Genetic variation in phosphodiesterase (PDE) 7B in chronic lymphocytic leukemia: overview of genetic variants of cyclic nucleotide PDEs in human disease

被引:7
作者
Peiro, Ana M. [1 ,2 ]
Tang, Chih-Min [1 ]
Murray, Fiona [1 ,3 ]
Zhang, Lingzhi [1 ]
Brown, Loren M. [1 ]
Chou, Daisy [1 ]
Rassenti, Laura [4 ]
Kipps, Thomas A. [3 ,4 ]
Insel, Paul A. [1 ,3 ,4 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Hosp Gen Univ Alicante, Dept Clin Pharmacol, Alicante, Spain
[3] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
关键词
cAMP; chronic lymphocytic leukemia; cyclic nucleotide phosphodiesterases; PDE7B single-nucleotide polymorphisms; COPY-NUMBER VARIATION; ISCHEMIC-STROKE; 4D GENE; CAMP-PHOSPHODIESTERASE; DOWN-REGULATION; 3B GENE; RISK; ASSOCIATION; POLYMORPHISMS; EXPRESSION;
D O I
10.1038/jhg.2011.80
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Expression of cyclic adenosine monophosphate-specific phosphodiesterase 7B (PDE7B) mRNA is increased in patients with chronic lymphocytic leukemia (CLL), thus suggesting that variation may occur in the PDE7B gene in CLL. As genetic variation in other PDE family members has been shown to associate with numerous clinical disorders (reviewed in this manuscript), we sought to identify single-nucleotide polymorphisms (SNPs) in the PDE7B gene promoter and coding region of 93 control subjects and 154 CLL patients. We found that the PDE7B gene has a 5' non-coding region SNP -347C>T that occurs with similar frequency in CLL patients (1.9%) and controls (2.7%). Tested in vitro, -347C>T has less promoter activity than a wild-type construct. The low frequency of this 5' untranslated region variant indicates that it does not explain the higher PDE7B expression in patients with CLL but it has the potential to influence other settings that involve a role for PDE7B. Journal of Human Genetics (2011) 56, 676-681; doi:10.1038/jhg.2011.80; published online 28 July 2011
引用
收藏
页码:676 / 681
页数:6
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