Please use this identifier to cite or link to this item:
Title: The function of ORAOV1/LTO1, a gene that is overexpressed frequently in cancer: Essential roles in the function and biogenesis of the ribosome
Authors: Zhai, Chao 
Li, Y. 
Mascarenhas, Claire 
Lin, Qiushi 
Li, Kuoyu 
Vyrides, Ioannis 
Grant, Chris M. 
Panaretou, Barry 
Keywords: Fe-S cluster;Ribosome biogenesis;Squamous cell carcinoma;Translation
Category: Clinical Medicine
Field: Medical and Health Sciences
Issue Date: 23-Jan-2014
Publisher: Nature Publishing Group
Source: Oncogene, 2014, Volume 33, Issue 4, Pages 484-494
Abstract: ORAOV1 (oral cancer overexpressed) is overexpressed in many solid tumours, making a key contribution to the development of cancer, but the cellular role of ORAOV1 is unknown. The yeast orthologue of this protein is encoded by the hitherto uncharacterized essential gene, YNL260c. Expression of ORAOV1 restores viability to yeast cells lacking YNL260c. Under nonpermissive conditions, our conditional mutants of YNL260c are defective in the maturation of the 60S ribosomal subunit, whereas maturation of the 40S subunit is unaffected. Also, initiation of translation is abrogated when YNL260c function is lost. YNL260c is indispensible for life in oxygen, but is nonessential under anaerobic conditions. Consequently, the toxic affects of aerobic metabolism on biogenesis and function of the ribosome are alleviated by YNL260c, hence, we rename YNL260c as LTO1; required for biogenesis of the large ribosomal subunit and initiation of translation in oxygen. Lto1 is found in a complex with Rli1/ABCE1, an ATP-binding cassette (ABC)-ATPase bearing N-terminal 4Fe-4S clusters. Like Lto1, the Rli1/ABCE1 4Fe-4S clusters are not required for viability under anaerobic conditions, but are essential in the presence of oxygen. Loss of Lto1 function renders cells susceptible to hydroperoxide pro-oxidants, though this type of sensitivity is specific to certain types of oxidative stress as the lto1 mutants are not sensitive to an agent that oxidizes thiols. These findings reflect a functional interaction between Lto1 and the Rli1/ABCE1 4Fe-4S clusters, as part of a complex, which relieves the toxic effects of reactive oxygen species (ROS) on biogenesis and function of the ribosome. This complex also includes Yae1, which bridges the interaction between Lto1 and Rli1/ABCE1. Interactions between members of this complex were demonstrated both in vivo and in vitro. An increased generation of ROS is a feature shared by many cancers. The ORAOV1 complex could prevent ROS-induced ribosomal damage, explaining why overexpression of ORAOV1 is so common in solid tumours.
ISSN: 09509232
DOI: 10.1038/onc.2012.604
Rights: © 2014 Macmillan Publishers Limited All rights reserved.
Type: Article
Appears in Collections:Άρθρα/Articles

Show full item record

Citations 20

checked on Oct 6, 2019

Page view(s) 20

Last Week
Last month
checked on Oct 13, 2019

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.