Literature DB >> 6620330

Chiasma distribution, genetic lengths, and recombination fractions: a comparison between chromosomes 15 and 16.

N Saadallah, M Hultén.   

Abstract

The chiasma distribution of bivalents 15 and 16 identified at diakinesis by a quadruple staining technique including DA-DAPI fluorescence has been investigated in two human males. The study has shown that chiasmata are not distributed at random. Both chromosomes have distally localised chiasmata, but in the long arm of chromosome 15 chiasmata are also found to be localised proximally, adjacent to the centromere. Genetic lengths and recombination fractions have been calculated from chiasma distribution data for the major bands of chromosomes 15 and 16 under the assumptions that there is no chromatid interference, no chiasma movement, and no difference between mitotic and meiotic band positions. The localisation of chiasmata implies much discrepancy in recombination patterns between the acrocentric chromosome 15 and the submetacentric chromosome 16.

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Mesh:

Year:  1983        PMID: 6620330      PMCID: PMC1049122          DOI: 10.1136/jmg.20.4.290

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


  10 in total

1.  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 2.  Cytogenetic aspects of human male meiosis.

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

3.  Chiasma distribution at diakinesis in the normal human male.

Authors:  M Hultén
Journal:  Hereditas       Date:  1974       Impact factor: 3.271

4.  Chiasma derived genetic maps and recombination fractions: chromosome 1.

Authors:  M A Hultén; R W Palmer; D A Laurie
Journal:  Ann Hum Genet       Date:  1982-05       Impact factor: 1.670

5.  Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

Authors:  D Schweizer; P Ambros; M Andrle
Journal:  Exp Cell Res       Date:  1978-02       Impact factor: 3.905

6.  Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis.

Authors:  T Caspersson; M Hultén; J Lindsten; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

7.  Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes.

Authors:  U Francke; N Oliver
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

8.  Chiasma derived genetic lengths and recombination fractions: chromosomes 2 and 9.

Authors:  D A Laurie; R W Palmer; M A Hultén
Journal:  Ann Hum Genet       Date:  1982-07       Impact factor: 1.670

9.  Analysis of crossing over in mouse meiotic cells by BrdU labelling technique.

Authors:  N Kanda; H Kato
Journal:  Chromosoma       Date:  1980       Impact factor: 4.316

Review 10.  A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies.

Authors:  F H Ruddle
Journal:  Nature       Date:  1981-11-12       Impact factor: 49.962

  10 in total
  17 in total

1.  Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.

Authors:  D R Higgs; J S Wainscoat; J Flint; A V Hill; S L Thein; R D Nicholls; H Teal; H Ayyub; T E Peto; A G Falusi
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

2.  The association of Angelman's syndrome with deletions within 15q11-13.

Authors:  M Pembrey; S J Fennell; J van den Berghe; M Fitchett; D Summers; L Butler; C Clarke; M Griffiths; E Thompson; M Super
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 3.  The role of somatic cell genetics in human gene mapping.

Authors:  K H Grzeschik
Journal:  Experientia       Date:  1986-10-15

4.  Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.

Authors:  P Harris; M Lalande; H Stroh; G Bruns; A Flint; S A Latt
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

5.  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

6.  Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors:  A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

7.  Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Authors:  S L Christian; W P Robinson; B Huang; A Mutirangura; M R Line; M Nakao; U Surti; A Chakravarti; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

Review 8.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination.

Authors:  W P Robinson; R Spiegel; A A Schinzel
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

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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