Literature DB >> 6093508

Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis.

T S Su, R L Nussbaum, S Airhart, D H Ledbetter, T Mohandas, W E O'Brien, A L Beaudet.   

Abstract

There are multiple, processed, dispersed pseudogenes for human argininosuccinate synthetase. Chinese hamster X human somatic cell hybrids were used to map DNA fragment groups corresponding to the single expressed gene and 14 pseudogene loci. Each chromosomal assignment was confirmed using hybrids containing very few human chromosomes and/or by demonstrating monosomic or trisomic dosage in human cell lines with chromosomal abnormalities. Pseudogenes were mapped to chromosomes 2cen-p25, 3q12-qter, 4q21-qter, 5 (two loci), 6, 7, 9p13-q11, 9q11-q22, 11q, 12, Xp22-pter, Xq22-q26, and Ycen-q11. DNA fragments from the expressed gene were mapped to 9q34-qter in agreement with the previous assignment for enzyme activity. A high-frequency restriction fragment length polymorphism mapped to 9q11-q22. The analyses emphasized the feasibility of using chromosomally abnormal human cell lines for confirmation and regionalization of gene-mapping assignments made using somatic-cell hybrids. Conversely, cloned DNA probes, once mapped and characterized, can be very valuable for determining the chromosomal composition of interspecies hybrids and the dosage of loci in human cells. The argininosuccinate synthetase cDNA is a convenient reagent for dosage analysis of 15 human loci on 11 different chromosomes. Improved reagents could be designed that would simplify Southern blot patterns by eliminating overlapping DNA fragments and providing a single DNA fragment for each locus.

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Year:  1984        PMID: 6093508      PMCID: PMC1684515     

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


  12 in total

1.  Transformation of mammalian cells with genes from procaryotes and eucaryotes.

Authors:  M Wigler; R Sweet; G K Sim; B Wold; A Pellicer; E Lacy; T Maniatis; S Silverstein; R Axel
Journal:  Cell       Date:  1979-04       Impact factor: 41.582

2.  Regional asssignments of the loci AK3, ACONS, and ASS on human chromosome 9.

Authors:  B Carritt; S Povey
Journal:  Cytogenet Cell Genet       Date:  1979

3.  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

4.  Cloning of cDNA for argininosuccinate synthetase mRNA and study of enzyme overproduction in a human cell line.

Authors:  T S Su; H G Bock; W E O'Brien; A L Beaudet
Journal:  J Biol Chem       Date:  1981-11-25       Impact factor: 5.157

5.  Dispersion of argininosuccinate-synthetase-like human genes to multiple autosomes and the X chromosome.

Authors:  A L Beaudet; T S Su; W E O'Brien; P D'Eustachio; P E Barker; F H Ruddle
Journal:  Cell       Date:  1982-08       Impact factor: 41.582

6.  Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase.

Authors:  S P Daiger; R S Wildin; T S Su
Journal:  Nature       Date:  1982-08-12       Impact factor: 49.962

7.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

8.  Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids. (With 1 color plate).

Authors:  B Alhadeff; M Velivasakis; M Siniscalco
Journal:  Cytogenet Cell Genet       Date:  1977

9.  Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations.

Authors:  T Mohandas; R S Sparkes; M C Sparkes; J D Shulkin; K E Toomey; S J Funderburk
Journal:  Am J Hum Genet       Date:  1979-09       Impact factor: 11.025

10.  A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

Authors:  R L Nussbaum; W E Crowder; W L Nyhan; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1983-07       Impact factor: 11.205

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  21 in total

1.  CA repeat polymorphism at the ASS locus.

Authors:  M A Yuille; R M Hampson; R M Harris; N A Affara; J R Yates; M A Ferguson-Smith
Journal:  Nucleic Acids Res       Date:  1990-12-25       Impact factor: 16.971

Review 2.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferase.

Authors:  M G Humphreys-Beher; B Bunnell; P vanTuinen; D H Ledbetter; V J Kidd
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

4.  Deletion mapping of human chromosome 5 using chromosome-specific DNA probes.

Authors:  L R Carlock; D Skarecky; S L Dana; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

5.  The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1.

Authors:  M E Goode; P vanTuinen; D H Ledbetter; S P Daiger
Journal:  Am J Hum Genet       Date:  1986-04       Impact factor: 11.025

6.  Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.

Authors:  P I Patel; B Franco; C Garcia; S A Slaugenhaupt; Y Nakamura; D H Ledbetter; A Chakravarti; J R Lupski
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

7.  Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.

Authors:  Brian P Chadwick
Journal:  Chromosome Res       Date:  2019-11-27       Impact factor: 5.239

8.  A chromosome 11-linked determinant controls fetal globin expression and the fetal-to-adult globin switch.

Authors:  M Melis; G Demopulos; V Najfeld; J W Zhang; M Brice; T Papayannopoulou; G Stamatoyannopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

9.  Nature and frequency of mutations in the argininosuccinate synthetase gene that cause classical citrullinemia.

Authors:  K Kobayashi; H Kakinoki; T Fukushige; N Shaheen; H Terazono; T Saheki
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

10.  Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

Authors:  P vanTuinen; W B Dobyns; D C Rich; K M Summers; T J Robinson; Y Nakamura; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

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