cDNA microarray in isolation of novel differentially expressed genes related to human glioma and clone of a novel full-length gene.
- Author:
Zhen-yu QI
1
;
Guo-zhen HUI
;
Yao LI
;
Zong-xiang ZHOU
;
Shao-hua GU
;
Kang YING
;
Yi XIE
Author Information
- Publication Type:Journal Article
- MeSH: Amino Acid Sequence; Base Sequence; Blotting, Northern; Cyclophilins; genetics; Cyclosporine; pharmacology; Glioma; genetics; Humans; Molecular Sequence Data; Oligonucleotide Array Sequence Analysis; RNA, Messenger; analysis
- From: Chinese Medical Journal 2005;118(10):799-805
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDThis investigation was undertaken to obtain differentially expressed genes related to human glioma using cDNA microarray and the characterization of one novel full-length gene.
METHODSTotal RNA was extracted from human glioma tissues and normal brain tissues, and mRNA was used to make probes. After hybridization and washing, the results were scanned using a computer system. The gene named 681F05 clone was an expressed gene to human glioma through four-time hybridization and scanning. Subsequently northern blot analysis was performed by northern blot, 5'RACE and bioinformatics.
RESULTSFifteen differentially expressed genes to human glioma were obtained through four-time hybridization and scanning. Northern blot analysis confirmed that 681F05 clone was low-expressed in human brain tissues and over-expressed in human glioma tissues. The analysis of BLASTn and BLASTx showed that 681F05 clone is two cDNA clones encoding two novel proteins that are highly identified to the cyclophilin isoform 10 of C. Elgans, respectively. Sequence analysis revealed the two cDNA clones are two different splicing variants of a novel cycophilin-like gene (PPIL3a and PPIL3b).
CONCLUSIONScDNA microarray technology can be successfully used to identify differentially expressed genes. The novel full-length gene of human PPIL3 may be correlated with the formation of human glioma.