Literature DB >> 2163003

Characterization of human cDNA and genomic clones for glial fibrillary acidic protein.

M Brenner1, K Lampel, Y Nakatani, J Mill, C Banner, K Mearow, M Dohadwala, R Lipsky, E Freese.   

Abstract

Both a partial cDNA clone and a complete genomic clone have been isolated for human gfa, the gene encoding the major component of astrocyte intermediate filaments, glial fibrillary acidic protein (GFAP). The nucleotide sequence of the entire coding region and 102 bp of the 5' flanking DNA was determined. The mRNA start site was identified by primer extension and probe protection experiments, and a novel in vitro transcription and translation procedure was then used to establish that the first ATG in the mRNA initiates GFAP synthesis. The predicted amino-terminal sequence for human GFAP differs greatly from that previously deduced for mouse GFAP from its gene sequence, despite otherwise high homology. This discrepancy was resolved by determining that the published mouse genomic sequence has an incorrect additional base. The corrected sequence produces strong homology between human and mouse GFAP in their predicted amino acid sequences, and suggests that human and mouse GFAP initiate at homologous positions. The beginning sequence deduced here for both proteins is matched closely by that previously obtained for porcine GFAP by direct sequencing of its amino-terminal end. This supports the protein initiation sites proposed, and also indicates that GFAP is not processed at its amino-terminal end.

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Year:  1990        PMID: 2163003     DOI: 10.1016/0169-328x(90)90078-r

Source DB:  PubMed          Journal:  Brain Res Mol Brain Res        ISSN: 0169-328X


  16 in total

1.  Directed establishment of rat brain cell lines with the phenotypic characteristics of type 1 astrocytes.

Authors:  E H Radany; M Brenner; F Besnard; V Bigornia; J M Bishop; C F Deschepper
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

Review 2.  GFAP and its role in Alexander disease.

Authors:  Roy A Quinlan; Michael Brenner; James E Goldman; Albee Messing
Journal:  Exp Cell Res       Date:  2007-04-06       Impact factor: 3.905

Review 3.  An analysis of vertebrate mRNA sequences: intimations of translational control.

Authors:  M Kozak
Journal:  J Cell Biol       Date:  1991-11       Impact factor: 10.539

Review 4.  Interpreting cDNA sequences: some insights from studies on translation.

Authors:  M Kozak
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

5.  Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice.

Authors:  A Messing; M W Head; K Galles; E J Galbreath; J E Goldman; M Brenner
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

6.  The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27.

Authors:  Ming Der Perng; Mu Su; Shu Fang Wen; Rong Li; Terry Gibbon; Alan R Prescott; Michael Brenner; Roy A Quinlan
Journal:  Am J Hum Genet       Date:  2006-06-12       Impact factor: 11.025

7.  Human glial fibrillary acidic protein (GFAP): molecular cloning of the complete cDNA sequence and chromosomal localization (chromosome 17) of the GFAP gene.

Authors:  T Kumanishi; H Usui; T Ichikawa; A Nishiyama; T Katagiri; S Abe; Y Yoshida; K Washiyama; R Kuwano; K Sakimura
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

8.  An RNA polymerase II promoter containing sequences upstream and downstream from the RNA startpoint that direct initiation of transcription from the same site.

Authors:  Y Nakatani; M Brenner; E Freese
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

9.  Alterations in striatal glial fibrillary acidic protein expression in response to 6-hydroxydopamine-induced denervation.

Authors:  J G Sheng; S Shirabe; N Nishiyama; J P Schwartz
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

10.  Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin association.

Authors:  Ming-Der Perng; Shu-Fang Wen; Terry Gibbon; Jinte Middeldorp; Jacqueline Sluijs; Elly M Hol; Roy A Quinlan
Journal:  Mol Biol Cell       Date:  2008-08-06       Impact factor: 4.138

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