Literature DB >> 2921028

Lack of complementation between xeroderma pigmentosum complementation groups D and H.

R T Johnson1, G C Elliott, S Squires, V C Joysey.   

Abstract

The construction of permanent hybrid cell lines between xeroderma pigmentosum (XP) cells from different complementation groups allows analysis not only of the degree of repair correction but also of the restoration of biological activity to the UV-irradiated cells. With use of an immortal human cell line (HD2) that expresses excision repair defects typical of XP group D, a series of permanent hybrid cells has been produced with XP cells from groups A to H. Excision repair, as measured by incision analysis and unscheduled DNA synthesis, is restored to normal or near normal levels in crosses involving HD2 and cells from XP groups A, B, C, E, F, G, and I. All these hybrids show complementation for the recovery of normal UV resistance. As expected, hybrids expressing poor incision and hypersensitivity to UV were produced in crosses between HD2 and XPD fibroblasts, but they were also produced without exception when XPH was the partner. In the permanent HD2 x XPD or XPH hybrids, analysis of incision capacity reveals abnormally low activity and therefore that there has been no complementation. The true hybrid nature of HD2 x XPH cells has been confirmed by HL-A and -B tissue typing; moreover, detailed kinetic analysis of incision in these cells shows that the XPH phenotype, rather than the XPD, is expressed, i.e. breaks accumulate at low UV fluence of 1 J/m2. To help confirm these findings, another immortal XPD cell line was used in fusions involving HD2, XPH, or XPI. Cells resistant to ultraviolet were produced only with XPI fibroblasts. These data are discussed in terms of whether XPD and H mutations are likely to be allelic with respect to incision.

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Year:  1989        PMID: 2921028     DOI: 10.1007/BF00278989

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


  18 in total

1.  Abnormal kinetics of DNA synthesis in ultraviolet light-irradiated cells from patients with Cockayne's syndrome.

Authors:  A R Lehmann; S Kirk-Bell; L Mayne
Journal:  Cancer Res       Date:  1979-10       Impact factor: 12.701

2.  Complementing xeroderma pigmentosum fibroblasts restore biological activity to UV-damaged DNA.

Authors:  R S Day; K H Kraemer; J H Robbins
Journal:  Mutat Res       Date:  1975-05       Impact factor: 2.433

3.  DNA repair monitored by an enzymatic assay in multinucleate xeroderma pigmentosum cells after fusion.

Authors:  M C Paterson; P H Lohman; A Westerveld; M L Sluyter
Journal:  Nature       Date:  1974-03-01       Impact factor: 49.962

4.  Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.

Authors:  J H Robbins; K H Kraemer; M A Lutzner; B W Festoff; H G Coon
Journal:  Ann Intern Med       Date:  1974-02       Impact factor: 25.391

5.  Three complementation groups in Cockayne syndrome.

Authors:  A R Lehmann
Journal:  Mutat Res       Date:  1982-12       Impact factor: 2.433

6.  Approaches to the quantitative analysis of repair through the use of inhibitors.

Authors:  C S Downes
Journal:  Nucleic Acids Symp Ser       Date:  1984

7.  Expression and segregation of HL-A antigens in D98/AH-2 by lymphocyte and fibroblast hybrids.

Authors:  R H Kennett; B Hampshire; B Bengtsson; W F Bodmer
Journal:  Tissue Antigens       Date:  1975-08

8.  [Photosensitization and DNA repair. Possible nosologic relationship between Xeroderma pigmentosum and Cockayne's syndrome].

Authors:  D Lafforet; J M Dupuy
Journal:  Arch Fr Pediatr       Date:  1978-12

9.  Differences in patterns of complementation of the more common groups of xeroderma pigmentosum: possible implications.

Authors:  F Giannelli; S A Pawsey; J A Avery
Journal:  Cell       Date:  1982-06       Impact factor: 41.582

10.  Xeroderma pigmentosum D-HeLa hybrids with low and high ultraviolet sensitivity associated with normal and diminished DNA repair ability, respectively.

Authors:  R T Johnson; S Squires; G C Elliott; G L Koch; A J Rainbow
Journal:  J Cell Sci       Date:  1985-06       Impact factor: 5.285

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  14 in total

1.  Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D.

Authors:  J H Robbins
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

2.  Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiation.

Authors:  A R Lehmann; A F Thompson; S A Harcourt; M Stefanini; P G Norris
Journal:  J Med Genet       Date:  1993-08       Impact factor: 6.318

3.  Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.

Authors:  W L Flejter; L D McDaniel; D Johns; E C Friedberg; R A Schultz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

4.  Molecular cloning of the human DNA excision repair gene ERCC-6.

Authors:  C Troelstra; H Odijk; J de Wit; A Westerveld; L H Thompson; D Bootsma; J H Hoeijmakers
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

5.  No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H.

Authors:  J H Robbins
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

6.  DNA.RNA helicase activity of RAD3 protein of Saccharomyces cerevisiae.

Authors:  V Bailly; P Sung; L Prakash; S Prakash
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

7.  Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.

Authors:  G Weeda; L B Ma; R C van Ham; A J van der Eb; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1991-11-25       Impact factor: 16.971

8.  The Schizosaccharomyces pombe rhp3+ gene required for DNA repair and cell viability is functionally interchangeable with the RAD3 gene of Saccharomyces cerevisiae.

Authors:  P R Reynolds; S Biggar; L Prakash; S Prakash
Journal:  Nucleic Acids Res       Date:  1992-05-11       Impact factor: 16.971

9.  Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

Authors:  W Vermeulen; J Jaeken; N G Jaspers; D Bootsma; J H Hoeijmakers
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

Review 10.  Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.

Authors:  B C Broughton; A F Thompson; S A Harcourt; W Vermeulen; J H Hoeijmakers; E Botta; M Stefanini; M D King; C A Weber; J Cole
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

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