Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Plant WEE1 kinase is cell cycle regulated and removed at mitosis via the 26S proteasome machinery

Cook, Gemma Samantha, Gronlund, Anne Lentz, Siciliano, Ilario, Spadafora, Natasha D., Amini, Maryam, Herbert, Robert, Bitonti, M. Beatrice, Graumann, Katja, Francis, Dennis and Rogers, Hilary Joan ORCID: https://orcid.org/0000-0003-3830-5857 2013. Plant WEE1 kinase is cell cycle regulated and removed at mitosis via the 26S proteasome machinery. Journal of Experimental Botany 64 (7) , pp. 2093-2106. 10.1093/jxb/ert066

Full text not available from this repository.

Abstract

In yeasts and animals, premature entry into mitosis is prevented by the inhibitory phosphorylation of cyclin-dependent kinase (CDK) by WEE1 kinase, and, at mitosis, WEE1 protein is removed through the action of the 26S proteasome. Although in higher plants WEE1 function has been confirmed in the DNA replication checkpoint, Arabidopsis wee1 insertion mutants grow normally, and a role for the protein in the G2/M transition during an unperturbed plant cell cycle is yet to be confirmed. Here data are presented showing that the inhibitory effect of WEE1 on CDK activity in tobacco BY-2 cell cultures is cell cycle regulated independently of the DNA replication checkpoint: it is high during S-phase but drops as cells traverse G2 and enter mitosis. To investigate this mechanism further, a yeast two-hybrid screen was undertaken to identify proteins interacting with Arabidopsis WEE1. Three F-box proteins and a subunit of the proteasome complex were identified, and bimolecular fluorescence complementation confirmed an interaction between AtWEE1 and the F-box protein SKP1 INTERACTING PARTNER 1 (SKIP1). Furthermore, the AtWEE1–green fluorescent protein (GFP) signal in Arabidopsis primary roots treated with the proteasome inhibitor MG132 was significantly increased compared with mock-treated controls. Expression of AtWEE1–YFPC (C-terminal portion of yellow fluorescent protein) or AtWEE1 per se in tobacco BY-2 cells resulted in a premature increase in the mitotic index compared with controls, whereas co-expression of AtSKIP1–YFPN negated this effect. These data support a role for WEE1 in a normal plant cell cycle and its removal at mitosis via the 26S proteasome.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
Subjects: Q Science > QK Botany
Uncontrolled Keywords: Arabidopsis thaliana; bimolecular fluorescence complementation (BiFC); BY-2 cell line; CDKA/B; cell cycle; F-box; green fluorescent protein (GFP); mitosis; Nicotiana tabacum; 26S proteasome SKIP1; WEE1
Publisher: Oxford University Press
ISSN: 0022-0957
Last Modified: 10 Mar 2024 17:35
URI: https://orca.cardiff.ac.uk/id/eprint/47565

Citation Data

Cited 21 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item