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CKH2/PKL 染色质重塑因子负调控拟南芥愈伤组织中的细胞分裂素反应。

The CKH2/PKL chromatin remodeling factor negatively regulates cytokinin responses in Arabidopsis calli.

机构信息

Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 Japan.

出版信息

Plant Cell Physiol. 2011 Apr;52(4):618-28. doi: 10.1093/pcp/pcr022. Epub 2011 Feb 25.

Abstract

Cytokinins promote cell division and chloroplast development in tissue culture. We previously isolated two mutants of Arabidopsis thaliana, ckh1 (cytokinin-hypersensitive 1) and ckh2, which produce rapidly growing green calli in response to lower levels of cytokinins than those found in the wild type. Here we report that the product of the CKH2 gene is PICKLE, a protein resembling the CHD3 class of SWI/SNF chromatin remodeling factors. We also show that inhibition of histone deacetylase by trichostatin A (TSA) partially substituted for cytokinins, but not for auxin, in the promotion of callus growth, indicating that chromatin remodeling and histone deacetylation are intimately related to cytokinin-induced callus growth. A microarray experiment revealed that either the ckh1 mutation or the ckh2 mutation caused hypersensitivity to cytokinins in terms of gene expression, especially of photosynthesis-related genes. The ckh1 and ckh2 mutations up-regulated nuclear-encoded genes, but not plastid-encoded genes, whereas TSA deregulated both nuclear- and plastid-encoded genes. The ckh1 ckh2 double mutant showed synergistic phenotypes: the callus grew with a green color independently of exogenous cytokinins. A yeast two-hybrid experiment showed protein interaction between CKH1/EER4/AtTAF12b and CKH2/PKL. These results suggest that CKH1/EER4/AtTAF12b and CKH2/PKL may act together on cytokinin-regulated genes.

摘要

细胞分裂素促进组织培养中的细胞分裂和叶绿体发育。我们之前分离到拟南芥的两个突变体,ckh1(细胞分裂素超敏 1)和 ckh2,它们在低于野生型水平的细胞分裂素刺激下产生快速生长的绿色愈伤组织。在这里,我们报告说 CKH2 基因的产物是 PICKLE,一种类似于 CHD3 类 SWI/SNF 染色质重塑因子的蛋白质。我们还表明,组蛋白去乙酰化酶抑制剂曲古抑菌素 A(TSA)部分替代细胞分裂素,但不替代生长素,促进愈伤组织生长,表明染色质重塑和组蛋白去乙酰化与细胞分裂素诱导的愈伤组织生长密切相关。微阵列实验表明,ckh1 突变或 ckh2 突变导致在基因表达方面对细胞分裂素敏感,尤其是与光合作用相关的基因。ckh1 和 ckh2 突变上调核编码基因,但不上调质体编码基因,而 TSA 则使核编码基因和质体编码基因都失活。ckh1 ckh2 双突变体表现出协同表型:愈伤组织在不依赖外源细胞分裂素的情况下呈绿色生长。酵母双杂交实验表明 CKH1/EER4/AtTAF12b 和 CKH2/PKL 之间存在蛋白相互作用。这些结果表明,CKH1/EER4/AtTAF12b 和 CKH2/PKL 可能共同作用于细胞分裂素调节的基因。

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