Literature DB >> 9447706

Evidence that "pinin", reportedly a differentiation-specific desmosomal protein, is actually a widespread nuclear protein.

J M Brandner1, S Reidenbach, W W Franke.   

Abstract

A protein recently described as a desmosome-specific molecule involved in anchoring intermediate-sized filaments (IFs) to the desmosomal plaque, and hence named "pinin" [43], has been known in our laboratory for several years as a strictly nuclear protein occurring in a wide range of cell types, including many that are totally devoid of desmosomes. Using a series of specific antibodies we have localized the protein in the nucleoplasm of cultured cells, blood cells and solid tissues of diverse vertebrate species, from oocytes to erythrocytes of amphibia and from liver to connective tissue and fibroblasts in mammals. Desmosomes have consistently been negative, and the nuclear specificity of the immunolocalization reactions has also been directly demonstrated by double-label immunofluorescence microscopy. From our results we conclude that this nuclear protein, characterized by a domain exceptionally rich in serine residues and hence termed DRS-protein, occurs in at least two genetically different forms in a diffusible state as well as in special ribonucleoprotein-particles, "speckles" [6], and is a widespread if not ubiquitous nuclear protein. Consequently it must serve nuclear functions rather than "pinning" IFs to plasma membranes and does not provide a new reliable marker for desmosomes and epithelial or myocardial differentiation.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9447706     DOI: 10.1046/j.1432-0436.1997.6230119.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  14 in total

1.  The alpha isoform of protein kinase C is involved in signaling the response of desmosomes to wounding in cultured epithelial cells.

Authors:  S Wallis; S Lloyd; I Wise; G Ireland; T P Fleming; D Garrod
Journal:  Mol Biol Cell       Date:  2000-03       Impact factor: 4.138

2.  Identification of a sequence element directing a protein to nuclear speckles.

Authors:  J Eilbracht; M S Schmidt-Zachmann
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

3.  Proteomic analysis of interchromatin granule clusters.

Authors:  Noriko Saitoh; Chris S Spahr; Scott D Patterson; Paula Bubulya; Andrew F Neuwald; David L Spector
Journal:  Mol Biol Cell       Date:  2004-05-28       Impact factor: 4.138

Review 4.  Cell-context dependent TCF/LEF expression and function: alternative tales of repression, de-repression and activation potentials.

Authors:  Catherine D Mao; Stephen W Byers
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2011       Impact factor: 1.807

Review 5.  Recent progress in histochemistry and cell biology.

Authors:  Stefan Hübner; Athina Efthymiadis
Journal:  Histochem Cell Biol       Date:  2012-02-25       Impact factor: 4.304

6.  Dissection of the role of Pinin in the development of zebrafish posterior pharyngeal cartilages.

Authors:  Shu-Yuan Hsu; Yi-Chuan Cheng; Hung-Yu Shih; Pin Ouyang
Journal:  Histochem Cell Biol       Date:  2012-04-20       Impact factor: 4.304

7.  Pnn and SR family proteins are differentially expressed in mouse central nervous system.

Authors:  Shu-Yuan Hsu; Yen-Jung Chen; Pin Ouyang
Journal:  Histochem Cell Biol       Date:  2011-03-10       Impact factor: 4.304

8.  Nuclear Pnn/DRS protein binds to spliced mRNPs and participates in mRNA processing and export via interaction with RNPS1.

Authors:  Chin Li; Ru-Inn Lin; Ming-Chih Lai; Pin Ouyang; Woan-Yuh Tarn
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

9.  Human RNPS1 and its associated factors: a versatile alternative pre-mRNA splicing regulator in vivo.

Authors:  Eiji Sakashita; Sawako Tatsumi; Dieter Werner; Hitoshi Endo; Akila Mayeda
Journal:  Mol Cell Biol       Date:  2004-02       Impact factor: 4.272

10.  Nuclear speckle-associated protein Pnn/DRS binds to the transcriptional corepressor CtBP and relieves CtBP-mediated repression of the E-cadherin gene.

Authors:  Roman Alpatov; Gustavo Costa Munguba; Paul Caton; Jeong Hoon Joo; Yang Shi; Yujiang Shi; Marguerite E Hunt; Stephen P Sugrue
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.