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Tribenuron-methyl induces male sterility through anther-specific inhibition of acetolactate synthase leading to autophagic cell death

机译:曲苯磺隆通过花药特异性抑制乙酰乳酸合酶诱导雄性不育,导致自噬细胞死亡

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摘要

Tribenuron-methyl (TM) is a powerful sulfonylurea herbicide that inhibits branched-chain amino acid (BCAA) biosynthesis by targeting the catalytic subunit (CSR1) of acetolactate synthase (ALS). Selective induction of male sterility by foliar spraying of TM at low doses has been widely used for hybrid seed production in rapeseed (Brassica napus); however, the underlying mechanism remains unknown. Here, we report greater TM accumulation and subsequent stronger ALS inhibition and BCAA starvation in anthers than in leaves and stems after TM application. Constitutive or anther-specific expression of. csr1-1D (a. CSR1 mutant) eliminated anther-selective ALS inhibition and reversed the TM-induced male sterile phenotype in both rapeseed and. Arabidopsis. The results of TM daub-stem experiments, combined with the observations of little TM accumulation in anthers and reversion of TM-induced male sterility by targeted expression of the TM metabolism gene. Bel in either the mesophyll or phloem, suggested that foliar-sprayed TM was polar-transported to anthers mainly through the mesophyll and phloem. Microscopy and immunoblotting revealed that autophagy, a bulk degradation process induced during cell death, was elevated in TM-induced male sterile anthers and by anther-specific knockdown of. ALS. Moreover, TM-induced pollen abortion was significantly inhibited by the autophagy inhibitor 3-MA. These data suggested that TM was polar-transported to anthers, resulting in BCAA starvation via anther-specific ALS inhibition and, ultimately, autophagic cell death in anthers. This paper reports that inhibition of ALS activity in anther by TM could cause BCAA starvation, resulting in autophagy in anther cells and leading to male sterility. The results could provide new insights into the mechanism underlying TM-induced male sterility, and have great application potential in crop hybrid seed production.
机译:Tribenuron-methyl(TM)是一种功能强大的磺酰脲类除草剂,可通过靶向乙酰乳酸合酶(ALS)的催化亚基(CSR1)来抑制支链氨基酸(BCAA)的生物合成。通过低剂量叶面喷洒TM选择性诱导雄性不育已广泛用于油菜(甘蓝型油菜)的杂交种子生产。但是,其潜在机制仍然未知。在这里,我们报道了在施用花药后,在花药中比在叶和茎中更大的TM积累以及随后的更强的ALS抑制和BCAA饥饿。组成型或花药特异性的表达。 csr1-1D(a。CSR1突变体)消除了花药对ALS的抑制作用,并逆转了油菜籽和油菜籽中TM诱导的雄性不育表型。拟南芥。 TM涂抹实验的结果,结合观察到的TM在花药中很少的TM积累和通过TM代谢基因的靶向表达逆转TM诱导的雄性不育。叶肉或韧皮部中的Bel表明,叶面喷洒的TM主要通过叶肉和韧皮部极性转移到花药中。显微镜检查和免疫印迹显示,自噬是细胞死亡期间诱导的整体降解过程,在TM诱导的雄性不育花药中和通过其对花药的特异性抑制而升高。 ALS。此外,自噬抑制剂3-MA显着抑制了TM诱导的花粉流产。这些数据表明TM被极性转移到花药中,通过对花药的特异性ALS抑制导致BCAA饥饿,最终导致花药中自噬细胞死亡。本文报道,TM抑制花药中的ALS活性可能导致BCAA饥饿,导致花药细胞自噬并导致雄性不育。该结果可以为TM诱导的雄性不育的潜在机理提供新的见解,并在作物杂交种子生产中具有巨大的应用潜力。

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