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PMID: 15126345 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma.

Cancer research ·Vol. 64 ·No. 9 ·2004-05-01 ·Pages 3087-95

Ota A, Tagawa H, Karnan S, Tsuzuki S, Karpas A, Kira S, Yoshida Y, Seto M

Abstract

The amplification at 13q31-q32 has been reported in not only hematopoietic malignancies but also in other solid tumors. We identified previously frequent amplification of chromosomal band 13q31-q32 in 70 cases of diffuse large B-cell lymphoma patients by conventional comparative genomic hybridization analysis. In an attempt to identify a candidate gene within this region, we used array comparative genomic hybridization and fluorescent in situ hybridization to map the 13q31-q32 amplicon. We then screened the 65 expressed sequence tags and Glypican 5 (GPC5) by reverse transcription-PCR and Northern blotting. As a result, we identified a novel gene, designated Chromosome 13 open reading frame 25 (C13orf25), which was overexpressed in B-cell lymphoma cell lines and diffuse large B-cell lymphoma patients with 13q31-q32 amplifications. However, GPC5, which has been reported to be a target gene for 13q31-q32 amplification, was truncated in one cell line, Rec1, possessing the amplification, and its expression in various cell lines with amplification at 13q31-q32 was not significantly different from that in other cell lines without amplification, suggesting that GPC5 is not likely to be the candidate gene. Additional analysis identified two major transcripts in the C13orf25 gene. The two transcripts A and B predicted open reading frames of 32 and 70-amino acid polypeptides, respectively. The former has been reported as bA121J7.2, which is conserved among species. Transcript-B also contained seven mature microRNAs in its untranslated region. These results suggest that the C13orf25 gene is the most likely candidate gene for the 13q31-q32 amplicon found in hematopoietic malignancies.

MeSH Terms
Amino Acid Sequence Blotting, Northern Cell Line, Tumor Chromosomes, Human, Pair 13/genetics Extracellular Matrix Proteins Gene Amplification Glypicans Heparan Sulfate Proteoglycans/genetics Humans Lymphoma, B-Cell/genetics Lymphoma, Large B-Cell, Diffuse/genetics Molecular Sequence Data Nucleic Acid Hybridization Open Reading Frames/genetics Reverse Transcriptase Polymerase Chain Reaction
Chemicals
Extracellular Matrix Proteins GPC5 protein, human Glypicans Heparan Sulfate Proteoglycans
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Ota Akinobu
Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.
Tagawa Hiroyuki
Karnan Sivasundaram
Tsuzuki Shinobu
Karpas Abraham
Kira Shigeki
Yoshida Yasuko
Seto Masao
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2004-05-01
Pages
3087-95
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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