Literature DB >> 10772858

Protein-protein interaction among hnRNPs shuttling between nucleus and cytoplasm.

J H Kim1, B Hahm, Y K Kim, M Choi, S K Jang.   

Abstract

Heterogeneous nuclear ribonucleoproteins (hnRNPs) are involved in several RNA-related biological processes such as transcription, pre-mRNA processing, mature mRNA transport to the cytoplasm, and translation. About 20 major hnRNPs from A1 to U are known. Among them, hnRNP A, D, E, I, and K are known to shuttle between the nucleus and the cytoplasm. hnRNP E2 has been seen to stabilize alpha-globin mRNA and to enhance polioviral mRNA translation. hnRNP K modulates transcription and translation of some mRNAs. hnRNP I and its homologue hnRNP L have been suggested to enhance translation of some IRES-dependent mRNAs. In order to better understand the molecular mechanisms of the biological functions of hnRNPs, we investigated protein-protein interactions of six hnRNPs (hnRNP A1, C1, E2, I, K, and L) using the yeast two-hybrid system and in vitro co-precipitation assays. All of the hnRNPs tested exerted homomeric interactions, and hnRNP E2, I, K, and L interacted with each other. In the case of hnRNP E2 and hnRNP K, the N-terminal half of the proteins containing two KH (K homologous) domains were required for protein-protein interaction, and the second quarter of hnRNP I and hnRNP L containing RRM2 (RNA recognition motif 2) was essential for protein-protein interaction. hnRNP A1 and C1 did not form complexes with other hnRNPs in our assay systems. This suggests that the hnRNPs could fall into two groups: one group, including hnRNP A1 and C1, involved in hnRNP core complex formation and another group, including hnRNP E2, I, K, and L, involved in a variety of RNA-related biological processes. Different combinations of the proteins of the second group may facilitate different biological processes in conjunction with other factors. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10772858     DOI: 10.1006/jmbi.2000.3687

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  76 in total

1.  Translation of polioviral mRNA is inhibited by cleavage of polypyrimidine tract-binding proteins executed by polioviral 3C(pro).

Authors:  Sung Hoon Back; Yoon Ki Kim; Woo Jae Kim; Sungchan Cho; Hoe Rang Oh; Jung-Eun Kim; Sung Key Jang
Journal:  J Virol       Date:  2002-03       Impact factor: 5.103

2.  The KH domains of Xenopus Vg1RBP mediate RNA binding and self-association.

Authors:  Anna Git; Nancy Standart
Journal:  RNA       Date:  2002-10       Impact factor: 4.942

3.  Poly(C)-binding protein 2 interacts with sequences required for viral replication in the hepatitis C virus (HCV) 5' untranslated region and directs HCV RNA replication through circularizing the viral genome.

Authors:  Linya Wang; King-Song Jeng; Michael M C Lai
Journal:  J Virol       Date:  2011-06-01       Impact factor: 5.103

4.  Identification of cellular proteins enhancing activities of internal ribosomal entry sites by competition with oligodeoxynucleotides.

Authors:  Kobong Choi; Jong Heon Kim; Xiaoyu Li; Ki Young Paek; Sang Hoon Ha; Sung Ho Ryu; Eckard Wimmer; Sung Key Jang
Journal:  Nucleic Acids Res       Date:  2004-02-23       Impact factor: 16.971

Review 5.  Diverse regulation of 3' splice site usage.

Authors:  Muhammad Sohail; Jiuyong Xie
Journal:  Cell Mol Life Sci       Date:  2015-09-14       Impact factor: 9.261

6.  Binding of hnRNP L to the pre-mRNA processing enhancer of the herpes simplex virus thymidine kinase gene enhances both polyadenylation and nucleocytoplasmic export of intronless mRNAs.

Authors:  Shouhong Guang; Alicia M Felthauser; Janet E Mertz
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

7.  Heterogeneous nuclear ribonucleoprotein (hnRNP) E1 binds to hnRNP A2 and inhibits translation of A2 response element mRNAs.

Authors:  Linda D Kosturko; Michael J Maggipinto; George Korza; Joo Won Lee; John H Carson; Elisa Barbarese
Journal:  Mol Biol Cell       Date:  2006-06-14       Impact factor: 4.138

8.  A nucleo-cytoplasmic SR protein functions in viral IRES-mediated translation initiation.

Authors:  Kristin M Bedard; Sarah Daijogo; Bert L Semler
Journal:  EMBO J       Date:  2006-12-21       Impact factor: 11.598

9.  BiP internal ribosomal entry site activity is controlled by heat-induced interaction of NSAP1.

Authors:  Sungchan Cho; Sung Mi Park; Tae Don Kim; Jong Heon Kim; Kyong-Tai Kim; Sung Key Jang
Journal:  Mol Cell Biol       Date:  2006-10-30       Impact factor: 4.272

10.  The sld genetic defect: two intronic CA repeats promote insertion of the subsequent intron and mRNA decay.

Authors:  Biswadip Das; Melanie N Cash; Bently Robinson; Christopher S Kuhns; Lisa R Latchney; Margaret A Fallon; Rosemary W Elliott; Arthur R Hand; David J Culp
Journal:  J Biol Chem       Date:  2013-04-11       Impact factor: 5.157

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