Literature DB >> 6087473

Isolation and characterization of human random cDNA clones homologous to DNA from the X chromosome.

I Balazs, M Purrello, D M Kurnit, K H Grzeschik, M Siniscalco.   

Abstract

To search for human X-chromosome-specific probes useful for molecular mapping, we studied recombinant clones isolated from a human cDNA library. DNA preparations from 150 randomly selected clones were labeled and annealed to XY and 4XY human DNA, and to DNA from a human-mouse hybrid cell line that had retained only the human X-chromosome (A9/HRBC2). cDNA clones sharing homology with DNA from the X chromosome annealed to A9/HRBC2-DNA and hybridized more intensely to 4XY DNA than to XY DNA. Eleven such clones were identified. Of these, three hybridized only to X chromosomal DNA while the rest also annealed to DNA from one or more autosomes. Chromosomal assignment of the autosomal DNA fragments showed that, in addition to hybridization to X chromosomal DNA, four of the clones hybridized to DNA sequences from chromosome 2 and two clones to chromosome 7. Subregional mapping of the relevant X chromosomal DNA fragments indicated that one clone is homologous to DNA sequences located at Xp21-Xp22, whereas the others are located in the telomeric region of the long arm. The cDNA clones were used to search for restriction fragment length polymorphisms. Several restriction-site polymorphisms were detected. Some corresponded to variants of X chromosomal DNA sequences while others were from autosomes such as chromosomes 2 and 7.

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Year:  1984        PMID: 6087473     DOI: 10.1007/bf01535634

Source DB:  PubMed          Journal:  Somat Cell Mol Genet        ISSN: 0740-7750


  14 in total

1.  The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization.

Authors:  P Krajci; K H Grzeschik; A H Geurts van Kessel; B Olaisen; P Brandtzaeg
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

2.  A novel human multi-locus DNA family detected by pJU78 (DF31).

Authors:  F Peinemann; D N Cooper; K H Grzeschik; J Schmidtke
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

3.  Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors:  M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

4.  Isolation and subregional mapping of an arbitrary cloned probe detecting a common RFLP on human chromosome 2.

Authors:  G N Davatelis
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

5.  Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.

Authors:  I Oberlé; G Camerino; C Kloepfer; J P Moisan; K H Grzeschik; B Hellkuhl; M C Hors-Cayla; N Van Cong; D Weil; J L Mandel
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

6.  Cloning of a cDNA encoding the human cation-dependent mannose 6-phosphate-specific receptor.

Authors:  R Pohlmann; G Nagel; B Schmidt; M Stein; G Lorkowski; C Krentler; J Cully; H E Meyer; K H Grzeschik; G Mersmann
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

7.  Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).

Authors:  J A Nicklas; T C Hunter; J P O'Neill; R J Albertini
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

8.  Isolation and subregional mapping of a human cDNA clone detecting a common RFLP on chromosome 12.

Authors:  I Balazs; M Purrello; B Alhadeff; K H Grzeschik; P Szabo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Individual exons encode the integral membrane domains of human myelin proteolipid protein.

Authors:  H J Diehl; M Schaich; R M Budzinski; W Stoffel
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

10.  Aberrant recombination events in B cell lines derived from a kappa-deficient human.

Authors:  J Stavnezer; O Kekish; D Batter; J Grenier; I Balazs; E Henderson; B J Zegers
Journal:  Nucleic Acids Res       Date:  1985-05-24       Impact factor: 16.971

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