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PMID: 8661052 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Localization and physical mapping of genes encoding the A+U-rich element RNA-binding protein AUF1 to human chromosomes 4 and X.

Genomics ·Vol. 34 ·No. 2 ·1996-06-01 ·Pages 219-22

Wagner BJ, Long L, Rao PN, Pettenati MJ, Brewer G

Abstract

Messenger RNAs encoding many oncoproteins and cytokines are relatively unstable. Their instability, which ensures appropriate levels and timing of expression, is controlled in part by proteins that bind to A+U-rich instability elements (AREs) present in the 3'-untranslated regions of the mRNAs. cDNAs encoding the AUF1 family of ARE-binding proteins were cloned from human and murine cDNA libraries. In the present study monochromosomal somatic cell hybrids were used to localize two AUF1 loci to human chromosomes 4 and X. In situ hybridization analyses using P1 clones as probes identified the 4q21.1-q21.2 and Xq12 regions as the locations of the AUF1 genes.

MeSH Terms
Animals Base Composition Binding Sites Chromosome Mapping Chromosomes, Human, Pair 4 Cloning, Molecular DNA, Complementary Gene Library Heterogeneous Nuclear Ribonucleoprotein D0 Heterogeneous-Nuclear Ribonucleoprotein D Humans Hybrid Cells In Situ Hybridization, Fluorescence Mice RNA, Messenger/metabolism RNA-Binding Proteins/biosynthesis,genetics,metabolism Recombinant Proteins/biosynthesis,metabolism X Chromosome
Chemicals
DNA, Complementary HNRNPD protein, human Heterogeneous Nuclear Ribonucleoprotein D0 Heterogeneous-Nuclear Ribonucleoprotein D Hnrpd protein, mouse RNA, Messenger RNA-Binding Proteins Recombinant Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wagner B J
Department of Microbiology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina, 27157, USA.
Long L
Rao P N
Pettenati M J
Brewer G
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1996-06-01
Pages
219-22
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIDDK NIH HHS · F32 DK08589 · United States
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