scholarly journals An S1 nuclease-sensitive region in the first intron of human platelet-derived growth factor A-chain gene contains a negatively acting cell type-specific regulatory element

1994 ◽  
Vol 22 (3) ◽  
pp. 457-464 ◽  
Author(s):  
Zhao-Yi Wang ◽  
Nobuyoshi Masaharu ◽  
Qing-Qing Qiu ◽  
Yasuo Takimato ◽  
Thomas F. Deuel
1998 ◽  
Vol 273 (50) ◽  
pp. 33239-33246 ◽  
Author(s):  
Raymond S. Maul ◽  
Hongxing Zhang ◽  
James D. Reid ◽  
Nancy G. Pedigo ◽  
David M. Kaetzel

1988 ◽  
Vol 8 (2) ◽  
pp. 571-577 ◽  
Author(s):  
F Rorsman ◽  
M Bywater ◽  
T J Knott ◽  
J Scott ◽  
C Betsholtz

The human platelet-derived growth factor (PDGF) A-chain locus was characterized by restriction endonuclease analysis, and the nucleotide sequence of its exons was determined. Seven exons were identified, spanning approximately 22 kilobase pairs of genomic DNA. Alternative exon usage, identified by cDNA cloning, occurs in a human glioblastoma cell line and may give rise to two types of A-chain precursors with different C termini. The exon-intron arrangement was similar to that of the PDGF B-chain/sis locus and seemed to divide the precursor proteins into functional domains. Southern blot analysis of genomic DNA showed that a single PDGF A-chain gene was present in the human genome.


1991 ◽  
Vol 88 (5) ◽  
pp. 1686-1690 ◽  
Author(s):  
Y. Takimoto ◽  
Z. Y. Wang ◽  
K. Kobler ◽  
T. F. Deuel

1988 ◽  
Vol 8 (2) ◽  
pp. 571-577
Author(s):  
F Rorsman ◽  
M Bywater ◽  
T J Knott ◽  
J Scott ◽  
C Betsholtz

The human platelet-derived growth factor (PDGF) A-chain locus was characterized by restriction endonuclease analysis, and the nucleotide sequence of its exons was determined. Seven exons were identified, spanning approximately 22 kilobase pairs of genomic DNA. Alternative exon usage, identified by cDNA cloning, occurs in a human glioblastoma cell line and may give rise to two types of A-chain precursors with different C termini. The exon-intron arrangement was similar to that of the PDGF B-chain/sis locus and seemed to divide the precursor proteins into functional domains. Southern blot analysis of genomic DNA showed that a single PDGF A-chain gene was present in the human genome.


1990 ◽  
Vol 10 (11) ◽  
pp. 6051-6054 ◽  
Author(s):  
R M Young ◽  
A E Mendoza ◽  
T Collins ◽  
S H Orkin

Two platelet-derived growth factor A-chain proteins, termed short and long A chains, are generated as a result of alternative mRNA splicing of exon 6 of the A-chain gene. S1 nuclease mapping and polymerase chain reaction analyses demonstrate that both short and long A-chain transcripts are expressed in a variety of normal tissues. In addition, immunohistochemical localization of long A-chain protein reveals a cellular distribution identical to that observed with platelet-derived growth factor heteroserum.


1990 ◽  
Vol 10 (11) ◽  
pp. 6051-6054
Author(s):  
R M Young ◽  
A E Mendoza ◽  
T Collins ◽  
S H Orkin

Two platelet-derived growth factor A-chain proteins, termed short and long A chains, are generated as a result of alternative mRNA splicing of exon 6 of the A-chain gene. S1 nuclease mapping and polymerase chain reaction analyses demonstrate that both short and long A-chain transcripts are expressed in a variety of normal tissues. In addition, immunohistochemical localization of long A-chain protein reveals a cellular distribution identical to that observed with platelet-derived growth factor heteroserum.


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