期刊
CELLULAR SIGNALLING
卷 19, 期 6, 页码 1309-1314出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2007.01.010
关键词
phosphatidylinositol 5-phosphate; phosphatidylinositol 5-phosphate 4-kinase; DT40 cells; genomic tagging
类别
资金
- Medical Research Council [MC_U105178811] Funding Source: Medline
- Wellcome Trust [079194, 063581] Funding Source: Medline
- MRC [MC_U105178811] Funding Source: UKRI
- Medical Research Council [MC_U105178811] Funding Source: researchfish
Previous studies from acutely transfected HeLa cells have identified an acidic alpha-helix in the Type II beta PtdIns5P 4-kinase (PIPkin II beta) as a putative novel nuclear localisation sequence (Ciruela et al. Biochem. J. 364, 587-5912000). However, some heterogeneity in cellular localisation was always observed, and other published aspects of PIPkin II beta physiology are more consistent with an extra-nuclear function. As a means of resolving whether the endogenous PIPkin II beta is nuclear, we have used the high homologous recombination frequency of DT40 cells to knock an epitope tag (Mosedale et al., Nat Struct Biol. 12, 763-771 2005) into one of the alleles of the DT40 PIPkin II beta gene. We show that PIPkin II beta is expressed as a tagged protein, is active as revealed by immunoprecipitation and enzyme assay, and that cellular fractionation reveals that it is indeed nuclear. Genomic tagging of endogenous proteins in DT40 cells is a technique that offers unique advantages in studying endogenous signalling proteins. (c) 2007 Elsevier Inc. All rights reserved.
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