Literature DB >> 24569877

Fam118B, a newly identified component of Cajal bodies, is required for Cajal body formation, snRNP biogenesis and cell viability.

Yujing Li1, Ka-Wing Fong, Mengfan Tang, Xin Han, Zihua Gong, Wenbin Ma, Michael Hebert, Zhou Songyang, Junjie Chen.   

Abstract

Cajal bodies are specialized and dynamic compartments in the nucleus that are involved in the biogenesis of small nuclear ribonucleoproteins (snRNPs). Because of the dynamic and varied roles of Cajal bodies, it is of great interest to identify the components of Cajal bodies to better understand their functions. We performed a genome-wide screen to identify proteins that colocalize with coilin, the marker protein of Cajal bodies. In this study, we identified and characterized Fam118B as a newly discovered component of Cajal bodies. Fam118B is widely expressed in a variety of cell lines derived from various origins. Overexpression of Fam118B changes the canonical morphology of Cajal bodies, whereas depletion of Fam118B disrupts the localization of components of Cajal bodies, including coilin, the survival of motor neuron protein (SMN) and the Sm protein D1 (SmD1, also known as SNRPD1). Moreover, depletion of Fam118B reduces splicing capacity and inhibits cell proliferation. In addition, Fam118B associates with coilin and SMN proteins. Fam118B depletion reduces symmetric dimethylarginine modification of SmD1, which in turn diminishes the binding of SMN to this Sm protein. Taken together, these data indicate that Fam118B, by regulating SmD1 symmetric dimethylarginine modification, plays an important role in Cajal body formation, snRNP biogenesis and cell viability.

Entities:  

Keywords:  Cajal body; Coilin; Fam118B; SMN; Symmetric dimethylarginine

Mesh:

Substances:

Year:  2014        PMID: 24569877      PMCID: PMC4004977          DOI: 10.1242/jcs.143453

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  42 in total

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Authors:  M D Hebert; A G Matera
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3.  The C-terminal RG dipeptide repeats of the spliceosomal Sm proteins D1 and D3 contain symmetrical dimethylarginines, which form a major B-cell epitope for anti-Sm autoantibodies.

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Review 5.  Phosphorylation and the Cajal body: modification in search of function.

Authors:  Michael D Hebert
Journal:  Arch Biochem Biophys       Date:  2010-03-01       Impact factor: 4.013

6.  SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets.

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Journal:  Mol Cell       Date:  2001-05       Impact factor: 17.970

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9.  Residual Cajal bodies in coilin knockout mice fail to recruit Sm snRNPs and SMN, the spinal muscular atrophy gene product.

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Journal:  J Cell Biol       Date:  2001-07-23       Impact factor: 10.539

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Authors:  Michael P Walker; Liping Tian; A Gregory Matera
Journal:  PLoS One       Date:  2009-07-09       Impact factor: 3.240

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9.  Nuclear bodies formed by polyQ-ataxin-1 protein are liquid RNA/protein droplets with tunable dynamics.

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10.  The Insertion in Fingers Domain in Human Telomerase Can Mediate Enzyme Processivity and Telomerase Recruitment to Telomeres in a TPP1-Dependent Manner.

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