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

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 wi...

Full description

Saved in:
Bibliographic Details
Published inJournal of human genetics Vol. 56; no. 9; pp. 676 - 681
Main Authors Peiró, Ana M, Tang, Chih-Min, Murray, Fiona, Zhang, Lingzhi, Brown, Loren M, Chou, Daisy, Rassenti, Laura, Kipps, Thomas A, Insel, Paul A
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2011
Nature Publishing Group
Subjects
Online AccessGet full text
ISSN1434-5161
1435-232X
1435-232X
DOI10.1038/jhg.2011.80

Cover

More Information
Summary: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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Feature-1
content type line 23
ISSN:1434-5161
1435-232X
1435-232X
DOI:10.1038/jhg.2011.80