Identification of a novel isoform of DHRS4 protein with a nuclear localization signal

被引:5
|
作者
Su, Zhongjing [1 ]
Li, Rui [1 ]
Song, Xuhong [1 ]
Liu, Gefei [1 ]
Li, Yifan [1 ]
Chang, Xiaolan [1 ]
Li, Congzhu [2 ]
Huang, Dongyang [1 ]
机构
[1] Shantou Univ, Coll Med, Dept Cell Biol, Shantou Guangdong 515041, Peoples R China
[2] Shantou Univ, Coll Med, Canc Hosp, Shantou Guangdong 515041, Peoples R China
基金
中国国家自然科学基金;
关键词
Alternative splicing; Nuclear localization signal; DHRS4; gene; NADP(H)-dependent retinol dehydrogenase/reductase; SHORT-CHAIN DEHYDROGENASE/REDUCTASE; MESSENGER-RNA DECAY; TETRAMERIC CARBONYL REDUCTASE; TARGETING SEQUENCE; GENE-CLUSTER; EXPRESSION; LIVER; MITOCHONDRIA; MECHANISMS; IMPORT;
D O I
10.1016/j.gene.2011.12.033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The DHRS4 gene encodes an NADP(H)-dependent retinol dehydrogenase/reductase (NRDR) and plays an important role in regulating the synthesis of retinoic acid. In the present study, we identified a novel splice RNA variant, designated NRDRA2, of the human DHRS4 gene by RT-PCR, 3' RACE, and 5' RACE. NRDRA2 mRNA lacked exons 4 and 6, and had a shift in the reading frame when compared to DHRS4 mRNA, resulting in loss of the peroxisomal targeting signal of NRDR and gain of a nuclear localization signal in the predicted NRDRA2 protein. Endogenous NRDRA2 protein was identified in the human cervical carcinoma cell line HeLa by immunoprecipitation and mass spectrometric assay. A green fluorescent protein reporter assay showed that NRDRA2 protein mainly localized to the nuclei, confirming the sequence at its C-terminus as a legitimate nuclear localization signal sequence. This study identifies the alternative transcript variant NRDRA2 encoding a subcellular nuclear localized NRDRA2 protein. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 167
页数:7
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