Literature DB >> 8110480

Construction and characterization of partial digest DNA libraries made from flow-sorted human chromosome 16.

J L Longmire1, N C Brown, L J Meincke, M L Campbell, K L Albright, J J Fawcett, E W Campbell, R K Moyzis, C E Hildebrand, G A Evans.   

Abstract

In this report, we present the techniques used for the construction of chromosome-specific partial digest libraries from flow-sorted chromosomes and the characterization of two such libraries from human chromosome 16. These libraries were constructed to provide materials for use in the development of a high-resolution physical map of human chromosome 16, and as part of a distributive effort on the National Laboratory Gene Library Project. Libraries with 20-fold coverage were made in Charon-40 (LA16NL03) and in sCos-1 (LA16NC02) after chromosome 16 was sorted from a mouse-human monochromosomal hybrid cell line containing a single homologue of human chromosome 16. Both libraries are approximately 90% enriched for human chromosome 16, have low nonrecombinant backgrounds, and are highly representative for human chromosome-16 sequences. The cosmid library in particular has provided a valuable resource for the isolation of coding sequences, and in the ongoing development of a physical map of human chromosome 16.

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Year:  1993        PMID: 8110480     DOI: 10.1016/1050-3862(93)90037-j

Source DB:  PubMed          Journal:  Genet Anal Tech Appl        ISSN: 1050-3862


  8 in total

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Authors:  Anthony W I Lo; Laure Sabatier; Bijan Fouladi; Géraldine Pottier; Michelle Ricoul; John P Murnane
Journal:  Neoplasia       Date:  2002 Nov-Dec       Impact factor: 5.715

2.  Molecular characterization of patients with 18q23 deletions.

Authors:  G Strathdee; R Sutherland; J J Jonsson; R Sataloff; M Kohonen-Corish; D Grady; J Overhauser
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

3.  Selection of a sublibrary enriched for a chromosome from total human bacterial artificial chromosome library using DNA from flow sorted chromosomes as hybridization probes.

Authors:  U J Kim; H Shizuya; L Deaven; X N Chen; J R Korenberg; M I Simon
Journal:  Nucleic Acids Res       Date:  1995-05-25       Impact factor: 16.971

4.  Characterization of a cosmid library from flow-sorted chromosomes 11.

Authors:  B H Weber; H Stöhr; I Siedlaczck; J L Longmire; L L Deaven; A M Duncan; O Riess
Journal:  Chromosome Res       Date:  1994-05       Impact factor: 5.239

5.  TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.

Authors:  C A Wise; L C Chiang; W A Paznekas; M Sharma; M M Musy; J A Ashley; M Lovett; E W Jabs
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

6.  Human Rad50 is physically associated with human Mre11: identification of a conserved multiprotein complex implicated in recombinational DNA repair.

Authors:  G M Dolganov; R S Maser; A Novikov; L Tosto; S Chong; D A Bressan; J H Petrini
Journal:  Mol Cell Biol       Date:  1996-09       Impact factor: 4.272

7.  How bats achieve a small C-value: frequency of repetitive DNA in Macrotus.

Authors:  R A Van den Bussche; J L Longmire; R J Baker
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

8.  Increased sensitivity of subtelomeric regions to DNA double-strand breaks in a human cancer cell line.

Authors:  Oliver Zschenker; Avanti Kulkarni; Douglas Miller; Gloria E Reynolds; Marine Granger-Locatelli; Géraldine Pottier; Laure Sabatier; John P Murnane
Journal:  DNA Repair (Amst)       Date:  2009-06-18
  8 in total

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