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cAMP-Dependent Posttranscriptional Regulation of Steroidogenic Acute Regulatory (STAR) Protein by the Zinc Finger Protein ZFP36L1/TIS11b

Duan, Haichuan, Cherradi, Nadia, Feige, Jean-Jacques, Jefcoate, Colin·2009·Molecular Endocrinology
DOI 10.1210/me.2008-0296
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Abstract

Star is expressed in steroidogenic cells as 3.5- and 1.6-kb transcripts that differ only in their 3′-untranslated regions (3′-UTR). In mouse MA10 testis and Y-1 adrenal lines, Br-cAMP preferentially stimulates 3.5-kb mRNA. ACTH is similarly selective in primary bovine adrenocortical cells. The 3.5-kb form harbors AU-rich elements (AURE) in the extended 3′-UTR, which enhance turnover. After peak stimulation of 3.5-kb mRNA, degradation is seen. Star mRNA turnover is enhanced by the zinc finger protein ZFP36L1/TIS11b, which binds to UAUUUAUU repeats in the extended 3′-UTR. TIS11b is rapidly stimulated in each cell type in parallel with Star mRNA. Cotransfection of TIS11b selectively decreases cytomegalovirus-promoted Star mRNA and luciferase-Star 3′-UTR reporters harboring the extended 3′-UTR. Direct complex formation was demonstrated between TIS11b and the extended 3′-UTR of the 3.5-kb Star. AURE mutations revealed that TIS11b-mediated destabilization required the first two UAUUUAUU motifs. HuR, which also binds AURE, did not affect Star expression. Targeted small interfering RNA knockdown of TIS11b specifically enhanced stimulation of 3.5-kb Star mRNA in bovine adrenocortical cells, MA-10, and Y-1 cells but did not affect the reversals seen after peak stimulation. Direct transfection of Star mRNA demonstrated that Br-cAMP stimulated a selective turnover of 3.5-kb mRNA independent of AURE, which may correspond to these reversal processes. Steroidogenic acute regulatory (STAR) protein induction was halved by TIS11b knockdown, concomitant with decreased cholesterol metabolism. TIS11b suppression of 3.5-kb mRNA is therefore surprisingly coupled to enhanced Star translation leading to increased cholesterol metabolism.

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  • ZFP36 family members interact with AREs containing a UAUUUAUU sequence and trigger degradation of several ARE-containing mRNAs, including PLK3 and VEGFA.

    “ZFP36L1 and ZFP36L2 belong to the family of CCCH tandem zinc finger proteins (the ZFP36 family), members of which interact with AREs containing a UAUUUAUU sequence and trigger the degradation of several ARE-containing mRNAs, including PLK3 and VEGFA (7,8,18,19).”

    From ZFP36L1 and ZFP36L2 control LDLR mRNA stability via the ERK–RSK pathway (2014) · cites this paper as [19]

    The paper's background section says that ZFP36-family proteins bind AU-rich elements and promote mRNA degradation, and identifies UAUUUAUU as a binding sequence. It also reports TIS11b-mediated destabilization of VEGF mRNA. Our copy does not identify PLK3 as a target (searched: PLK3, polo-like kinase 3). Page numbers were not available in the indexed passages. (LLM, conf=0.88)

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Metadata

Authors
Duan, H., Cherradi, N., Feige, J.-J., & Jefcoate, C.
Affiliations
  • Molecular and Cellular Pharmacology Graduate Program (H.D.), Madison, Wisconsin 53706
  • Institut National de la Santé et de la Recherche Médicale (N.C., J.-J.F.), Unité 878
  • University of Wisconsin-Madison, and Department of Pharmacology (C.J.), University of Wisconsin-Madison Medical School, Madison, Wisconsin 53706
Venue
Molecular Endocrinology
Publisher
The Endocrine Society
Published
2009-04-01
Volume
23
Issue
4
Pages
497-509
ISSN
  • 0888-8809
  • 1944-9917
DOI
10.1210/me.2008-0296
Cited by
42
References
6
Language
en

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