Transcriptional Control of SET DOMAIN GROUP 8 and CAROTENOID ISOMERASE during Arabidopsis Development

被引:59
作者
Cazzonelli, Christopher I. [1 ]
Roberts, Andrea C. [1 ]
Carmody, Melanie E. [1 ]
Pogson, Barry J. [1 ]
机构
[1] Australian Natl Univ, Res Sch Biol, Australian Res Council Ctr Excellence Plant Energ, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会;
关键词
Photosynthesis; secondary metabolism-terpenoids; isoprenoids; and carotenoids; chloroplast biology; epigenetics; gene expression; gene regulation; PROLAMELLAR BODY FORMATION; GENOME-WIDE ANALYSIS; LOCUS-C EXPRESSION; GENE-EXPRESSION; BIOSYNTHETIC-PATHWAY; PHYTOENE SYNTHASE; IN-VITRO; PROMOTER; STRESS; LIGHT;
D O I
10.1093/mp/ssp092
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
Carotenoids are pigments required for photosynthesis, photoprotection and the production of carotenoid-derived hormones such as ABA and strigolactones. The carotenoid biosynthetic pathway bifurcates after lycopene to produce epsilon- and beta-carotenoids and this branch is critical for determining carotenoid composition. Here, we show how the branch point can be regulated by the chromatin-modifying histone methyltransferase, Set Domain Group 8 (SDG8) targeting the carotenoid isomerase (CRTISO). SDG8 is required to maintain permissive expression of CRTISO during seedling development, in leaves, shoot apex, and some floral organs. The CRTISO and SDG8 promoters show overlapping tissue-specific patterns of reporter gene activity. Interestingly, CRTISO showed atypical reporter gene expression in terms of greater variability between different lines compared to the Cauliflower Mosaic Virus 35S promoter (CaMV35s) and epsilon LCY promoters, potentially due to chromosomal position effects. Regulation of the CRTISO promoter was dependent in part upon the presence or absence of SDG8. Knockouts of SDG8 (carotenoid and chloroplast regulation (ccr1)) and CRTISO (ccr2) result in altered carotenoid composition and this could be restored in ccr2 using the CaMV35s or CRTISO promoters. In contrast, varying degrees of GUS expression and carotenoid complementation by CRTISO overexpression using CaMV35S or CRTISO promoters in the ccr1 background demonstrated that both the CRTISO promoter and open reading frame are necessary for SDG8-mediated expression of CRTISO.
引用
收藏
页码:174 / 191
页数:18
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