玉米代谢性状基因调控变异的分子机制。

IF 10 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Plant Cell Pub Date : 2024-09-03 DOI:10.1093/plcell/koae180
Yi-Hsuan Chu, Yun Sun Lee, Fabio Gomez-Cano, Lina Gomez-Cano, Peng Zhou, Andrea I Doseff, Nathan Springer, Erich Grotewold
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引用次数: 0

摘要

基因表达水平的差异普遍存在于个体、种族或品种之间,并对农艺产生重大影响,例如,会影响杂交种的活力。基因表达水平的变异来自于调控序列(顺式)和/或转录因子(TF)活性(反式)的突变,但复杂表型的顺式和/或反式调控变异的内在机制在很大程度上仍然未知。在此,我们研究了两种广泛使用的玉米(Zea mays)近交系 B73 和 A632 的丝中杀虫化合物麦黄素和绿原酸的不同积累的基因表达变异机制。通过结合转录组学和表观组学,我们确定了玉米 R2R3-MYB TF Pericarp color1(P1)的 1338 个蚕丝直接靶标,这与它是麦黄素和绿原酸生物合成的调控因子是一致的。在这些 P1 靶标中,464 个靶标在 B73 和 A632 蚕丝间表现出等位基因特异性表达(ASE)。等位基因 DNA 亲和纯化测序发现了 34 个 P1 等位基因特异性结合(ASB)与顺式表达变化相关的例子。从先前的酵母单杂交研究中,我们发现了可能与 P1 目标控制有关的 9 个 TFs,464 个 ASE 基因中有 83 个基因(顺式)与 ASB 有关,9 个 TFs 中有 4 个在 B73 和 A632 丝之间有差异表达(反式)。这些结果为了解基因表达水平自然变异的普遍机制以及如何建立代谢多样性调控提供了一个分子框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular mechanisms underlying gene regulatory variation of maize metabolic traits.

Variation in gene expression levels is pervasive among individuals and races or varieties, and has substantial agronomic consequences, for example, by contributing to hybrid vigor. Gene expression level variation results from mutations in regulatory sequences (cis) and/or transcription factor (TF) activity (trans), but the mechanisms underlying cis- and/or trans-regulatory variation of complex phenotypes remain largely unknown. Here, we investigated gene expression variation mechanisms underlying the differential accumulation of the insecticidal compounds maysin and chlorogenic acid in silks of widely used maize (Zea mays) inbreds, B73 and A632. By combining transcriptomics and cistromics, we identified 1,338 silk direct targets of the maize R2R3-MYB TF Pericarp color1 (P1), consistent with it being a regulator of maysin and chlorogenic acid biosynthesis. Among these P1 targets, 464 showed allele-specific expression (ASE) between B73 and A632 silks. Allelic DNA-affinity purification sequencing identified 34 examples in which P1 allelic specific binding (ASB) correlated with cis-expression variation. From previous yeast one-hybrid studies, we identified 9 TFs potentially implicated in the control of P1 targets, with ASB to 83 out of 464 ASE genes (cis) and differential expression of 4 out of 9 TFs between B73 and A632 silks (trans). These results provide a molecular framework for understanding universal mechanisms underlying natural variation of gene expression levels, and how the regulation of metabolic diversity is established.

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来源期刊
Plant Cell
Plant Cell 生物-生化与分子生物学
CiteScore
16.90
自引率
5.20%
发文量
337
审稿时长
2.4 months
期刊介绍: Title: Plant Cell Publisher: Published monthly by the American Society of Plant Biologists (ASPB) Produced by Sheridan Journal Services, Waterbury, VT History and Impact: Established in 1989 Within three years of publication, ranked first in impact among journals in plant sciences Maintains high standard of excellence Scope: Publishes novel research of special significance in plant biology Focus areas include cellular biology, molecular biology, biochemistry, genetics, development, and evolution Primary criteria: articles provide new insight of broad interest to plant biologists and are suitable for a wide audience Tenets: Publish the most exciting, cutting-edge research in plant cellular and molecular biology Provide rapid turnaround time for reviewing and publishing research papers Ensure highest quality reproduction of data Feature interactive format for commentaries, opinion pieces, and exchange of information in review articles, meeting reports, and insightful overviews.
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