Literature DB >> 3319437

Two different XY-quadrivalent associations and impairment of fertility in men.

R Johannisson1, U Löhrs, H H Wolff, E Schwinger.   

Abstract

One sterile and one subfertile man with balanced reciprocal autosomal translocations, a t(9;15), and a t(14;21), were analyzed using whole mount pachytene spreads, histology, and semen analyses. In both probands with different types of quadrivalent complexes lack of pairing near the translocation breakpoints and significant associations with XY bivalents were found. Variability in the frequency of XY-quadrivalent contacts and an increase in late pachytene to 52% in t(9;15) and 90% in t(14;21) could be observed. The lower rate was associated with reduced postmeiotic spermatogenesis and the higher rate with complete spermatogenic arrest. In both translocation carriers the XY-quadrivalent association is considered to be the main cause for testicular malfunction rather than nonpaired segments in the multivalent complexes.

Entities:  

Mesh:

Year:  1987        PMID: 3319437     DOI: 10.1159/000132458

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  17 in total

1.  Bivalent 15 regularly associates with the sex vesicle in normal male meiosis.

Authors:  C Metzler-Guillemain; C Mignon; D Depetris; M R Guichaoua; M G Mattei
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13).

Authors:  A S Goldman; R H Martin; R Johannisson; C P Gould; E V Davison; J E Emslie; J Burn; M A Hultén
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

3.  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

4.  Three dimensional reconstruction of human pachytene spermatocyte nuclei of a 17;21 reciprocal translocation carrier: study of XY-autosome relationships.

Authors:  M R Guichaoua; A de Lanversin; C Cataldo; D Delafontaine; C Alasia; M Fraterno; P Terriou; A Stahl; J M Luciani
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

5.  Pattern of ribonucleic acid synthesis in vitro in primary spermatocytes from mouse testis carrying an X-autosome translocation.

Authors:  H Jaafar; O Gabriel-Robez; Y Rumpler
Journal:  Chromosoma       Date:  1989-11       Impact factor: 4.316

6.  Spermatogenesis in two patients with the fragile X syndrome. II. First meiosis: light and electron microscopy.

Authors:  R Johannisson; U Froster-Iskenius; N Saadallah; M A Hultén
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

7.  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

8.  Synaptonemal complexes of chains and rings in mice heterozygous for multiple Robertsonian translocations.

Authors:  R Johannisson; H Winking
Journal:  Chromosome Res       Date:  1994-03       Impact factor: 5.239

9.  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

10.  Deficiency of X and Y chromosomal pairing at meiotic prophase in spermatocytes of sterile interspecific hybrids between laboratory mice (Mus domesticus) and Mus spretus.

Authors:  Y Matsuda; P B Moens; V M Chapman
Journal:  Chromosoma       Date:  1992-06       Impact factor: 4.316

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