Literature DB >> 2501212

Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region.

B Arveiler1, A Vincent, J L Mandel.   

Abstract

We are using pulsed-field gel electrophoresis (PFGE) to establish a physical map of the human Xq28 region. We have identified a new probe 35.239 (DXYS64), localized in Xq28 by somatic hybrid mapping and belonging to a region of greater than 99% homology between the X and the Y chromosomes. PFGE data show that probes 35.239 and the polymorphic locus DXS115 (probe 767) map within a common 300-kb BssHII fragment. Both probes, in addition, hybridize to 575-kb BssHII and 590-kb ClaI fragments that contain the gene coding for coagulation factor VIII (F8C). The order F8C-DXS115-DXYS64 could be determined. Our results also provide evidence for linkage between the red/green color vision locus (RCP,GCP) and probes MD13 and T1.7 (GdX, DXS254) within a 750-kb ClaI fragment. Although the latter two probes are located within 50 kb of the 3' end of the G6PD gene, a G6PD cDNA probe did not hybridize to this fragment. G6PD, on the other hand, could be linked to F8C on a 290-kb BssHII fragment. All these data allow us to propose the order (RCP,GCP)-MD13-GdX-G6PD-F8C-DXS115-DXYS 64. We also linked probes St14 (DXS52), MN12 (DXS33), and DX13 (DXS15) to a member of a small family of X-linked dispersed sequences (DNF22S3) within a 575-kb BssHII fragment. The preliminary physical map presented here should be useful for further fine mapping of disease genes in the Xq28 region and should be helpful in orientating efforts toward the cloning of sequences close to the fragile X syndrome.

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Year:  1989        PMID: 2501212     DOI: 10.1016/0888-7543(89)90269-3

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  20 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

Authors:  M J Higgins; C Turmel; J Noolandi; P E Neumann; M Lalande
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

Review 4.  The fragile X: progress toward solving the puzzle.

Authors:  W T Brown
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

5.  Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Authors:  R Feil; G Palmieri; M d'Urso; R Heilig; I Oberlé; J L Mandel
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

6.  Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.

Authors:  M V Bell; J Bloomfield; M McKinley; M N Patterson; M G Darlison; E A Barnard; K E Davies
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

7.  A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Authors:  A Vincent; C Kretz; I Oberlé; J L Mandel
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

8.  Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis.

Authors:  M M Khalifa; A L Reiss; B R Migeon
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

9.  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

10.  Physical map of human Xq27-qter: localizing the region of the fragile X mutation.

Authors:  A Poustka; A Dietrich; G Langenstein; D Toniolo; S T Warren; H Lehrach
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

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