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Biology subjects

Dutt, P.

Publications and source records attributed to Dutt, P..

2 recordsLinked to original sources

NEK10 tyrosine phosphorylates β-catenin to regulate its cytoplasmic turnover.

Nek kinases are involved in regulating several different elements of the centrosomal cycle, primary cilia function, and DNA damage responses. Unlike the other members of the Nek family, which are serine-threonine kinases, Nek10 preferentially targets tyrosines. Nek10 appears to have a broad role in DNA damage responses, regulating a MAPK-activated G2/M checkpoint following UV irradiation and influencing the p53-mediated activation induced by genotoxicity. In an attempt to identify additional Nek10 functions, we characterized the effect of Nek10 deletion in lung cancer cells, where it is relatively highly expressed. Nek10 absence led to an increase in both the signaling and adherens junctions pools of {beta}-catenin. Mechanistically, Nek10 associates with the Axin complex where it phosphorylates {beta}-catenin at Tyr30, located within the regulatory region governing {beta}-catenin turnover. In the absence of Nek10 phosphorylation, GSK3-mediated phosphorylation of {beta}-catenin, a prerequisite for its turnover, was significantly impaired. Stabilization of {beta}-catenin driven by Nek10 loss diminished the ability of cells to form tumorspheres in suspension, grow in soft agar, and colonize mouse lung tissue following tail vein injections.

cancer biology↗

NEK10 tyrosine phosphorylates p53 and controls its transcriptional activity

In response to genotoxic stress, multiple kinase signalling cascades are activated, many of them directed towards the tumour suppressor p53 which coordinates the DNA damage response (DDR). Defects in DDR pathways lead to an accumulation of mutations that can promote tumorigenesis. Emerging evidence implicates multiple members of the NimA-related kinase (NEK) family (NEK1, NEK10 and NEK11) in the DDR. Here, we describe a function for NEK10 in the regulation of p53 transcriptional activity through tyrosine phosphorylation. NEK10 loss increases cellular proliferation through modulation of the p53-dependent transcriptional output, by directly phosphorylating p53 on Y327, revealing NEK10s unexpected substrate specificity. A p53 mutant at this site (Y327F) acts as a hypomorph, causing an attenuated p53-mediated transcriptional response. Consistently, NEK10-deficient cells display heightened sensitivity to DNA damaging agents and low NEK10 expression is an independent predictor of a favorable response to radiation treatment in WT TP53 breast cancer patients.

cancer biology↗