Literature DB >> 2888721

A hypervariable repeated sequence on human chromosome 1p36.

N Buroker1, R Bestwick, G Haight, R E Magenis, M Litt.   

Abstract

When used to probe Southern blots of TaqI-digested DNAs from unrelated individuals, p1-79, a 900 bp subclone of a random human cosmid, revealed at least 50 fragments, many of which were polymorphic. Each of 27 unrelated individuals tested with p1-79 displayed a distinct band pattern. Similar variation was seen with several other enzymes, including HaeIII, MspI, PstI and PvuII, whereas other enzymes yielded primarily large fragments of greater than 40 kb. In situ hybridization of p1-79 showed that the loci of hybridization are clustered on human chromosome band 1p36; localization of all TaqI fragments to chromosome 1 was confirmed with a human-rodent somatic cell hybrid panel. DNA sequencing of p1-79 revealed several copies of a 39 bp repeat whose variation in copy number might be the basis of the observed length polymorphisms. Studies of 3-generation Utah families suggest that the numerous restriction fragments homologous to p1-79 are inherited as haplotypes, implying that recombination within this cluster of loci is rare and allowing the cluster to serve as a useful marker for human gene mapping.

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Year:  1987        PMID: 2888721     DOI: 10.1007/bf00272388

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  22 in total

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Authors:  H J Cooke; W R Brown; G A Rappold
Journal:  Nature       Date:  1985 Oct 24-30       Impact factor: 49.962

2.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

3.  U1 small nuclear RNA genes are located on human chromosome 1 and are expressed in mouse-human hybrid cells.

Authors:  E Lund; C Bostock; M Robertson; S Christie; J L Mitchen; J E Dahlberg
Journal:  Mol Cell Biol       Date:  1983-12       Impact factor: 4.272

4.  Highly variable regions of DNA flank the human alpha globin genes.

Authors:  D R Higgs; S E Goodbourn; J S Wainscoat; J B Clegg; D J Weatherall
Journal:  Nucleic Acids Res       Date:  1981-09-11       Impact factor: 16.971

5.  Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue.

Authors:  D J Capon; E Y Chen; A D Levinson; P H Seeburg; D V Goeddel
Journal:  Nature       Date:  1983-03-03       Impact factor: 49.962

6.  New M13 vectors for cloning.

Authors:  J Messing
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

7.  The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

Authors:  G I Bell; M J Selby; W J Rutter
Journal:  Nature       Date:  1982-01-07       Impact factor: 49.962

8.  Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q.

Authors:  N E Buroker; R E Magenis; K Weliky; G Bruns; M Litt
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

9.  A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid.

Authors:  M Litt; R Sheehy; G A Bruns; R E Magenis
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

10.  Restriction fragment length polymorphisms as markers of engraftment in allogeneic marrow transplantation.

Authors:  B R Blazar; H T Orr; D C Arthur; J H Kersey; A H Filipovich
Journal:  Blood       Date:  1985-12       Impact factor: 22.113

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  26 in total

1.  Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.

Authors:  H Dannenberg; E J Speel; J Zhao; P Saremaslani; E van Der Harst; J Roth; P U Heitz; H J Bonjer; W N Dinjens; W J Mooi; P Komminoth; R R de Krijger
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

2.  Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA.

Authors:  Michelle L Duquette; Priya Handa; Jack A Vincent; Andrew F Taylor; Nancy Maizels
Journal:  Genes Dev       Date:  2004-07-01       Impact factor: 11.361

3.  Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locus.

Authors:  J Groden; J German
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

Review 4.  Interphase cytogenetics.

Authors:  C S Herrington; J O McGee
Journal:  Neurochem Res       Date:  1990-04       Impact factor: 3.996

Review 5.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

6.  Duplication of a genomic region containing the Cdc2L1-2 and MMP21-22 genes on human chromosome 1p36.3 and their linkage to D1Z2.

Authors:  R Gururajan; J M Lahti; J Grenet; J Easton; I Gruber; P F Ambros; V J Kidd
Journal:  Genome Res       Date:  1998-09       Impact factor: 9.043

7.  Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Authors:  S K Shapira; C McCaskill; H Northrup; A S Spikes; F F Elder; V R Sutton; J R Korenberg; F Greenberg; L G Shaffer
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 8.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

9.  Probe walking: development of novel probes for DNA fingerprinting.

Authors:  K Washio; S Misawa; S Ueda
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

10.  Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization.

Authors:  B Trask; G van den Engh; D Pinkel; J Mullikin; F Waldman; H van Dekken; J Gray
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

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