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截短的ATHB17蛋白在玉米中的表达增加了抽丝期的穗重。

Expression of a truncated ATHB17 protein in maize increases ear weight at silking.

作者信息

Rice Elena A, Khandelwal Abha, Creelman Robert A, Griffith Cara, Ahrens Jeffrey E, Taylor J Philip, Murphy Lesley R, Manjunath Siva, Thompson Rebecca L, Lingard Matthew J, Back Stephanie L, Larue Huachun, Brayton Bonnie R, Burek Amanda J, Tiwari Shiv, Adam Luc, Morrell James A, Caldo Rico A, Huai Qing, Kouadio Jean-Louis K, Kuehn Rosemarie, Sant Anagha M, Wingbermuehle William J, Sala Rodrigo, Foster Matt, Kinser Josh D, Mohanty Radha, Jiang Dongming, Ziegler Todd E, Huang Mingya G, Kuriakose Saritha V, Skottke Kyle, Repetti Peter P, Reuber T Lynne, Ruff Thomas G, Petracek Marie E, Loida Paul J

机构信息

Monsanto Company, St. Louis, Missouri, United States of America.

Mendel Biotechnology Inc., Hayward, California, United States of America.

出版信息

PLoS One. 2014 Apr 15;9(4):e94238. doi: 10.1371/journal.pone.0094238. eCollection 2014.

DOI:10.1371/journal.pone.0094238
PMID:24736658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3988052/
Abstract

ATHB17 (AT2G01430) is an Arabidopsis gene encoding a member of the α-subclass of the homeodomain leucine zipper class II (HD-Zip II) family of transcription factors. The ATHB17 monomer contains four domains common to all class II HD-Zip proteins: a putative repression domain adjacent to a homeodomain, leucine zipper, and carboxy terminal domain. However, it also possesses a unique N-terminus not present in other members of the family. In this study we demonstrate that the unique 73 amino acid N-terminus is involved in regulation of cellular localization of ATHB17. The ATHB17 protein is shown to function as a transcriptional repressor and an EAR-like motif is identified within the putative repression domain of ATHB17. Transformation of maize with an ATHB17 expression construct leads to the expression of ATHB17Δ113, a truncated protein lacking the first 113 amino acids which encodes a significant portion of the repression domain. Because ATHB17Δ113 lacks the repression domain, the protein cannot directly affect the transcription of its target genes. ATHB17Δ113 can homodimerize, form heterodimers with maize endogenous HD-Zip II proteins, and bind to target DNA sequences; thus, ATHB17Δ113 may interfere with HD-Zip II mediated transcriptional activity via a dominant negative mechanism. We provide evidence that maize HD-Zip II proteins function as transcriptional repressors and that ATHB17Δ113 relieves this HD-Zip II mediated transcriptional repression activity. Expression of ATHB17Δ113 in maize leads to increased ear size at silking and, therefore, may enhance sink potential. We hypothesize that this phenotype could be a result of modulation of endogenous HD-Zip II pathways in maize.

摘要

ATHB17(AT2G01430)是拟南芥中的一个基因,编码转录因子同源异型域亮氨酸拉链II类(HD-Zip II)家族α亚类的一个成员。ATHB17单体包含所有II类HD-Zip蛋白共有的四个结构域:一个与同源异型域相邻的假定抑制结构域、亮氨酸拉链和羧基末端结构域。然而,它还拥有该家族其他成员所没有的独特N末端。在本研究中,我们证明了独特的73个氨基酸的N末端参与ATHB17细胞定位的调控。ATHB17蛋白被证明作为转录抑制因子发挥作用,并且在ATHB17的假定抑制结构域内鉴定出一个类似EAR的基序。用ATHB17表达构建体转化玉米导致ATHB17Δ113的表达,ATHB17Δ113是一种截短蛋白,缺少编码抑制结构域很大一部分的前113个氨基酸。由于ATHB17Δ113缺乏抑制结构域,该蛋白不能直接影响其靶基因的转录。ATHB17Δ113可以同二聚化,与玉米内源性HD-Zip II蛋白形成异二聚体,并结合靶DNA序列;因此,ATHB17Δ113可能通过显性负性机制干扰HD-Zip II介导的转录活性。我们提供证据表明玉米HD-Zip II蛋白作为转录抑制因子发挥作用,并且ATHB17Δ113解除这种HD-Zip II介导的转录抑制活性。ATHB17Δ113在玉米中的表达导致抽丝期穗大小增加,因此可能增强库潜力。我们推测这种表型可能是玉米内源性HD-Zip II途径受到调节的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/f31cebf5c759/pone.0094238.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/7b32954db65d/pone.0094238.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/f2e28f356857/pone.0094238.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/166a0618a93d/pone.0094238.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/e31ec346ab75/pone.0094238.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/0068e91e1845/pone.0094238.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/262cb849bf97/pone.0094238.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/31c1132dc807/pone.0094238.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/a7ff8f525c9e/pone.0094238.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/f31cebf5c759/pone.0094238.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/7b32954db65d/pone.0094238.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/f2e28f356857/pone.0094238.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/166a0618a93d/pone.0094238.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/e31ec346ab75/pone.0094238.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/0068e91e1845/pone.0094238.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/262cb849bf97/pone.0094238.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/31c1132dc807/pone.0094238.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/a7ff8f525c9e/pone.0094238.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/127d/3988052/f31cebf5c759/pone.0094238.g009.jpg

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