Literature DB >> 2945430

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene.

J J Wasmuth, L R Carlock, B Smith, L L Immken.   

Abstract

Somatic cell hybrids were selected that retain a derivative chromosome 5 from an individual in which the p15.1-pter segment of chromosome 5 is replaced with the p15.1-pter segment of chromosome 4. Hybrids that retain this derivative chromosome exclusively were found to be positive for G8, a DNA marker closely linked to the Huntington disease gene on chromosome 4p. From one such hybrid, a segregant was isolated that had deleted the entire q arm of the derivative chromosome but retained the p arm intact as its only detectable human DNA. A complete recombinant DNA library was prepared from this cell line, and the inserts in approximately 1/3 of the recombinant phage with human DNA were shown to be derived from 4pter-4p15.1, which represents only approximately 1% of the total human genome. The cell hybrid and DNA library represent a rapid and efficient means to identify and isolate many polymorphic DNA markers close to and flanking the Huntington disease gene.

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Year:  1986        PMID: 2945430      PMCID: PMC1683957     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  14 in total

1.  In vitro packaging of lambda and cosmid DNA.

Authors:  B Hohn
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

2.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

3.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

4.  A polymorphic DNA marker genetically linked to Huntington's disease.

Authors:  J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal:  Nature       Date:  1983 Nov 17-23       Impact factor: 49.962

5.  Lambda replacement vectors carrying polylinker sequences.

Authors:  A M Frischauf; H Lehrach; A Poustka; N Murray
Journal:  J Mol Biol       Date:  1983-11-15       Impact factor: 5.469

6.  Removal of repeated sequences from hybridisation probes.

Authors:  P G Sealey; P A Whittaker; E M Southern
Journal:  Nucleic Acids Res       Date:  1985-03-25       Impact factor: 16.971

7.  Linkage of the leuS, emtB, and chr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human--Chinese hamster hybrids.

Authors:  S Dana; J J Wasmuth
Journal:  Somatic Cell Genet       Date:  1982-03

8.  Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.

Authors:  L R Carlock; J J Wasmuth
Journal:  Somat Cell Mol Genet       Date:  1985-05

9.  Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.

Authors:  S Dana; J J Wasmuth
Journal:  Mol Cell Biol       Date:  1982-10       Impact factor: 4.272

10.  Propagation of some human DNA sequences in bacteriophage lambda vectors requires mutant Escherichia coli hosts.

Authors:  A R Wyman; L B Wolfe; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

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  19 in total

1.  Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Authors:  H S Stadler; B J Padanilam; K Buetow; J C Murray; M Solursh
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

2.  Structural and transcriptional analysis of a human subtelomeric repeat.

Authors:  J F Cheng; C L Smith; C R Cantor
Journal:  Nucleic Acids Res       Date:  1991-01-11       Impact factor: 16.971

Review 3.  Long-range walking techniques in positional cloning strategies.

Authors:  L Stubbs
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

4.  Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.

Authors:  J E Richards; T C Gilliam; J L Cole; M L Drumm; J J Wasmuth; J F Gusella; F S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

5.  Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.

Authors:  B Smith; D Skarecky; U Bengtsson; R E Magenis; N Carpenter; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

6.  Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.

Authors:  W L Whaley; F Michiels; M E MacDonald; D Romano; M Zimmer; B Smith; J Leavitt; M Bucan; J L Haines; T C Gilliam
Journal:  Nucleic Acids Res       Date:  1988-12-23       Impact factor: 16.971

7.  A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.

Authors:  M R Hayden; J Hewitt; J J Wasmuth; J J Kastelein; S Langlois; M Conneally; J Haines; B Smith; C Hilbert; D Allard
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

8.  Isolation of polymorphic DNA fragments from human chromosome 4.

Authors:  T C Gilliam; S T Healey; M E MacDonald; G D Stewart; J J Wasmuth; R E Tanzi; J C Roy; J F Gusella
Journal:  Nucleic Acids Res       Date:  1987-02-25       Impact factor: 16.971

9.  The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere.

Authors:  N A Doggett; J F Cheng; C L Smith; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

10.  A recombination event that redefines the Huntington disease region.

Authors:  R G Snell; L M Thompson; D A Tagle; T L Holloway; G Barnes; H G Harley; L A Sandkuijl; M E MacDonald; F S Collins; J F Gusella
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

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