Literature DB >> 3737403

Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences.

N A Affara, L Florentin, N Morrison, K Kwok, M Mitchell, A Cook, D Jamieson, L Glasgow, L Meredith, E Boyd.   

Abstract

A series of Y recombinants have been isolated from Y-specific DNA libraries and regionally located on the Y chromosome using a Y deletion panel constructed from individuals carrying structural abnormalities of the Y chromosome. Of twenty recombinants examined twelve have been assigned to Yp and eight to Yq. Five of the Yp recombinants map between Yp11.2 and Ypter and one can only be assigned to Yp. Of the former, four detect homologies on the X chromosome between Xq13 and Xq24 and the latter one between Xp22.3 and Xpter. The sixth recombinant detects autosomal homologous sequences. The six remaining Yp probes are located between Ycen and Yp11.2. One of these detects a homology on the X chromosome at Xq13-Xq24 and a series of autosomal sequences, two detect uniquely Y-specific sequences and three a complex pattern of autosomal homologies. The remaining eight recombinants have been assigned to three intervals on Yq. Of three recombinants located between Ycen and Yq11.21 two detect only Y sequences and one additional autosomal homologies. Two recombinants lie in the interval Yq11.21-Yq11-22, one of which detects only Y sequences and the other an Xp homology between Xp22.3 and Xpter. Finally, the three remaining Yq recombinants all detect autosomal homologies and are located between Yq11.22 and Yq12. The divergence between homologies on different chromosomes has been examined for three recombinants by washing Southern Blots at different levels of stringency. Additionally, Southern analysis of DNA from flow sorted chromosomes has been used to identify autosomes carrying homologies to two of the Y recombinants.

Mesh:

Year:  1986        PMID: 3737403      PMCID: PMC311545          DOI: 10.1093/nar/14.13.5353

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  32 in total

1.  Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal.

Authors:  H J Cooke; W R Brown; G A Rappold
Journal:  Nature       Date:  1985 Oct 24-30       Impact factor: 49.962

2.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

3.  Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.

Authors:  G M Wahl; M Stern; G R Stark
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

4.  X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome.

Authors:  M A Ferguson-Smith
Journal:  Lancet       Date:  1966-08-27       Impact factor: 79.321

5.  Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.

Authors:  D Page; B de Martinville; D Barker; A Wyman; R White; U Francke; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

6.  Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.

Authors:  L M Kunkel; U Tantravahi; M Eisenhard; S A Latt
Journal:  Nucleic Acids Res       Date:  1982-03-11       Impact factor: 16.971

7.  High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry.

Authors:  B D Young; M A Ferguson-Smith; R Sillar; E Boyd
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

8.  Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase.

Authors:  S P Daiger; R S Wildin; T S Su
Journal:  Nature       Date:  1982-08-12       Impact factor: 49.962

9.  Pairing of X and Y chromosomes, non-inactivation of X-linked genes, and the maleness factor.

Authors:  P E Polani
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 10.  Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Authors:  R M Davis
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

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  17 in total

1.  Deletion mapping of interval 6 of the human Y chromosome.

Authors:  M Kotecki; J Jaruzelska; M Skowrońska; P Fichna
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

2.  Deletion mapping of 39 random isolated Y-chromosome DNA fragments.

Authors:  C J Oosthuizen; J S Herbert; L K Vermaak; J Brusnicky; J Fricke; L du Plessis; A E Retief
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

3.  Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9.

Authors:  N A Affara; D Chambers; J O'Brien; S S Habeebu; M Kalaitsidaki; C E Bishop; M A Ferguson-Smith
Journal:  Nucleic Acids Res       Date:  1989-04-25       Impact factor: 16.971

4.  Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment.

Authors:  W A Bickmore; H J Cooke
Journal:  Nucleic Acids Res       Date:  1987-08-11       Impact factor: 16.971

5.  Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.

Authors:  N A Affara; M A Ferguson-Smith; R E Magenis; J L Tolmie; E Boyd; A Cooke; D Jamieson; K Kwok; M Mitchell; L Snadden
Journal:  Nucleic Acids Res       Date:  1987-09-25       Impact factor: 16.971

6.  Isolation of a sequence which maps close to the human sex determining gene.

Authors:  C A Pritchard; P J Goodfellow; P N Goodfellow
Journal:  Nucleic Acids Res       Date:  1987-08-11       Impact factor: 16.971

7.  An X-linked zinc finger gene mapping to Xq21.1-q21.3 closely related to ZFX and ZFY: possible origins from a common ancestral gene.

Authors:  S L Lloyd; C A Sargent; J Chalmers; E Lim; S S Habeebu; N A Affara
Journal:  Nucleic Acids Res       Date:  1991-09-25       Impact factor: 16.971

8.  X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.

Authors:  P H Yen; S P Tsai; S L Wenger; M W Steele; T K Mohandas; L J Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-15       Impact factor: 11.205

9.  A human Y-chromosomal DNA sequence expressed in testicular tissue.

Authors:  J Arnemann; J T Epplen; H J Cooke; U Sauermann; W Engel; J Schmidtke
Journal:  Nucleic Acids Res       Date:  1987-11-11       Impact factor: 16.971

10.  A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.

Authors:  K McElreavey; E Vilain; N Abbas; I Herskowitz; M Fellous
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

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