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有助于在小麦减数分裂过程中维持同源和部分同源重组。

contributes to maintain both homologous and homoeologous recombination during wheat meiosis.

作者信息

Bazile Jeanne, Nadaud Isabelle, Lasserre-Zuber Pauline, Kitt Jonathan, De Oliveira Romain, Choulet Frédéric, Sourdille Pierre

机构信息

INRAE, UMR 1095 INRAE - UCA Genetics, Diversity & Ecophysiology of Cereals, Clermont-Ferrand, France.

Biotech Research and Innovation Centre (BRIC), Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Front Plant Sci. 2024 Jan 29;14:1342976. doi: 10.3389/fpls.2023.1342976. eCollection 2023.

Abstract

INTRODUCTION

Meiotic recombination (or crossover, CO) is essential for gamete fertility as well as for alleles and genes reshuffling that is at the heart of plant breeding. However, CO remains a limited event, which strongly hampers the rapid production of original and improved cultivars. is a gene encoding a helicase protein that, when mutated, contributes to improve recombination rate in all species where it has been evaluated so far.

METHODS

In this study, we developed wheat ( L.) triple mutant (TM) for the three homoeologous copies of as well as mutants for two copies and heterozygous for the last one (Htz-A, Htz-B, Htz-D).

RESULTS

Phenotypic observation revealed a significant reduction of fertility and pollen viability in TM and Htz-B plants compared to wild type plants suggesting major defects during meiosis. Cytogenetic analyses of these plants showed that complete absence of as observed in TM plants, leads to chromosome fragmentation during the pachytene stage, resulting in problems in the segregation of chromosomes during meiosis. Htz-A and Htz-D mutants had an almost normal meiotic progression indicating that both and copies are functional and that there is no dosage effect for in bread wheat. On the contrary, the copy seems knocked-out, probably because of a SNP leading to a Threonine>Alanine change at position 539 (T539A) of the protein, that occurs in the crucial helicase ATP bind/DEAD/ResIII domain which unwinds nucleic acids. Occurrence of numerous multivalents in TM plants suggests that could also play a role in the control of homoeologous recombination.

DISCUSSION

These findings provide a foundation for further molecular investigations into wheat meiosis regulation to fully understand the underlying mechanisms of how affects chiasma formation, as well as to identify ways to mitigate these defects and enhance both homologous and homoeologous recombination efficiency in wheat.

摘要

引言

减数分裂重组(或交叉互换,CO)对于配子育性以及等位基因和基因重排至关重要,而基因重排是植物育种的核心。然而,交叉互换仍然是一个有限的事件,这严重阻碍了新型和改良品种的快速培育。 是一个编码解旋酶蛋白的基因,当它发生突变时,有助于提高在目前已评估的所有物种中的重组率。

方法

在本研究中,我们针对 的三个同源拷贝培育了小麦( )三重突变体(TM),以及针对两个拷贝的突变体和最后一个拷贝为杂合的突变体(Htz-A、Htz-B、Htz-D)。

结果

表型观察表明,与野生型植株相比,TM和Htz-B植株的育性和花粉活力显著降低,这表明减数分裂过程中存在主要缺陷。对这些植株的细胞遗传学分析表明,如在TM植株中观察到的 完全缺失,会导致粗线期染色体片段化,从而在减数分裂过程中导致染色体分离问题。Htz-A和Htz-D突变体的减数分裂进程几乎正常,这表明 和 拷贝都是有功能的,并且在面包小麦中 不存在剂量效应。相反, 拷贝似乎被敲除了,可能是由于一个单核苷酸多态性导致蛋白质第539位的苏氨酸变为丙氨酸(T539A),该突变发生在解开核酸的关键解旋酶ATP结合/DEAD/ResIII结构域中。TM植株中出现大量多价体表明 也可能在同源重组的控制中发挥作用。

讨论

这些发现为进一步对小麦减数分裂调控进行分子研究奠定了基础,以全面了解 影响交叉点形成的潜在机制,以及确定减轻这些缺陷并提高小麦同源和同源重组效率的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ae/10859459/502c90f1ba0a/fpls-14-1342976-g001.jpg

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