Literature DB >> 3180846

Meiotic analysis of two human reciprocal X-autosome translocations.

B Quack1, R M Speed, J M Luciani, B Noel, M Guichaoua, A C Chandley.   

Abstract

Two cases of human reciprocal X-autosome translocation, t(X;12) and t(X;2), are described in sterile males, along with meiotic findings. Each carrier had inherited the translocation from his mother. Both showed azoospermia and germ-cell maturation arrest at the primary spermatocyte level, with most cells being arrested at the pachytene stage. A few metaphase I (MI) divisions were found, with occasional metaphase II cells being seen in the t(X;2) carrier. MI air-dried preparations gave clear evidence of chain quadrivalent formation. In the t(X;2) heterozygote, the pairing characteristics of the quadrivalent at pachytene were also analyzed in electron microscopic spreads. Disturbance of pairing around the breakpoints characterized most quadrivalents, and there was evidence in about 20% of the cells that nonhomologous pairing had taken place between the translocated chromosomes and the normal chromosome 2. Comparisons are made with similar nonhomologous pairing configurations seen at pachytene in quadrivalents of male reciprocal X-autosome translocations of the mouse.

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Year:  1988        PMID: 3180846     DOI: 10.1159/000132583

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


  10 in total

1.  Viability of X-autosome translocations in mammals: an epigenomic hypothesis from a rodent case-study.

Authors:  G Dobigny; C Ozouf-Costaz; C Bonillo; V Volobouev
Journal:  Chromosoma       Date:  2004-07-09       Impact factor: 4.316

Review 2.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Authors:  S E Bodrug; J R Roberson; L Weiss; P N Ray; R G Worton; D L Van Dyke
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

4.  Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions.

Authors:  Carolina J Jorgez; John W Weedin; Aysegul Sahin; Mounia Tannour-Louet; Shuo Han; Juan C Bournat; Anna Mielnik; Sau Wai Cheung; Ajay K Nangia; Peter N Schlegel; Larry I Lipshultz; Dolores J Lamb
Journal:  J Clin Endocrinol Metab       Date:  2011-01-20       Impact factor: 5.958

5.  Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.

Authors:  Yuhua Huang; Ruhui Tian; Junwei Xu; Zhiyong Ji; Yuxiang Zhang; Liangyu Zhao; Chao Yang; Peng Li; Erlei Zhi; Haowei Bai; Sha Han; Jiaqiang Luo; Jingpeng Zhao; Jing Zhang; Zhi Zhou; Zheng Li; Chencheng Yao
Journal:  BMC Med Genomics       Date:  2022-06-19       Impact factor: 3.622

6.  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

7.  Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.

Authors:  J P Giacalone; U Francke
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

8.  Mutational analysis of the human FATE gene in 144 infertile men.

Authors:  Christian Olesen; Joachim Silber; Hans Eiberg; Erik Ernst; Karsten Petersen; Svend Lindenberg; Niels Tommerup
Journal:  Hum Genet       Date:  2003-06-14       Impact factor: 4.132

9.  Molecular and cytogenetic characterization of two azoospermic patients with X-autosome translocation.

Authors:  Suman Lee; Sook-Hwan Lee; Tae-Gyu Chung; Hyun-Joo Kim; Tae-Ki Yoon; In-Pyung Kwak; Sang-Hee Park; Won-Tae Cha; Sung-Won Cho; Kwang-Yul Cha
Journal:  J Assist Reprod Genet       Date:  2003-09       Impact factor: 3.412

10.  Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.

Authors:  S E Bodrug; J J Holden; P N Ray; R G Worton
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

  10 in total

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