RNase-L Control of Cellular mRNAs: Roles in Biologic Functions and Mechanisms of Substrate Targeting-Reference-Cited by-同舟云学术

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RNase-L Control of Cellular mRNAs: Roles in Biologic Functions and Mechanisms of Substrate Targeting

Published:2014-04 Issue:4 Volume:34 Page:275-288
ISSN:1079-9907
Container-title:Journal of Interferon & Cytokine Research
language:en
Short-container-title:Journal of Interferon & Cytokine Research

Author:

Brennan-Laun Sarah E.¹²,Ezelle Heather J.¹²³,Li Xiao-Ling⁴,Hassel Bret A.¹²³

Affiliation:

1. Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland.

2. Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland.

3. Research Services, Baltimore Veterans Affairs Medical Center, Baltimore, Maryland.

4. Genetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Publisher

Mary Ann Liebert Inc

Subject

Virology,Cell Biology,Immunology

Link

http://www.liebertpub.com/doi/pdf/10.1089/jir.2013.0147

Reference127 articles.

1. RNase L downmodulation of the RNA-binding protein, HuR, and cellular growth

2. Regulation of p21/CIP1/WAF-1 mediated cell-cycle arrest by RNase L and tristetraprolin, and involvement of AU-rich elements

3. Structure of the Ire1 autophosphorylation complex and implications for the unfolded protein response

4. Ribosomal protein mRNAs are primary targets of regulation in RNase-L-induced senescence

5. &cestchinlong;Visibly stressed: the role of eIF2, TIA-1, and stress granules in protein translation

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