Literature DB >> 1672285

The exon-intron organization of the human erythrocyte alpha-spectrin gene.

L Kotula1, L D Laury-Kleintop, L Showe, K Sahr, A J Linnenbach, B Forget, P J Curtis.   

Abstract

The human erythrocyte alpha-spectrin gene which spans 80 kbp has been cloned from human genomic DNA as overlapping lambda recombinants. The exon-intron junctions were identified and the exons mapped. The gene is encoded by 52 exons whose sizes range from 684 bp to the smallest of 18 bp. The donor and acceptor splice site sequences match the splice site consensus sequences, with the exception of one splice site where a donor sequence begins with -GC. The size and location of exons do not correlate with the 106-amino-acid repeat, except in three locations where the surrounding codons are conserved as well. The lack of correspondence between exons and 106-amino-acid repeat is interpreted to reflect the appearance of a spectrin-like gene from a minigene early in the evolution of eukaryotes. Since current evidence indicates that introns were present in genes before the divergence of prokaryotes and eukaryotes, it is possible that the original distribution of introns within the minigene has been lost by the random deletion of introns from the spectrin gene.

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Year:  1991        PMID: 1672285     DOI: 10.1016/0888-7543(91)90230-c

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  7 in total

1.  Genomic anatomy of a premier major histocompatibility complex paralogous region on chromosome 1q21-q22.

Authors:  T Shiina; A Ando; Y Suto; F Kasai; A Shigenari; N Takishima; E Kikkawa; K Iwata; Y Kuwano; Y Kitamura; Y Matsuzawa; K Sano; M Nogami; H Kawata; S Li; Y Fukuzumi; M Yamazaki; H Tashiro; G Tamiya; A Kohda; K Okumura; T Ikemura; E Soeda; N Mizuki; M Kimura; S Bahram; H Inoko
Journal:  Genome Res       Date:  2001-05       Impact factor: 9.043

2.  A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.

Authors:  Daniel B Costa; Larisa Lozovatsky; Patrick G Gallagher; Bernard G Forget
Journal:  Blood       Date:  2005-09-08       Impact factor: 22.113

3.  The complete sequence of Drosophila beta-spectrin reveals supra-motifs comprising eight 106-residue segments.

Authors:  T J Byers; E Brandin; R A Lue; E Winograd; D Branton
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-01       Impact factor: 11.205

4.  Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.

Authors:  R Wilmotte; J Maréchal; L Morlé; F Baklouti; N Philippe; R Kastally; L Kotula; J Delaunay; N Alloisio
Journal:  J Clin Invest       Date:  1993-05       Impact factor: 14.808

5.  Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.

Authors:  P G Gallagher; L Kotula; Y Wang; S L Marchesi; P J Curtis; D W Speicher; B G Forget
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

6.  The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.

Authors:  M L Bloom; T M Kaysser; C S Birkenmeier; J E Barker
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-11       Impact factor: 11.205

7.  Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B.

Authors:  C Troelstra; W Hesen; D Bootsma; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1993-02-11       Impact factor: 16.971

  7 in total

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