Literature DB >> 6583157

Assignment of the gene for cystathionine beta-synthase to human chromosome 21 in somatic cell hybrids.

F Skovby, N Krassikoff, U Francke.   

Abstract

Among several established mouse, rat, and Chinese hamster cell lines that were screened for cystathionine beta-synthase (CBS) activity, mouse 3T3 and Chinese hamster Don fibroblasts were found to contain no detectable activity. Somatic cell hybrids between human fibroblasts KG-7 with normal CBS activity and Don/a23TK- cells (series XXI) were examined for CBS activity and for human chromosome content. Only chromosome 21 cosegregated with CBS activity. Because the activities measured could represent either Chinese hamster or human gene products, we have prepared a new series of hybrids between Don/a23TK- cells and mutant human fibroblasts from a patient with homocystinuria due to deficiency of functional CBS mRNA. None of these (series XXV) hybrids contained detectable CBS activity, although collectively all human chromosomes were represented. Our results suggest that the human gene for CBS, called CBS, and thus for the most common form of homocystinuria, is located on chromosome 21.

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Year:  1984        PMID: 6583157     DOI: 10.1007/bf00286520

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


  17 in total

1.  Genetic control of mitochondrial enzymes in human-mouse somatic cell hybrids.

Authors:  V Van Heyningen; I Craig; W Bodmer
Journal:  Nature       Date:  1973-04-20       Impact factor: 49.962

2.  Prenatal diagnosis of homocystinuria.

Authors:  B Fowler; A L Børresen; N Boman
Journal:  Lancet       Date:  1982-10-16       Impact factor: 79.321

3.  Biosynthesis and proteolytic activation of cystathionine beta-synthase in rat liver.

Authors:  F Skovby; J P Kraus; L E Rosenberg
Journal:  J Biol Chem       Date:  1984-01-10       Impact factor: 5.157

4.  The human genome through the eyes of a clinical geneticist.

Authors:  V A McKusick
Journal:  Cytogenet Cell Genet       Date:  1982

5.  Genetic control of cobalamin binding in normal and mutant cells: assignment of the gene for 5-methyltetrahydrofolate:L-homocysteine S-methyltransferase to human chromosome 1.

Authors:  I S Mellman; P F Lin; F H Ruddle; L E Rosenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

6.  Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity.

Authors:  J M Freeman; J D Finkelstein; S H Mudd
Journal:  N Engl J Med       Date:  1975-03-06       Impact factor: 91.245

7.  Homocystinuria: heterozygote detection using phytohemagglutinin-stimulated lymphocytes.

Authors:  J L Goldstein; B K Campbell; S M Gartler
Journal:  J Clin Invest       Date:  1973-01       Impact factor: 14.808

8.  Homocystinuria: biogenesis of cystathionine beta-synthase subunits in cultured fibroblasts and in an in vitro translation system programmed with fibroblast messenger RNA.

Authors:  F Skovby; J P Kraus; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  Immunochemical studies on cultured fibroblasts from patients with homocystinuria due to cystathionine beta-synthase deficiency.

Authors:  F Skovby; J Kraus; C Redlich; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1982-01       Impact factor: 11.025

10.  Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunits.

Authors:  J Kraus; S Packman; B Fowler; L E Rosenberg
Journal:  J Biol Chem       Date:  1978-09-25       Impact factor: 5.157

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  18 in total

1.  Homocysteine and the methotrexate toxicity in trisomy 21.

Authors:  J Lejeune; M Peeters; M O Rethore; M C de Blois
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

2.  Homocysteinaemia and coronary atherosclerosis.

Authors:  T O Cheng
Journal:  Heart       Date:  1997-04       Impact factor: 5.994

3.  A direct regulatory interaction between chaperonin TRiC and stress-responsive transcription factor HSF1.

Authors:  Daniel W Neef; Alex M Jaeger; Rocio Gomez-Pastor; Felix Willmund; Judith Frydman; Dennis J Thiele
Journal:  Cell Rep       Date:  2014-10-30       Impact factor: 9.423

4.  Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.

Authors:  M L Van Keuren; P C Watkins; H A Drabkin; E W Jabs; J F Gusella; D Patterson
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

5.  Partial deletion 21: case report with biochemical studies and review.

Authors:  N J Carpenter; J S Mayes; B Say; D P Wilson
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

Review 6.  Hyperhomocysteinaemia; with reference to its neuroradiological aspects.

Authors:  M van den Berg; M S van der Knaap; G H Boers; C D Stehouwer; J A Rauwerda; J Valk
Journal:  Neuroradiology       Date:  1995-07       Impact factor: 2.804

Review 7.  Komrower Lecture. Molecular basis of phenotype expression in homocystinuria.

Authors:  J P Kraus
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

8.  Comparison of the 5' end of the rat and mouse cystathionine beta-synthase genes.

Authors:  M D Roper; J R Straubhaar; E Kraus; J Sokolová; M Hrebícek; J P Kraus
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

Review 9.  Classical homocystinuria: vascular risk and its prevention.

Authors:  S Yap
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 10.  Molecular genetics of human chromosome 21.

Authors:  P C Watkins; R E Tanzi; S V Cheng; J F Gusella
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

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