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表皮发育依赖于 YABBY 蛋白 INNER NO OUTER 与共激活子和共抑制子的相互作用。

Integument Development in Depends on Interaction of YABBY Protein INNER NO OUTER with Coactivators and Corepressors.

机构信息

Department of Molecular and Cellular Biology, University of California, Davis, California 95616.

Department of Molecular and Cellular Biology, University of California, Davis, California 95616

出版信息

Genetics. 2017 Dec;207(4):1489-1500. doi: 10.1534/genetics.117.300140. Epub 2017 Sep 29.

Abstract

INNER NO OUTER (INO) is a YABBY protein that is essential for the initiation and development of the outer integument of ovules. Other YABBY proteins have been shown to be involved in both negative and positive regulation of expression of putative target genes. YABBY proteins have also been shown to interact with the corepressor LEUNIG (LUG) in several systems. In support of a repressive role for INO, we confirm that INO interacts with LUG and also find that INO directly interacts with SEUSS (SEU), a known corepressive partner of LUG. Further, we find that INO can directly interact with ADA2b/PROPORZ1 (PRZ1), a transcriptional coactivator that is known to interact with the histone acetyltransferase GENERAL CONTROL NONREPRESSIBLE PROTEIN 5 (GCN5, also known as HAG1). Mutations in , , and / all lead to pleiotropic effects including a deficiency in the extension of the outer integument. Additive and synergistic effects of / and mutations on outer integument formation indicate that these two genes function independently to promote outer integument growth. The mutation is epistatic to both and / in the outer integument, and all three proteins are present in the nuclei of a common set of outer integument cells. This is consistent with a model where INO utilizes these coregulator proteins to activate and repress separate sets of target genes. Other YABBY proteins were shown to also form complexes with ADA2b/PRZ1, and have been previously shown to interact with SEU and LUG. Thus, interaction with these corepressors and coactivator may represent a general mechanism to explain the positive and negative activities of YABBY proteins in transcriptional regulation. The LUG, SEU, and ADA2b/PRZ1 proteins would also separately be recruited to targets of other transcription factors, consistent with their roles as general coregulators, explaining the pleiotropic effects not associated with YABBY function.

摘要

内无外(INO)是一种 YABBY 蛋白,对于胚珠外珠被的起始和发育是必不可少的。其他 YABBY 蛋白已被证明参与了假定靶基因表达的正调控和负调控。YABBY 蛋白还被证明在几个系统中与共抑制子 LEUNIG(LUG)相互作用。为了支持 INO 的抑制作用,我们证实 INO 与 LUG 相互作用,并且还发现 INO 直接与 SEUSS(SEU)相互作用,SEU 是 LUG 的已知共抑制子伙伴。此外,我们发现 INO 可以直接与 ADA2b/PROPORZ1(PRZ1)相互作用,PRZ1 是一种已知的转录共激活因子,已知与组蛋白乙酰转移酶 GENERAL CONTROL NONREPRESSIBLE PROTEIN 5(GCN5,也称为 HAG1)相互作用。、和 / 的突变导致多种表型效应,包括外珠被延伸缺陷。/ 和 突变对外珠被形成的累加和协同效应表明这两个基因独立作用以促进外珠被生长。突变在外珠被中对 和 / 是上位的,并且这三个蛋白都存在于一组共同的外珠被细胞的核中。这与 INO 利用这些共调节蛋白来激活和抑制独立的靶基因集的模型一致。其他 YABBY 蛋白也被证明与 ADA2b/PRZ1 形成复合物,并且先前已被证明与 SEU 和 LUG 相互作用。因此,与这些共抑制子和共激活因子的相互作用可能代表了一个解释 YABBY 蛋白在转录调控中的正调控和负调控的一般机制。LUG、SEU 和 ADA2b/PRZ1 蛋白也将分别被招募到其他转录因子的靶标上,这与它们作为通用共调节子的作用一致,解释了与 YABBY 功能无关的多效性效应。

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