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突变体中独脚金内酯受体活性的快速分析

Rapid analysis of strigolactone receptor activity in a mutant.

作者信息

White Alexandra R F, Mendez Jose A, Khosla Aashima, Nelson David C

机构信息

Department of Botany and Plant Sciences University of California Riverside California USA.

出版信息

Plant Direct. 2022 Mar 25;6(3):e389. doi: 10.1002/pld3.389. eCollection 2022 Mar.

Abstract

DWARF14 (D14) is an ɑ/β-hydrolase and receptor for the plant hormone strigolactone (SL) in angiosperms. Upon SL perception, D14 works with MORE AXILLARY GROWTH2 (MAX2) to trigger polyubiquitination and degradation of DWARF53(D53)-type proteins in the SUPPRESSOR OF MAX2 1-LIKE (SMXL) family. We used CRISPR-Cas9 to generate knockout alleles of the two homoeologous genes in the genome. The double mutant had several phenotypes that are consistent with the loss of SL perception in other plants, including increased axillary bud outgrowth, reduced height, shortened petioles, and smaller leaves. A ratiometric fluorescent reporter system was used to monitor degradation of SMXL7 from (AtSMXL7) after transient expression in and treatment with the strigolactone analog GR24. AtSMXL7 was degraded after treatment with GR24, which has the stereochemical configuration of natural SLs, as well as its enantiomer GR24 . In leaves, AtSMXL7 abundance was unaffected by -GR24 or either GR24 stereoisomer. Transient coexpression of AtD14 with the AtSMXL7 reporter in restored the degradation response to -GR24, but required an active catalytic triad. We used this platform to evaluate the ability of several AtD14 mutants that had not been characterized in plants to target AtSMXL7 for degradation.

摘要

DWARF14(D14)是一种α/β水解酶,也是被子植物中植物激素独脚金内酯(SL)的受体。在感知到SL后,D14与多侧芽生长2(MAX2)共同作用,触发MAX2抑制因子1样(SMXL)家族中DWARF53(D53)型蛋白的多聚泛素化和降解。我们使用CRISPR-Cas9在基因组中产生了两个同源基因的敲除等位基因。该双突变体具有多种与其他植物中SL感知丧失一致的表型,包括腋芽生长增加、株高降低、叶柄缩短和叶片变小。使用比率荧光报告系统监测拟南芥中瞬时表达并经独脚金内酯类似物GR24处理后AtSMXL7(来自拟南芥的SMXL7)的降解情况。用具有天然SL立体化学构型的GR24及其对映体GR24处理后,AtSMXL7被降解。在拟南芥叶片中,AtSMXL7的丰度不受对映体GR24或任何一种GR24立体异构体的影响。AtD14与AtSMXL7报告基因在拟南芥中的瞬时共表达恢复了对映体GR24的降解反应,但需要一个活性催化三联体。我们利用这个平台评估了几个尚未在植物中表征的AtD14突变体将AtSMXL7靶向降解的能力。

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