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PMID: 9178771 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning of a gene highly overexpressed in cancer coding for a novel KH-domain containing protein.

Oncogene ·Vol. 14 ·No. 22 ·1997-06-05 ·Pages 2729-33

Müeller-Pillasch F, Lacher U, Wallrapp C, Micha A, Zimmerhackl F, Hameister H, Varga G, Friess H, Büchler M, Beger HG, Vila MR, Adler G, Gress TM

Abstract

In a previous large scale screen for differentially expressed genes in pancreatic cancer, we identified a gene highly overexpressed in cancer encoding a novel protein with four K-homologous (KH) domains. KH-domains are found in a subset of RNA-binding proteins, including pre-mRNA-binding (hnRNP) K protein and the fragile X mental retardation gene product (FMR1). By fluorescence in situ hybridization (FISH) the identified gene named koc (KH domain containing protein overexpressed in cancer) was assigned to chromosome 7p11.5. Two pseudogenes were localised on chromosome 6 and 11. The cloned koc cDNA has a 250 bp 5'-UTR, a 1740 bp ORF and a 2168 bp 3'-UTR. The AU-rich 3'-untranslated region of koc contains eight AUUUA and four AUUUUUA reiterated motifs. The deduced koc protein with 580 amino-acids has a relative molecular mass (Mr) of approximately 65,000 (65 K). The koc transcript is highly overexpressed in pancreatic cancer cell lines and in pancreatic cancer tissue as compared to both, normal pancreas and chronic pancreatitis tissue. High levels of expression were as well found in tissue samples of other human tumours. As the KH domain has been shown to be involved in the regulation of RNA synthesis and metabolism, we speculate that koc may assume a role in the regulation of tumour cell proliferation by interfering with transcriptional and or posttranscriptional processes. However, the precise role of koc in human tumour cells is unknown and remains to be elucidated.

MeSH Terms
Amino Acid Sequence Base Sequence Cloning, Molecular DNA, Complementary Humans In Situ Hybridization, Fluorescence Molecular Sequence Data Neoplasm Proteins Pancreatic Neoplasms/genetics RNA, Messenger/genetics,metabolism RNA-Binding Proteins/genetics Sequence Homology, Amino Acid Tumor Cells, Cultured
Chemicals
DNA, Complementary IGF2BP3 protein, human Neoplasm Proteins RNA, Messenger RNA-Binding Proteins
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Müeller-Pillasch F
Department of Internal Medicine I, University of Ulm, Germany.
Lacher U
Wallrapp C
Micha A
Zimmerhackl F
Hameister H
Varga G
Friess H
Büchler M
Beger H G
Vila M R
Adler G
Gress T M
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1997-06-05
Pages
2729-33
Language
English
Region
England
NLM ID
8711562
Subset
IM
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