Comparative expression of tristetraprolin (TTP) family member transcripts in normal human tissues and cancer cell lines

被引:68
作者
Carrick, Danielle M.
Blackshear, Perry J.
机构
[1] NIEHS, Off Clin Res, Res Triangle Pk, NC 27709 USA
[2] NIEHS, Neurobiol Lab, Res Triangle Pk, NC 27709 USA
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
关键词
AU-rich element; tandem zinc finger proteins; mRNA turnover; deadenylation;
D O I
10.1016/j.abb.2007.04.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The tristetraprolin (TTP) family of tandem zinc finger proteins comprises three members in man and most other mammals, with a fourth expressed in rodents. In mice, gene disruption of TTP itself leads to a systemic inflammatory syndrome that is mediated in large part by over-expression of tumor necrosis factor alpha (TNF). This increased expression is secondary to stabilization of the TNF mRNA in the TTP KO mice, a finding that led to the characterization of TTP as an mRNA binding protein that can promote the removal of the poly(A) tail from selected mRNAs and facilitate their nucleolytic destruction. The other human family members behave similarly to TTP in over-expression studies of transfected cells, but gene disruption experiments have implicated them in different physiological processes. In the present study, we developed a real-time PCR assay for all three human family members that allowed for comparative measurements of all three family members in the same tissues and cells. We used this assay to quantitate expression levels of all three transcripts in a variety of normal human tissues, as well as in the "NCI 60", a well characterized panel of human tumor cell lines. Although studies in fibroblasts and macrophages derived from knockout mice have failed to demonstrate compensatory expression of the family members in terms of transcript levels, it remains possible that the different family members can function as "TTP equivalents" in certain physiological or pathological circumstances. (C) 2007 Published by Elsevier Inc.
引用
收藏
页码:278 / 285
页数:8
相关论文
共 31 条
[1]   Tristetraprolin and other CCCH tandem zinc-finger proteins in the regulation of mRNA turnover [J].
Blackshear, PJ .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2002, 30 :945-952
[2]   Zfp36l3, a rodent X chromosome gene encoding a placenta-specific member of the tristetraprolin family of CCCH tandem zinc finger proteins [J].
Blackshear, PJ ;
Phillips, RS ;
Ghosh, S ;
Ramos, SVB ;
Richfield, EK ;
Lai, WS .
BIOLOGY OF REPRODUCTION, 2005, 73 (02) :297-307
[3]   RNA sequence elements required for high affinity binding by the zinc finger domain of tristetraprolin - Conformational changes coupled to the bipartite nature of AU-rich mRNA-destabilizing motifs [J].
Brewer, BY ;
Malicka, J ;
Blackshear, PJ ;
Wilson, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (27) :27870-27877
[4]   Immunological characterization of tristetraprolin as a low abundance, inducible, stable cytosolic protein [J].
Cao, HP ;
Tuttle, JS ;
Blackshear, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :21489-21499
[5]   Bone marrow transplantation reproduces the tristetraprolin-deficiency syndrome in recombination activating gene-2 (-/-) mice - Evidence that monocyte/macrophage progenitors may be responsible for TNF alpha overproduction [J].
Carballo, E ;
Gilkeson, GS ;
Blackshear, PJ .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :986-995
[6]   Feedback inhibition of macrophage tumor necrosis factor-α production by tristetraprolin [J].
Carballo, E ;
Lai, WS ;
Blackshear, PJ .
SCIENCE, 1998, 281 (5379) :1001-1005
[7]   Roles of tumor necrosis factor-α receptor subtypes in the pathogenesis of the tristetraprolin-deficiency syndrome [J].
Carballo, E ;
Blackshear, PJ .
BLOOD, 2001, 98 (08) :2389-2395
[8]   The tandem CCCH zinc finger protein tristetraprolin and its relevance to cytokine mRNA turnover and arthritis [J].
Carrick, DM ;
Lai, WS ;
Blackshear, PJ .
ARTHRITIS RESEARCH & THERAPY, 2004, 6 (06) :248-264
[9]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[10]  
DUBOIS RN, 1990, J BIOL CHEM, V265, P19185