Literature DB >> 8703123

Molecular dissection of a cosmid from a gene-rich region in 17q21 and characterization of a candidate gene for alpha-N-acetylglucosaminidase with two cDNA isoforms.

Z Zhao1, A Yazdani, Y Shen, Z Sun, J Bailey, C T Caskey, C C Lee.   

Abstract

A cosmid mapped to human Chromosome (Chr) 17q21, c140c10, was found to contain a CpG island. We completed the sequence analysis of c140c10 because of two considerations: the cosmid contained an STS from the 17-beta-hydroxysteroid dehydrogenase gene (17-HSD), which was believed to be a neighbor of the breast cancer susceptibility gene, BRCA1; CpG islands are usually associated downstream and/or upstream of human genes. Computer-based exon trapping of the cosmid sequence revealed putative additional exons. With two of those exons used as a probe to screen human placental cDNA libraries, two cDNA isoforms for a novel gene, designated as ufHSD, were isolated. The amino acid sequence of the open reading frames of the cDNA showed no significant homology to any protein in the data base. However, it is possible that our cDNAs are from the gene for alpha-acetylglucosaminidase, which has recently been localized to the same region. Northern analyses show that the major isoform is expressed in all tissues tested, with the highest expression in blood leukocytes and lowest in brain. Finally, our study has shown that the 46.7-kb cosmid c140c10 encompasses loci for five genes and pseudo-genes: PsiPTP4A, ufHSD, 17-HSDI, 17-HSDII, and 22A1.

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Year:  1996        PMID: 8703123     DOI: 10.1007/s003359900206

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  13 in total

1.  CpG islands as gene markers in the human genome.

Authors:  F Larsen; G Gundersen; R Lopez; H Prydz
Journal:  Genomics       Date:  1992-08       Impact factor: 5.736

2.  Characterization and genomic mapping of genes and pseudogenes of a new human protein tyrosine phosphatase.

Authors:  Z Zhao; C C Lee; D G Monckton; A Yazdani; M I Coolbaugh; X Li; J Bailey; Y Shen; C T Caskey
Journal:  Genomics       Date:  1996-07-01       Impact factor: 5.736

3.  CpG islands in vertebrate genomes.

Authors:  M Gardiner-Garden; M Frommer
Journal:  J Mol Biol       Date:  1987-07-20       Impact factor: 5.469

4.  A new method for predicting signal sequence cleavage sites.

Authors:  G von Heijne
Journal:  Nucleic Acids Res       Date:  1986-06-11       Impact factor: 16.971

5.  Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid libraries.

Authors:  C C Lee; A Yazdani; M Wehnert; Z Y Zhao; E A Lindsay; J Bailey; M I Coolbaugh; L Couch; M Xiong; A C Chinault
Journal:  Hum Mol Genet       Date:  1995-08       Impact factor: 6.150

6.  Linkage of early-onset familial breast cancer to chromosome 17q21.

Authors:  J M Hall; M K Lee; B Newman; J E Morrow; L A Anderson; B Huey; M C King
Journal:  Science       Date:  1990-12-21       Impact factor: 47.728

7.  Purification and kinetic parameters of bovine liver N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase.

Authors:  K G Mullis; M Huynh; R H Kornfeld
Journal:  J Biol Chem       Date:  1994-01-21       Impact factor: 5.157

8.  Adaptor-based uracil DNA glycosylase cloning simplifies shotgun library construction for large-scale sequencing.

Authors:  B Andersson; C M Povinelli; M A Wentland; Y Shen; D M Muzny; R A Gibbs
Journal:  Anal Biochem       Date:  1994-05-01       Impact factor: 3.365

9.  High-density genetic map of the BRCA1 region of chromosome 17q12-q21.

Authors:  L A Anderson; L Friedman; S Osborne-Lawrence; E Lynch; J Weissenbach; A Bowcock; M C King
Journal:  Genomics       Date:  1993-09       Impact factor: 5.736

10.  The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.

Authors:  Z Zhao; C C Lee; S Jiralerspong; R C Juyal; F Lu; A Baldini; F Greenberg; C T Caskey; P I Patel
Journal:  Hum Mol Genet       Date:  1995-04       Impact factor: 6.150

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  2 in total

1.  Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase.

Authors:  H H Li; W H Yu; N Rozengurt; H Z Zhao; K M Lyons; S Anagnostaras; M S Fanselow; K Suzuki; M T Vanier; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-07       Impact factor: 11.205

2.  NAGLU mutations underlying Sanfilippo syndrome type B.

Authors:  A Schmidtchen; D Greenberg; H G Zhao; H H Li; Y Huang; P Tieu; H Z Zhao; S Cheng; Z Zhao; C B Whitley; P Di Natale; E F Neufeld
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

  2 in total

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