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PMID: 6308118 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Sequence and structure of the coding region of the human H-ras-1 gene from T24 bladder carcinoma cells.

Journal of molecular and applied genetics ·Vol. 2 ·No. 2 ·1983-00-00 ·Pages 173-80

Fasano O, Taparowsky E, Fiddes J, Wigler M, Goldfarb M

Abstract

We have molecularly cloned and sequenced cDNA to the transcript of H-ras-1, the transforming gene of the T24 human bladder carcinoma cell line. The transcript derives from at least five exons in the H-ras-1 gene, and RNA splicing occurs at sites typical of exon-intron junctions. T24 H-ras-1 RNA has an AUG-initiated open reading frame of 567 nucleotides, which can encode a protein of mass comparable to the apparent molecular weight of the T24 H-ras-1 gene product. The T24 H-ras-1 gene product is nearly identical to v-H-ras p21, the transforming protein encoded by the genome of Harvey sarcoma virus. We discuss the implications of this sequence conservation in the structure-function relationships of ras proteins.

MeSH Terms
Base Sequence Cell Line Cloning, Molecular DNA/genetics DNA, Neoplasm/genetics DNA, Viral/genetics Genes Genes, Viral Humans Sarcoma Viruses, Murine/genetics Transformation, Genetic Urinary Bladder Neoplasms/genetics
Chemicals
DNA, Neoplasm DNA, Viral DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Fasano O
Taparowsky E
Fiddes J
Wigler M
Goldfarb M
Article Info
Journal
Journal of molecular and applied genetics
Abbr.
J Mol Appl Genet
ISSN
0271-6801
Published
1983-00-00
Pages
173-80
Language
English
Region
United States
NLM ID
8109497
Subset
IM
Databases
GENBANK
J00206, J00276, J00277, K00954
External Links
PubMed source
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