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番茄中 aconitase 基因家族的全基因组鉴定及其在雄性不育中的 CRISPR 功能表征

Genome-Wide Identification of the Aconitase Gene Family in Tomato () and CRISPR-Based Functional Characterization of on Male-Sterility.

机构信息

Department of Agricultural Biotechnology, Faculty of Agriculture, Ondokuz Mayıs University, 55270 Samsun, Turkey.

Burdur Food Agriculture and Livestock Vocational School, Burdur Mehmet Akif Ersoy University, 15030 Burdur, Turkey.

出版信息

Int J Mol Sci. 2022 Nov 12;23(22):13963. doi: 10.3390/ijms232213963.

Abstract

Tomato () is one of the most cultivated vegetables in the world due to its consumption in a large variety of raw, cooked, or processed foods. Tomato breeding and productivity highly depend on the use of hybrid seeds and their higher yield, environmental adaption, and disease tolerance. However, the emasculation procedure during hybridization raises tomato seed production costs and labor expenses. Using male sterility is an effective way to reduce the cost of hybrid seeds and ensure cultivar purity. Recent developments in CRISPR genome editing technology enabled tomato breeders to investigate the male sterility genes and to develop male-sterile tomato lines. In the current study, the tomato Acotinase () gene family was investigated via in silico tools and functionally characterized with CRISPR/Cas9-mediated gene disruption. Genome-wide blast and HMM search represented two genes located on different tomato chromosomes. Both genes were estimated to have a segmental duplication in the tomato genome due to their identical motif and domain structure. One of these genes, , showed a high expression profile in all generative cells of tomato. Therefore, the gene was targeted with two different gRNA/Cas9 constructs to identify their functional role in tomatoes. The gene was mutated in a total of six genome-edited tomato lines, two of which were homozygous. Surprisingly, pollen viability was found to be extremely low in mutant plants compared to their wild-type (WT) counterparts. Likewise, the number of seeds per fruit also sharply decreased more than fivefold in mutant lines (10-12 seeds) compared to that in WT (67 seeds). The pollen shape, anther structures, and flower colors/shapes were not significantly varied between the mutant and WT tomatoes. The mutated lines were also subjected to salt and mannitol-mediated drought stress to test the effect of on abiotic stress tolerance. The results of the study indicated that mutant tomatoes have higher tolerance with significantly lower MDA content under stress conditions. This is the first CRISPR-mediated characterization of genes on pollen viability, seed formation, and abiotic stress tolerance in tomatoes.

摘要

番茄(Solanum lycopersicum)因其在各种生、熟或加工食品中的广泛消费,成为世界上种植最多的蔬菜之一。番茄的培育和生产力高度依赖于杂交种子的使用,这些种子具有更高的产量、环境适应性和疾病耐受性。然而,在杂交过程中进行的去雄程序会增加番茄种子的生产成本和劳动力费用。利用雄性不育是降低杂交种子成本和确保品种纯度的有效方法。CRISPR 基因组编辑技术的最新进展使番茄育种者能够研究雄性不育基因,并开发雄性不育的番茄品系。在本研究中,通过计算机工具研究了番茄 Acotinase()基因家族,并通过 CRISPR/Cas9 介导的基因敲除对其功能进行了表征。全基因组比对和 HMM 搜索鉴定出两个位于不同番茄染色体上的基因。由于它们具有相同的基序和结构域结构,这两个基因被认为在番茄基因组中发生了片段重复。其中一个基因,,在番茄所有有性生殖细胞中均表现出高表达谱。因此,使用两个不同的 gRNA/Cas9 构建体靶向该基因,以鉴定其在番茄中的功能作用。该基因在总共 6 个经基因组编辑的番茄系中发生突变,其中 2 个为纯合突变。令人惊讶的是,与野生型(WT)相比,突变体植物的花粉活力极低。同样,突变系的每个果实中的种子数量也急剧减少了五倍以上(10-12 粒),而 WT 的种子数量为 67 粒。突变体和 WT 番茄之间的花粉形状、花药结构和花的颜色/形状没有明显差异。突变系还受到盐和甘露醇介导的干旱胁迫处理,以测试 Acotinase 基因对非生物胁迫耐受性的影响。研究结果表明,在胁迫条件下,突变体番茄的 MDA 含量显著降低,具有更高的耐受性。这是首次在番茄中通过 CRISPR 介导的方法对 Acotinase 基因在花粉活力、种子形成和非生物胁迫耐受性方面进行的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bdb/9699144/f478f157c192/ijms-23-13963-g001.jpg

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