Literature DB >> 2339699

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus.

J C Myers1, T A Jones, E R Pohjolainen, A S Kadri, A D Goddard, D Sheer, E Solomon, T Pihlajaniemi.   

Abstract

Type IV collagen is a major structural component of basement membranes. Four constituent polypeptides have been described and characterized to different degrees. Whereas the primary structure of the alpha 1(IV) and alpha 2(IV) chains has been completely established, only short protein sequences have been reported for the recently recognized alpha 3(IV) and alpha 4(IV) subunits. We have isolated overlapping human cDNA clones whose derived amino acid sequence is highly homologous to the alpha 1(IV) and alpha 2(IV) chains. However, these clones code for neither alpha 3(IV) nor alpha 4(IV), and thus this new polypeptide has been designated the alpha 5 chain of type IV collagen. To determine whether the gene encoding the alpha 5(IV) chain is syntenic with the contiguously arranged alpha 1(IV) and alpha 2(IV) genes at 13q34, the alpha 5(IV) cloned DNA was hybridized to genomic DNA from somatic cell hybrids and to metaphase chromosomes. The results demonstrated that the alpha 5(IV) collagen gene is located on the long arm of the X chromosome. Since 14 collagen genes have previously been assigned to nine autosomes, these data represent the first mapping of a collagen gene to the X chromosome. Most important, the alpha 5(IV) gene has been sublocalized to bands Xq22----q23, which are in the same region known to contain the locus for the X-linked form of Alport syndrome. It is therefore possible that this severe dominantly inherited nephritis, manifested by splitting of the glomerular basement membrane, could be caused by mutations in the alpha 5(IV) collagen gene.

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Year:  1990        PMID: 2339699      PMCID: PMC1683837     

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


  50 in total

1.  Assignment of the gene coding for the alpha 1 chain of collagen type XIII (COL13A1) to human chromosome region 10q11----qter.

Authors:  L Pajunen; M Tamminen; E Solomon; T Pihlajaniemi
Journal:  Cytogenet Cell Genet       Date:  1989

2.  Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13.

Authors:  V van Heyningen; M Bobrow; W F Bodmer; S E Gardiner; S Povey; D A Hopkinson
Journal:  Ann Hum Genet       Date:  1975-01       Impact factor: 1.670

3.  A cytochrome P-450 gene family mapped to human chromosome 19.

Authors:  I R Phillips; E A Shephard; S Povey; M B Davis; G Kelsey; M Monteiro; L F West; J Cowell
Journal:  Ann Hum Genet       Date:  1985-10       Impact factor: 1.670

4.  Genetic heterogeneity of Alport syndrome.

Authors:  J Feingold; E Bois; A Chompret; M Broyer; M C Gubler; J P Grünfeld
Journal:  Kidney Int       Date:  1985-04       Impact factor: 10.612

5.  Differential Giemsa staining of sister chromatids and the study of chromatid exchanges without autoradiography.

Authors:  S Wolff; P Perry
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

6.  Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.

Authors:  M E Harper; G F Saunders
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

7.  Hereditary nephropathy (Alport syndrome): correlation of clinical data with glomerular basement membrane alterations.

Authors:  H J Rumpelt
Journal:  Clin Nephrol       Date:  1980-05       Impact factor: 0.975

8.  Human myosin heavy chain genes assigned to chromosome 17 using a human cDNA clone as probe.

Authors:  Y H Edwards; M Parkar; S Povey; L F West; J M Parrington; E Solomon
Journal:  Ann Hum Genet       Date:  1985-05       Impact factor: 1.670

9.  Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16.

Authors:  S Povey; S J Jeremiah; R F Barker; D A Hopkinson; E B Robson; P J Cook; E Solomon; M Bobrow; B Carritt; K E Buckton
Journal:  Ann Hum Genet       Date:  1980-01       Impact factor: 1.670

10.  Localization of the human procollagen alpha 1(IV) gene to chromosome 13q34 by in situ hybridization.

Authors:  B S Emanuel; B T Sellinger; L J Gudas; J C Myers
Journal:  Am J Hum Genet       Date:  1986-01       Impact factor: 11.025

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  22 in total

Review 1.  Glomerular diseases: genetic causes and future therapeutics.

Authors:  Chih-Kang Chiang; Reiko Inagi
Journal:  Nat Rev Nephrol       Date:  2010-07-20       Impact factor: 28.314

Review 2.  Type IV collagen-derived angiogenesis inhibitors.

Authors:  Thomas M Mundel; Raghu Kalluri
Journal:  Microvasc Res       Date:  2007-05-25       Impact factor: 3.514

3.  Alport syndrome caused by a 5' deletion within the COL4A5 gene.

Authors:  A Renieri; M Seri; J C Myers; T Pihlajaniemi; A Sessa; G Rizzoni; M De Marchi
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

Review 4.  Alport's syndrome.

Authors:  F Flinter
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

5.  Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13.

Authors:  A Toren; N Amariglio; G Rozenfeld-Granot; A J Simon; F Brok-Simoni; E Pras; G Rechavi
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

6.  Multipoint linkage analysis in X-linked Alport syndrome.

Authors:  J M Hertz; T A Kruse; A Thomsen; E S Spencer
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

7.  High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.

Authors:  D F Barker; P R Fain; D E Goldgar; J N Dietz-Band; A E Turco; C E Kashtan; M C Gregory; K Tryggvason; M H Skolnick; C L Atkin
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

8.  Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndrome.

Authors:  A Renieri; M Seri; L Galli; P Cosci; E Imbasciati; L Massella; G Rizzoni; G Restagno; A O Carbonara; E Stramignoni
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

9.  Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV.

Authors:  K Zheng; P S Thorner; P Marrano; R Baumal; R R McInnes
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

10.  Sequence and localization of a partial cDNA encoding the human alpha 3 chain of type IV collagen.

Authors:  K E Morrison; M Mariyama; T L Yang-Feng; S T Reeders
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

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