Literature DB >> 21189691

Reaching for the stars: Linking RNA binding proteins to diseases.

Stéphane Richard1.   

Abstract

The prototype STAR (Signal Transduction and Activation of RNA) protein is Sam68, the Src-associated substrate during mitosis of 68 kDa. Sam68, like all other STAR proteins, belongs to the large class of heteronuclear ribonucleoprotein particle K (hnRNP K) homology (KH) domain family of RNA-binding proteins. The KH domain is an evolutionarily conserved RNA binding domain that consists of 70-100 amino acids. The KH domain is one of the most prevalent RNA binding domains that directly contacts single-stranded RNA with a signature topology. Sam68 contains a single KH domain that harbors additional conserved N- and C-terminal sequences also required for RNA binding specificity and dimerization. Sam68 frequently contains post-translational modifications including serine/threonine, tyrosine phosphorylation, lysine acetylation, arginine methylation and sumoylation. The phosphorylation of Sam68 or its association with SH3 domain containing proteins has been shown to influence its RNA binding activity. Hence Sam68 behaves as a STAR protein, whereby extracellular signals influence its ability to regulate RNA metabolism. Studies in mice have revealed physiological roles linking Sam68 to osteoporosis, cancer, infertility and ataxia. The role of Sam68, a closely related family member quaking (QKI), the KH domain and their links with human disease will be discussed in the present chapter.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21189691

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  24 in total

Review 1.  Neurodegeneration the RNA way.

Authors:  Abigail J Renoux; Peter K Todd
Journal:  Prog Neurobiol       Date:  2011-11-03       Impact factor: 11.685

Review 2.  RNA protein interaction in neurons.

Authors:  Robert B Darnell
Journal:  Annu Rev Neurosci       Date:  2013-05-20       Impact factor: 12.449

Review 3.  Mitochondrial retrograde signaling at the crossroads of tumor bioenergetics, genetics and epigenetics.

Authors:  Manti Guha; Narayan G Avadhani
Journal:  Mitochondrion       Date:  2013-09-01       Impact factor: 4.160

4.  Inhibition of Sam68 triggers adipose tissue browning.

Authors:  Junlan Zhou; Min Cheng; Chan Boriboun; Mariam M Ardehali; Changfei Jiang; Qinghua Liu; Shuling Han; David A Goukassian; Yao-Liang Tang; Ting C Zhao; Ming Zhao; Lu Cai; Stéphane Richard; Raj Kishore; Gangjian Qin
Journal:  J Endocrinol       Date:  2015-05-01       Impact factor: 4.286

5.  Hsp22 (HspB8/H11) knockdown induces Sam68 expression and stimulates proliferation of glioblastoma cells.

Authors:  Suhasini Modem; Kannagi Chinnakannu; Uma Bai; G Prem-Veer Reddy; Thipparthi R Reddy
Journal:  J Cell Physiol       Date:  2011-11       Impact factor: 6.384

6.  Phosphoproteomics Analysis Identifies Novel Candidate Substrates of the Nonreceptor Tyrosine Kinase, Src-related Kinase Lacking C-terminal Regulatory Tyrosine and N-terminal Myristoylation Sites (SRMS).

Authors:  Raghuveera Kumar Goel; Marta Paczkowska; Jüri Reimand; Scott Napper; Kiven Erique Lukong
Journal:  Mol Cell Proteomics       Date:  2018-03-01       Impact factor: 5.911

Review 7.  Emerging roles for Sam68 in adipogenesis and neuronal development.

Authors:  Gillian Vogel; Stéphane Richard
Journal:  RNA Biol       Date:  2012-09-01       Impact factor: 4.652

8.  Evolutionary Dynamics of GLD-1-mRNA complexes in Caenorhabditis nematodes.

Authors:  Alana V Beadell; Eric S Haag
Journal:  Genome Biol Evol       Date:  2014-12-09       Impact factor: 3.416

9.  Sam68 Regulates S6K1 Alternative Splicing during Adipogenesis.

Authors:  Jingwen Song; Stéphane Richard
Journal:  Mol Cell Biol       Date:  2015-03-16       Impact factor: 4.272

Review 10.  Context-specific protein tyrosine kinase 6 (PTK6) signalling in prostate cancer.

Authors:  Yu Zheng; Angela L Tyner
Journal:  Eur J Clin Invest       Date:  2013-02-10       Impact factor: 4.686

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.