Literature DB >> 2068096

Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.

D L Nelson1, A Ballabio, M F Victoria, M Pieretti, R D Bies, R A Gibbs, J A Maley, A C Chinault, T D Webster, C T Caskey.   

Abstract

Over 400 yeast artificial chromosome (YAC) clones were isolated from the human X chromosome, and 110 of these were assigned to regions defined by chromosome translocation and deletion breakpoints. Polymerase chain reaction using Alu primers was applied to YAC clones in order to generate probes, to identify overlapping clones, and to derive "fingerprints" and sequence data directly from total yeast DNA. Several clones were identified in regions of medical interest. One set of three overlapping clones was found to cross a chromosomal translocation implicated in Lowe syndrome. The regional assignment of groups of YAC clones provides initiation points for further attempts to develop large cloned contiguous sequences, as well as material for investigation of regions involved in genetic diseases.

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Year:  1991        PMID: 2068096      PMCID: PMC52041          DOI: 10.1073/pnas.88.14.6157

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

1.  Cloning of human telomeres by complementation in yeast.

Authors:  S H Cross; R C Allshire; S J McKay; N I McGill; H J Cooke
Journal:  Nature       Date:  1989-04-27       Impact factor: 49.962

2.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

3.  Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq.

Authors:  A Ballabio; R Carrozzo; A Gil; B Gillard; N Affara; M A Ferguson-Smith; N Fraser; I Craig; M Rocchi; G Romeo
Journal:  Ann Hum Genet       Date:  1989-01       Impact factor: 1.670

4.  Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources.

Authors:  D L Nelson; S A Ledbetter; L Corbo; M F Victoria; R Ramírez-Solis; T D Webster; D H Ledbetter; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

5.  Genome linking with yeast artificial chromosomes.

Authors:  A Coulson; R Waterston; J Kiff; J Sulston; Y Kohara
Journal:  Nature       Date:  1988-09-08       Impact factor: 49.962

6.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

7.  Yeast artificial chromosomes with 200- to 800-kilobase inserts of human DNA containing HLA, V kappa, 5S, and Xq24-Xq28 sequences.

Authors:  R D Little; G Porta; G F Carle; D Schlessinger; M D'Urso
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

8.  Isolation of single-copy human genes from a library of yeast artificial chromosome clones.

Authors:  B H Brownstein; G A Silverman; R D Little; D T Burke; S J Korsmeyer; D Schlessinger; M V Olson
Journal:  Science       Date:  1989-06-16       Impact factor: 47.728

9.  Rapid screening of a human genomic library in yeast artificial chromosomes for single-copy sequences.

Authors:  C N Traver; S Klapholz; R W Hyman; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

10.  Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA.

Authors:  R A Gibbs; P N Nguyen; L J McBride; S M Koepf; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

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  14 in total

1.  High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.

Authors:  H E Steingruber; A Dunham; A J Coffey; S M Clegg; G R Howell; G L Maslen; C E Scott; R Gwilliam; P J Hunt; E C Sotheran; E J Huckle; S E Hunt; P Dhami; C Soderlund; M A Leversha; D R Bentley; M T Ross
Journal:  Genome Res       Date:  1999-08       Impact factor: 9.043

2.  A two-dimensional YAC pooling strategy for library screening via STS and Alu-PCR methods.

Authors:  C T Amemiya; M J Alegria-Hartman; C Aslanidis; C Chen; J Nikolic; J C Gingrich; P J de Jong
Journal:  Nucleic Acids Res       Date:  1992-05-25       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.  Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

Authors:  N Dahl; J Laporte; L Hu; V Biancalana; D Le Palier; D Cohen; C Piussan; J L Mandel
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

5.  Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors:  A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

6.  Fluorescent in-situ hybridization of cattle and sheep chromosomes with cloned human fragile-X DNA.

Authors:  Ahmad Ali; P D Thomsen; M E Babar
Journal:  Mol Biol Rep       Date:  2008-03-14       Impact factor: 2.316

7.  Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes.

Authors:  I Okabe; O Attree; L C Bailey; D L Nelson; R L Nussbaum
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

8.  Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiae.

Authors:  I Okabe; L C Bailey; O Attree; S Srinivasan; J M Perkel; B C Laurent; M Carlson; D L Nelson; R L Nussbaum
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

9.  Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.

Authors:  S A Ledbetter; A Kuwano; W B Dobyns; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

10.  Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions.

Authors:  A Chatterjee; T Tanaka; J E Parrish; G E Herman
Journal:  Mamm Genome       Date:  1995-11       Impact factor: 2.957

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