Literature DB >> 10198427

Npw38, a novel nuclear protein possessing a WW domain capable of activating basal transcription.

A Komuro1, M Saeki, S Kato.   

Abstract

We have found a novel cDNA encoding a 265 amino acid protein possessing a WW domain in our full-length cDNA bank. The WW domain was sandwiched between an acidic region and an acidic-basic amino acid repetitive region. In vitro transcription/translation of the cDNA produced a 38 kDa product that was also found in the cell lysate by western blot analysis. Thus this protein is named the nuclear protein containing a WW domain with a molecular mass of 38 kDa, Npw38. Immunofluorescence studies and expression of a fusion protein to a green fluorescent protein revealed that this protein is localized in the nucleus. Npw38 was shown to be capable of binding to a poly(rG) resin. Interestingly, the WW domain of Npw38 was found to function as a transcriptional activator in CHO cells using the GAL4 DNA-binding fusion system. Furthermore, the WW domains of human YAP and Pin1 were demonstrated to have a similar transcription-promoting activity. Combined mutation of the conserved first and second Trp residues and a hydrophobic triplet of TyrTyrTrp in the WW domain of Npw38 abolished the transcription-promoting activity, but single mutations of these sites did not. These results suggest that some WW domains potentially possess transcription-promoting activity in mammalian cells.

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Year:  1999        PMID: 10198427      PMCID: PMC148407          DOI: 10.1093/nar/27.9.1957

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  11 in total

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Authors:  X Wu; C B Wilcox; G Devasahayam; R L Hackett; M Arévalo-Rodríguez; M E Cardenas; J Heitman; S D Hanes
Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

4.  Candidate genes in quantitative trait loci associated with absolute and relative kidney weight in rats with Inherited Stress Induced Arterial Hypertension.

Authors:  Olga E Redina; Svetlana E Smolenskaya; Leonid O Klimov; Arcady L Markel
Journal:  BMC Genet       Date:  2015-02-02       Impact factor: 2.797

5.  Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene.

Authors:  H Lubs; F E Abidi; R Echeverri; L Holloway; A Meindl; R E Stevenson; C E Schwartz
Journal:  J Med Genet       Date:  2006-06       Impact factor: 6.318

6.  Y65C missense mutation in the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1 affects its binding activity and deregulates pre-mRNA splicing.

Authors:  Victor E Tapia; Emilia Nicolaescu; Caleb B McDonald; Valeria Musi; Tsutomu Oka; Yujin Inayoshi; Adam C Satteson; Virginia Mazack; Jasper Humbert; Christian J Gaffney; Monique Beullens; Charles E Schwartz; Christiane Landgraf; Rudolf Volkmer; Annalisa Pastore; Amjad Farooq; Mathieu Bollen; Marius Sudol
Journal:  J Biol Chem       Date:  2010-04-21       Impact factor: 5.157

7.  The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling.

Authors:  Yasuno Iwasaki; Gerald H Thomsen
Journal:  Development       Date:  2014-09-10       Impact factor: 6.868

8.  The Renpenning syndrome-associated protein PQBP1 facilitates the nuclear import of splicing factor TXNL4A through the karyopherin β2 receptor.

Authors:  Xian Liu; Lin-Xia Dou; Junhai Han; Zi Chao Zhang
Journal:  J Biol Chem       Date:  2020-02-10       Impact factor: 5.157

9.  Bio-molecular architects: a scaffold provided by the C-terminal domain of eukaryotic RNA polymerase II.

Authors:  Mengmeng Zhang; Gordon N Gill; Yan Zhang
Journal:  Nano Rev       Date:  2010-08-30

10.  Subnuclear compartmentalization of transiently expressed polyadenylated pri-microRNAs: processing at transcription sites or accumulation in SC35 foci.

Authors:  Jan M Pawlicki; Joan A Steitz
Journal:  Cell Cycle       Date:  2009-02-21       Impact factor: 4.534

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