Structure and expression of AtPMS1, the arabidopsis ortholog of the yeast DNA repair gene PMS1

被引:14
作者
Alou, AH [1 ]
Jean, M [1 ]
Domingue, O [1 ]
Belzile, FJ [1 ]
机构
[1] Inst Nat Rech Agron Niger, Niamey, Niger
基金
加拿大自然科学与工程研究理事会;
关键词
Arabidopsis thaliana; mismatch repair; MutL homolog; PMS1; phylogenetic analysis;
D O I
10.1016/j.plantsci.2004.04.012
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
The DNA mismatch repair (MMR) machinery of eukaryotes involves several genes whose products interact to repair mispaired bases resulting from DNA replication errors or homoeologous recombination. We report here the cloning and characterization of AtPMS1, a gene that codes for a predicted polypeptide sequence of 924 amino acids containing the typical MutL motifs. It is one of three homologs of the Escherichia coli MutL gene in Arabidopsis thaliana and constitutes the first ortholog of the yeast PMS1 gene to be characterized in plants. The gene is present in a single copy in the Arabidopsis genome and is located in the top portion of chromosome IV. Northern and RT-PCR analyses indicate that the AtPMS1 gene is expressed at very low levels in mature leaves but is much more highly expressed in cultured cells. Furthermore, an alternate form of the messenger, apparently coding for an incomplete protein lacking a key portion of the C-terminus, appears to co-exist in some plant tissues, albeit at a lower abundance. Primer extension and 5'-RACE experiments suggest that this gene has multiple transcription start sites. observations that are in agreement with the lack of a detectable TATA box. These results underline the importance of experimentally-derived results to confirm and, occasionally, to correct and extend the information provided by genome projects. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:447 / 456
页数:10
相关论文
共 36 条
[1]  
Adé J, 1999, MOL GEN GENET, V262, P239
[2]   Crystal structure and ATPase activity of MutL: Implications for DNA repair and mutagenesis [J].
Ban, C ;
Yang, W .
CELL, 1998, 95 (04) :541-552
[3]   Transformation of MutL by ATP binding and hydrolysis: A switch in DNA mismatch repair [J].
Ban, C ;
Junop, M ;
Yang, W .
CELL, 1999, 97 (01) :85-97
[4]   Structural basis for MutH activation in E-coli mismatch repair and relationship of MutH to restriction endonucleases [J].
Ban, C ;
Yang, W .
EMBO JOURNAL, 1998, 17 (05) :1526-1534
[5]   In vitro cloning of complex mixtures of DNA on microbeads:: Physical separation of differentially expressed cDNAs [J].
Brenner, S ;
Williams, SR ;
Vermaas, EH ;
Storck, T ;
Moon, K ;
McCollum, C ;
Mao, JI ;
Luo, SJ ;
Kirchner, JJ ;
Eletr, S ;
DuBridge, RB ;
Burcham, T ;
Albrecht, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1665-1670
[6]   Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays [J].
Brenner, S ;
Johnson, M ;
Bridgham, J ;
Golda, G ;
Lloyd, DH ;
Johnson, D ;
Luo, SJ ;
McCurdy, S ;
Foy, M ;
Ewan, M ;
Roth, R ;
George, D ;
Eletr, S ;
Albrecht, G ;
Vermaas, E ;
Williams, SR ;
Moon, K ;
Burcham, T ;
Pallas, M ;
DuBridge, RB ;
Kirchner, J ;
Fearon, K ;
Mao, J ;
Corcoran, K .
NATURE BIOTECHNOLOGY, 2000, 18 (06) :630-634
[7]   The RNA polymerase II core promoter: a key component in the regulation of gene expression [J].
Butler, JEF ;
Kadonaga, JT .
GENES & DEVELOPMENT, 2002, 16 (20) :2583-2592
[8]   Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis [J].
Castresana, J .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (04) :540-552
[9]   DNA mismatch repair in plants - An Arabidopsis thaliana gene that predicts a protein belonging to the MSH2 subfamily of eukaryotic MutS homologs [J].
Culligan, KM ;
Hays, JB .
PLANT PHYSIOLOGY, 1997, 115 (02) :833-839
[10]   Arabidopsis MutS homologs-AtMSH2, AtMSH3, AtMSH6, and a novel AtMSH7-form three distinct protein heterodimers with different specificities for mismatched DNA [J].
Culligan, KM ;
Hays, JB .
PLANT CELL, 2000, 12 (06) :991-1002