion of chromosome 1.

Authors:  Özgür Balasar; Ayşe Gül Zamani; Mehmet Balasar; Hasan Acar
Journal:  Turk J Urol       Date:  2017-12-01

7.  Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion.

Authors:  A de Perdigo; O Gabriel-Robez; Y Rumpler
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

8.  Heterosynapsis in a heterozygous fertile boar carrier of a 3;7 translocation.

Authors:  O Gabriel-Robez; H Jaafar; C Ratomponirina; J Boscher; J Bonneau; C P Popescu; Y Rumpler
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

9.  Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs).

Authors:  A C Chandley; J R Gosden; T B Hargreave; G Spowart; R M Speed; S McBeath
Journal:  J Med Genet       Date:  1989-03       Impact factor: 6.318

10.  Prophase of meiosis in human spermatocytes analysed by EM microspreading in infertile men and their controls and comparisons with human oocytes.

Authors:  R M Speed; A C Chandley
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

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