Laboratory of Biochemistry, Graduate School of Bioagricultural Science, Nagoya University, Chikusa, Nagoya 464-8601, Japan.
Plant J. 2009 Nov;60(3):476-87. doi: 10.1111/j.1365-313X.2009.03967.x. Epub 2009 Jul 6.
Although an APETALA2 (AP2)-type transcription factor, WRINKLED1 (WRI1), has been shown to be required for accumulation of triacylglycerols (TAGs) in Arabidopsis seeds, its direct target genes have not been established. Overexpression of WRI1 up-regulated a set of genes involved in fatty acid (FA) synthesis in plastids, including genes for a subunit of pyruvate kinase (Pl-PKbeta1), acetyl-CoA carboxylase (BCCP2), acyl carrier protein (ACP1), and ketoacyl-acyl carrier protein synthase (KAS1), while expression of these genes is reduced in mutants with reduced WRI1 expression. Transient expression of LUC reporter genes with the proximal sequences upstream from the ATG codon of Pl-PKbeta1, BCCP2, and KAS1 in protoplasts was activated by co-expression of WRI1, and recombinant WRI1 bound to these upstream sequences in vitro. The seven WRI1 binding sites shared a sequence CnTnG(7)[CG], where n is any nucleotide designated as the AW-box, and mutations in AW-boxes near the transcription start site and in the 5'-untranslated region of Pl-PKbeta1 abolished activation by WRI1 in protoplasts and expression during seed maturation. Although expression of genes for the synthesis of TAGs and packaging into oil bodies in the endoplasmic reticulum in developing seeds required WRI1, their expression was not up-regulated by WRI1 overexpression. Thus, WRI1 promotes the flow of carbon to oil during seed maturation by directly activating genes involved in FA synthesis and controlling genes for assembly and storage of TAG.
虽然 APETALA2(AP2)- 型转录因子 WRINKLED1(WRI1)已被证明是拟南芥种子中三酰基甘油(TAG)积累所必需的,但尚未确定其直接靶基因。WRI1 的过表达上调了一组参与质体中脂肪酸(FA)合成的基因,包括丙酮酸激酶(Pl-PKβ1)亚基、乙酰辅酶 A 羧化酶(BCCP2)、酰基载体蛋白(ACP1)和酮酰-酰基载体蛋白合酶(KAS1)的基因,而在 WRI1 表达减少的突变体中,这些基因的表达减少。Pl-PKβ1、BCCP2 和 KAS1 的 ATG 密码子上游近端序列的 LUC 报告基因在原生质体中的瞬时表达通过 WRI1 的共表达被激活,并且重组 WRI1 在体外与这些上游序列结合。七个 WRI1 结合位点共享一个序列 CnTnG(7)[CG],其中 n 是任何被指定为 AW 框的核苷酸,并且靠近转录起始位点和 Pl-PKβ1 的 5'-非翻译区的 AW 框中的突变消除了 WRI1 在原生质体中的激活作用以及在种子成熟过程中的表达。尽管发育中的种子中内质网中 TAG 的合成和包装到油体中的基因的表达需要 WRI1,但它们的表达不受 WRI1 过表达的上调。因此,WRI1 通过直接激活参与 FA 合成的基因并控制 TAG 组装和储存的基因,促进种子成熟过程中碳向油的流动。