Literature DB >> 6500577

Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype.

D A Laurie, R W Palmer, M A Hultén.   

Abstract

The frequency and distribution of chiasmata was investigated in two fertile carriers of reciprocal translocations, one with a 46,XY,t(9;10)(p22;q24) karyotype and one with a 46,X,-Y,+der(Y),t(Y;10)(q12;q24) karyotype. In both cases the chromosomes involved in the translocation showed an increase in chiasma frequency in comparison to karyotypically normal controls and in both cases this increase was localised, affecting only one interstitial segment of each translocation quadrivalent. In the t(9;10) case chiasmata appeared in substantial numbers in a novel location, the proximal two thirds of 9p, while in the t(Y;10) case chiasmata appeared in a conventional location, the medial region of 10q, but at an increased frequency. Furthermore there was evidence for inter-chromosomal effects in the t(9;10) case.

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Year:  1984        PMID: 6500577     DOI: 10.1007/bf00418394

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  31 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.  Comparative chiasma analysis using a computerised optical digitiser.

Authors:  D D Shaw; G R Knowles
Journal:  Chromosoma       Date:  1976-12-16       Impact factor: 4.316

Review 3.  The chromosomal basis of human infertility.

Authors:  A C Chandley
Journal:  Br Med Bull       Date:  1979-05       Impact factor: 4.291

Review 4.  Cytogenetic aspects of human male meiosis.

Authors:  M Hultén; J Lindsten
Journal:  Adv Hum Genet       Date:  1973

5.  Developmental variation of chiasma frequency in Chorthippus brunneus.

Authors:  I Maudlin
Journal:  Heredity (Edinb)       Date:  1972-10       Impact factor: 3.821

6.  Chiasma-derived genetic lengths and recombination fractions: a reciprocal translocation 46,XY,t(1;22) (q32;q13).

Authors:  R W Palmer; M A Hultén
Journal:  Ann Hum Genet       Date:  1983-10       Impact factor: 1.670

7.  Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2, and 9.

Authors:  D A Laurie; M Hultén; G H Jones
Journal:  Cytogenet Cell Genet       Date:  1981

8.  Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male.

Authors:  P Petit; A Unglik; J P Fryns
Journal:  Ann Genet       Date:  1982

9.  Synthesis and properties of a double translocation heterozygote involving a stable ring-of-six interchange in the German cockroach.

Authors:  M H Ross; D G Cochran
Journal:  J Hered       Date:  1981 Jan-Feb       Impact factor: 2.645

Review 10.  The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

Authors:  E Lifschytz; D L Lindsley
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

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  15 in total

1.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

2.  A t(Y;15) translocation with a deletion of the proximal Yq in a boy with mixed gonadal dysgenesis.

Authors:  M Shinohara; S Minowada; Y Aso; K Yamada; Y Nakahori; T Tamura; Y Nakagome
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

3.  Human sperm chromosome studies in a reciprocal translocation t(2;5).

Authors:  C Templado; J Navarro; J Benet; A Genescà; M M Pérez; J Egozcue
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

4.  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

5.  Partial trisomy 13q resulting from a paternal reciprocal Yq;13q translocation.

Authors:  J Nikolis; K Ivanović; V Diklić
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

6.  Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Authors:  G M Brown; M Leversha; M Hulten; M A Ferguson-Smith; N A Affara; R A Furlong
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

7.  Altered bivalent positioning in metaphase I human spermatocytes from Robertsonian translocation carriers.

Authors:  Mireia Solé; Joan Blanco; Oliver Valero; Laia Vergés; Francesca Vidal; Zaida Sarrate
Journal:  J Assist Reprod Genet       Date:  2016-09-21       Impact factor: 3.412

Review 8.  The genetics of human reproduction.

Authors:  A C Chandley
Journal:  Experientia       Date:  1986-10-15

9.  Chiasma-based genetic map of the mouse X chromosome.

Authors:  M A Hultén; C Tease; N M Lawrie
Journal:  Chromosoma       Date:  1995-11       Impact factor: 4.316

10.  Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: quadrivalent configuration, orientation and first meiotic segregation.

Authors:  A S Goldman; M A Hultén
Journal:  Chromosoma       Date:  1993-01       Impact factor: 4.316

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