Literature DB >> 10713668

Krp1, a novel kelch related protein that is involved in pseudopod elongation in transformed cells.

H J Spence1, I Johnston, K Ewart, S J Buchanan, U Fitzgerald, B W Ozanne.   

Abstract

We have previously shown that the transcription factor AP-1 regulates the expression of genes which allow neoplastically transformed rat fibroblasts to become invasive. Searches for further AP-1 target genes led to the identification of a gene encoding a novel rat kelch family member, named kelch related protein 1 (Krp1). Kelch family members are characterized by a series of repeats at their carboxyl terminus and a BTB/POZ domain near their amino terminus. Rat Krp1 has a primarily cytoplasmic localization, and a small fraction appears to accumulate and co-localize with F-actin at membrane ruffle-like structures in the tips of pseudopodia. Overexpression of Krp1 in transformed rat fibroblasts led to the formation of dramatically elongated pseudopodia, while expression of truncated Krp1 polypeptides resulted in a reduction in the length of pseudopodia. We propose that the transformation-specific expression of Krp1 is required for pseudopod elongation, which are structures that are required for cell motility and invasion.

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Year:  2000        PMID: 10713668     DOI: 10.1038/sj.onc.1203433

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  21 in total

1.  Keap1 is a redox-regulated substrate adaptor protein for a Cul3-dependent ubiquitin ligase complex.

Authors:  Donna D Zhang; Shih-Ching Lo; Janet V Cross; Dennis J Templeton; Mark Hannink
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

2.  Critical regulation of genes for tumor cell migration by AP-1.

Authors:  El Mustapha Bahassi; Saikumar Karyala; Craig R Tomlinson; Maureen A Sartor; Mario Medvedovic; Robert F Hennigan
Journal:  Clin Exp Metastasis       Date:  2004       Impact factor: 5.150

3.  AP-1 differentially expressed proteins Krp1 and fibronectin cooperatively enhance Rho-ROCK-independent mesenchymal invasion by altering the function, localization, and activity of nondifferentially expressed proteins.

Authors:  Heather J Spence; Lynn McGarry; Catherine S Chew; Neil O Carragher; Linda A Scott-Carragher; Zhengqiang Yuan; Daniel R Croft; Michael F Olson; Margaret Frame; Bradford W Ozanne
Journal:  Mol Cell Biol       Date:  2006-02       Impact factor: 4.272

4.  Krp1 (Sarcosin) promotes lateral fusion of myofibril assembly intermediates in cultured mouse cardiomyocytes.

Authors:  Cynthia C Greenberg; Patricia S Connelly; Mathew P Daniels; Robert Horowits
Journal:  Exp Cell Res       Date:  2008-03-10       Impact factor: 3.905

5.  EPS8 upregulates FOXM1 expression, enhancing cell growth and motility.

Authors:  Huixin Wang; Muy-Teck Teh; Youngmi Ji; Vyomesh Patel; Shahrzad Firouzabadian; Anisha A Patel; J Silvio Gutkind; W Andrew Yeudall
Journal:  Carcinogenesis       Date:  2010-03-29       Impact factor: 4.944

6.  BTB-Kelch protein Krp1 regulates proliferation and differentiation of myoblasts.

Authors:  Camille W Paxton; Ruth A Cosgrove; Anja C Drozd; Emma L Wiggins; Sam Woodhouse; Rachel A Watson; Heather J Spence; Brad W Ozanne; Jennifer M Pell
Journal:  Am J Physiol Cell Physiol       Date:  2011-03-02       Impact factor: 4.249

7.  Scaffolds and chaperones in myofibril assembly: putting the striations in striated muscle.

Authors:  Garland L Crawford; Robert Horowits
Journal:  Biophys Rev       Date:  2011-03-01

8.  Expression of peroxiredoxin 1 and 4 promotes human lung cancer malignancy.

Authors:  Hong Jiang; Lisha Wu; Murli Mishra; Hedy A Chawsheen; Qiou Wei
Journal:  Am J Cancer Res       Date:  2014-09-06       Impact factor: 6.166

9.  Dysregulation of NRAP degradation by KLHL41 contributes to pathophysiology in nemaline myopathy.

Authors:  Caroline Jirka; Jasmine H Pak; Claire A Grosgogeat; Michael Mario Marchetii; Vandana A Gupta
Journal:  Hum Mol Genet       Date:  2019-08-01       Impact factor: 6.150

10.  Invasion of normal human fibroblasts induced by v-Fos is independent of proliferation, immortalization, and the tumor suppressors p16INK4a and p53.

Authors:  Linda A Scott; J Keith Vass; E Kenneth Parkinson; David A F Gillespie; Joseph N Winnie; Bradford W Ozanne
Journal:  Mol Cell Biol       Date:  2004-02       Impact factor: 4.272

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