Weight-induced radial growth in plant stems depends on PIN3

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Àngela Carrió-Seguí, Paula Brunot-Garau, Cristina Úrbez, Pál Miskolczi, Francisco Vera-Sirera, Hannele Tuominen, Javier Agustí
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引用次数: 0

Abstract

How multiple growth programs coordinate during development is a fundamental question in biology. During plant stem development, radial growth is continuously adjusted in response to longitudinal-growth-derived weight increase to guarantee stability.1,2,3 Here, we demonstrate that weight-stimulated stem radial growth depends on the auxin efflux carrier PIN3, which, upon weight increase, expands its cellular localization from the lower to the lateral sides of xylem parenchyma, phloem, procambium, and starch sheath cells, imposing a radial auxin flux that results in radial growth. Using the protein synthesis inhibitor cycloheximide (CHX) or the fluorescent endocytic tracer FM4-64, we reveal that this expansion of the PIN3 cellular localization domain occurs because weight increase breaks the balance between PIN3 biosynthesis and removal, favoring PIN3 biosynthesis. Experimentation using brefeldin A (BFA) treatments or arg1 and arl2 mutants further supports this conclusion. Analyses of CRISPR-Cas9 lines for Populus PIN3 orthologs reveals that PIN3 dependence of weight-induced radial growth is conserved at least in these woody species. Altogether, our work sheds new light on how longitudinal and radial growth coordinate during stem development.

植物茎的重量诱导径向生长取决于 PIN3
多种生长程序在发育过程中如何协调是生物学的一个基本问题。1,2,3在这里,我们证明了重量刺激下的茎径向生长依赖于辅素外流载体PIN3,当重量增加时,PIN3将其细胞定位从木质部实质、韧皮部、原生质和淀粉鞘细胞的下部扩展到侧部,形成径向辅素通量,导致径向生长。利用蛋白质合成抑制剂环己亚胺(CHX)或荧光内细胞示踪剂 FM4-64,我们揭示了 PIN3 细胞定位域的扩大是因为重量的增加打破了 PIN3 生物合成和清除之间的平衡,有利于 PIN3 的生物合成。使用溴苯胍 A(BFA)处理或 arg1 和 arl2 突变体进行的实验进一步支持了这一结论。对杨树 PIN3 同源物的 CRISPR-Cas9 株系分析表明,至少在这些木本物种中,PIN3 对重量诱导的径向生长的依赖性是保守的。总之,我们的工作为了解茎发育过程中纵向和径向生长如何协调提供了新的线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
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