INCURVATA2 encodes the catalytic subunit of DNA polymerase α and interacts with genes involved in chromatin-mediated cellular memory in Arabidopsis thaliana

被引:125
作者
Barrero, Jose Maria
Gonzalez-Bayon, Rebeca
del Pozo, Juan Carlos
Ponce, Maria Rosa
Micol, Jose Luis [1 ]
机构
[1] Univ Miguel Hernandez, Div Genet, Alicante 03202, Spain
[2] Univ Miguel Hernandez, Inst Bioingn, Alicante 03202, Spain
[3] Inst Nacl Invest & Tecnol Agraria & Alimentaria, Dept Biotecnol, Madrid 28040, Spain
关键词
D O I
10.1105/tpc.107.054130
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
Cell type-specific gene expression patterns are maintained by the stable inheritance of transcriptional states through mitosis, requiring the action of multiprotein complexes that remodel chromatin structure. Genetic and molecular interactions between chromatin remodeling factors and components of the DNA replication machinery have been identified in Schizosaccharomyces pombe, indicating that some epigenetic marks are replicated simultaneously to DNA with the participation of the DNA replication complexes. This model of epigenetic inheritance might be extended to the plant kingdom, as we report here with the positional cloning and characterization of INCURVATA2 (ICU2), which encodes the putative catalytic subunit of the DNA polymerase a of Arabidopsis thaliana. The strong icu2-2 and icu2-3 insertional alleles caused fully penetrant zygotic lethality when homozygous and incompletely penetrant gametophytic lethality, probably because of loss of DNA polymerase activity. The weak icu2-1 allele carried a point mutation and caused early flowering, leaf incurvature, and homeotic transformations of sepals into carpels and of petals into stamens. Further genetic analyses indicated that ICU2 interacts with TERMINAL FLOWER2, the ortholog of HETEROCHROMATIN PROTEIN1 of animals and yeasts, and with the Polycomb group (PcG) gene CURLY LEAF. Another PcG gene, EMBRYONIC FLOWER2, was found to be epistatic to ICU2. Quantitative RT-PCR analyses indicated that a number of regulatory genes were derepressed in the icu2-1 mutant, including genes associated with flowering time, floral meristem, and floral organ identity.
引用
收藏
页码:2822 / 2838
页数:17
相关论文
共 119 条
[1]   Epigenetic consequences of nucleosome dynamics [J].
Ahmad, K ;
Henikoff, S .
CELL, 2002, 111 (03) :281-284
[2]   Chromodomain protein Swi6-mediated role of DNA polymerase a in establishment of silencing in fission yeast. [J].
Ahmed, S ;
Saini, S ;
Arora, S ;
Singh, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :47814-47821
[3]   Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegation [J].
Ayyanathan, K ;
Lechner, MS ;
Bell, P ;
Maul, GG ;
Schultz, DC ;
Yamada, Y ;
Tanaka, K ;
Torigoe, K ;
Rauscher, FJ .
GENES & DEVELOPMENT, 2003, 17 (15) :1855-1869
[4]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[5]   Vernalization requires epigenetic silencing of FLC by histone methylation [J].
Bastow, R ;
Mylne, JS ;
Lister, C ;
Lippman, Z ;
Martienssen, RA ;
Dean, C .
NATURE, 2004, 427 (6970) :164-167
[6]  
Bates PA, 2001, PROTEINS, P39
[7]  
Bechtold N, 1998, METH MOL B, V82, P259
[8]   Arabidopsis histone acetyltransferase AtGCN5 regulates the floral meristem activity through the WUSCHEL/AGAMOUS pathway [J].
Bertrand, C ;
Bergounioux, C ;
Domenichini, S ;
Delarue, M ;
Zhou, DX .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (30) :28246-28251
[9]   Subunit interactions in the assembly of Saccharomyces cerevisiae DNA polymerase α [J].
Biswas, SB ;
Khopde, SM ;
Zhu, FX ;
Biswas, EE .
NUCLEIC ACIDS RESEARCH, 2003, 31 (08) :2056-2065
[10]   DNA POLYMERASE-ALPHA IN THE FISSION YEAST SCHIZOSACCHAROMYCES POMBE - IDENTIFICATION AND TRACING OF THE CATALYTIC SUBUNIT DURING THE CELL-CYCLE [J].
BOUVIER, D ;
PIGNEDE, G ;
DAMAGNEZ, V ;
TILLIT, J ;
DERECONDO, AM ;
BALDACCI, G .
EXPERIMENTAL CELL RESEARCH, 1992, 198 (02) :183-190