Transfer RNA Methytransferases and Their Corresponding Modifications in Budding Yeast and Humans: Activities, Predications, and Potential Roles in Human Health

被引:75
作者
Towns, William L. [1 ]
Begley, Thomas J. [1 ,2 ,3 ]
机构
[1] SUNY Albany, Coll Nanoscale Sci & Engn, Albany, NY 12203 USA
[2] SUNY Albany, RNA Inst, Rensselaer, NY USA
[3] SUNY Albany, Canc Res Ctr, Rensselaer, NY USA
关键词
PHENYLALANINE TRANSFER-RNA; LINKED MENTAL-RETARDATION; BINDING PROTEIN ABP140; METHIONYL-TRANSFER-RNA; HUMAN ALKB HOMOLOG; SACCHAROMYCES-CEREVISIAE; ESCHERICHIA-COLI; S-ADENOSYLMETHIONINE; ENDO-EXONUCLEASE; BREAST-CANCER;
D O I
10.1089/dna.2011.1437
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Throughout the kingdoms of life, transfer RNA (tRNA) undergoes over 100 enzyme-catalyzed, methyl-based modifications. Although a majority of the methylations are conserved from bacteria to mammals, the functions of a number of these modifications are unknown. Many of the proteins responsible for tRNA methylation, named tRNA methyltransferases (Trms), have been characterized in Saccharomyces cerevisiae. In contrast, only a few human Trms have been characterized. A BLAST search for human homologs of each S. cerevisiae Trm revealed a total of 34 human proteins matching our search criteria for an S. cerevisiae Trm homolog candidate. We have compiled a database cataloging basic information about each human and yeast Trm. Every S. cerevisiae Trm has at least one human homolog, while several Trms have multiple candidates. A search of cancer cell versus normal cell mRNA expression studies submitted to Oncomine found that 30 of the homolog genes display a significant change in mRNA expression levels in at least one data set. While 6 of the 34 human homolog candidates have confirmed tRNA methylation activity, the other candidates remain uncharacterized. We believe that our database will serve as a resource for investigating the role of human Trms in cellular stress signaling.
引用
收藏
页码:434 / 454
页数:21
相关论文
共 108 条
[1]   Rapid tRNA decay can result from lack of nonessential modifications [J].
Alexandrov, A ;
Chernyakov, I ;
Gu, WF ;
Hiley, SL ;
Hughes, TR ;
Grayhack, EJ ;
Phizicky, EM .
MOLECULAR CELL, 2006, 21 (01) :87-96
[2]   tRNA m7G methyltransferase Trm8p/Trm82p:: Evidence linking activity to a growth phenotype and implicating Trm82p in maintaining levels of active Trm8p [J].
Alexandrov, A ;
Grayhack, EJ ;
Phizicky, EM .
RNA, 2005, 11 (05) :821-830
[3]   Two proteins that form a complex are required for 7-methylguanosine modification of yeast tRNA [J].
Alexandrov, A ;
Martzen, MR ;
Phizicky, EM .
RNA, 2002, 8 (10) :1253-1266
[4]   The Gcd10p/Gcd14p complex is the essential two-subunit tRNA(1-methyladenosine) methyltransferase of Saccharomyces cerevisiae [J].
Anderson, J ;
Phan, L ;
Hinnebusch, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5173-5178
[5]   The essential Gcd10p-Gcd14p nuclear complex is required for 1-methyladenosine modification and maturation of initiator methionyl-tRNA [J].
Anderson, J ;
Phan, L ;
Cuesta, R ;
Carlson, BA ;
Pak, M ;
Asano, K ;
Björk, GR ;
Tamame, M ;
Hinnebusch, AG .
GENES & DEVELOPMENT, 1998, 12 (23) :3650-3662
[6]   A novel CHHC Zn-finger domain found in spliceosomal proteins and tRNA modifying enzymes [J].
Andreeva, Antonina ;
Tidow, Henning .
BIOINFORMATICS, 2008, 24 (20) :2277-2280
[7]   Isolation and characterization of a novel actin filament-binding protein from Saccharomyces cerevisiae [J].
Asakura, T ;
Sasaki, T ;
Nagano, F ;
Satoh, A ;
Obaishi, H ;
Nishioka, H ;
Imamura, H ;
Hotta, K ;
Tanaka, K ;
Nakanishi, H ;
Takai, Y .
ONCOGENE, 1998, 16 (01) :121-130
[8]   Genetic analysis of the yeast NUD1 endo-exonuclease:: a role in the repair of DNA double-strand breaks [J].
Asefa, B ;
Kauler, P ;
Cournoyer, D ;
Lehnert, S ;
Chow, TYK .
CURRENT GENETICS, 1998, 34 (05) :360-367
[9]   Molecular analysis of METTL1, a novel human methyltransferase-like gene with a high degree of phylogenetic conservation [J].
Bahr, A ;
Hankeln, T ;
Fiedler, T ;
Hegemann, J ;
Schmidt, ER .
GENOMICS, 1999, 57 (03) :424-428
[10]   Mammostrat® as a tool to stratify breast cancer patients at risk of recurrence during endocrine therapy [J].
Bartlett, John M. S. ;
Thomas, Jeremy ;
Ross, Douglas T. ;
Seitz, Robert S. ;
Ring, Brian Z. ;
Beck, Rodney A. ;
Pedersen, Hans Christian ;
Munro, Alison ;
Kunkler, Ian H. ;
Campbell, Fiona M. ;
Jack, Wilma ;
Kerr, Gillian R. ;
Johnstone, Laura ;
Cameron, David A. ;
Chetty, Udi .
BREAST CANCER RESEARCH, 2010, 12 (04)