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PMID: 2666912 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

A human rel proto-oncogene cDNA containing an Alu fragment as a potential coding exon.

Oncogene ·Vol. 4 ·No. 7 ·1989-07-00 ·Pages 935-42

Brownell E, Mittereder N, Rice NR

Abstract

Two rel-containing cDNA clones were isolated from a library derived from the Daudi human cell line, which is known to express c-rel mRNA. Clone #1 appeared to contain the entire c-rel coding sequence, which differs from v-rel in having three additional N-terminal residues and 111 additional C-terminal residues. In addition, Clone #1 had an internal 32 amino acid exon not found in v-rel or in turkey c-rel. Clone #2 was truncated at its 5' end and did not contain this new exon. Analysis of a genomic clone of human c-rel revealed that the new exon was a portion of an inverted Alu repeat. The occurrence of potential splice sites and of open reading frames in the inverted consensus Alu sequence suggests that the incorporation of Alu fragments as potential coding exons could be a relatively common event in human mRNAs. Whether such messages can be translated is unknown: antiserum raised against a peptide at the predicted C-terminus of the c-rel protein precipitated p82hc-rel, but antiserum raised against a peptide located in the Alu exon did not.

MeSH Terms
Base Sequence DNA/analysis Exons Humans Molecular Sequence Data Protein Biosynthesis Proto-Oncogene Mas Proto-Oncogene Proteins/analysis,genetics Proto-Oncogene Proteins c-rel Proto-Oncogenes Repetitive Sequences, Nucleic Acid
Chemicals
MAS1 protein, human Proto-Oncogene Mas Proto-Oncogene Proteins Proto-Oncogene Proteins c-rel DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brownell E
Laboratory of Molecular Virology and Carcinogenesis, NCI-Frederick Cancer Research Facility, Maryland 21701.
Mittereder N
Rice N R
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1989-07-00
Pages
935-42
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · N01-CO-74101 · United States
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