Methyltransferase 1 (OsMTS1) interacts with hydroxycinnamoyltransferase 1 (OsHCT1) and promotes heading by upregulating heading date 1 (Hd1)

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Plant Science Pub Date : 2024-10-15 DOI:10.1016/j.plantsci.2024.112291
Amir Sohail
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Abstract

Heading date determines the distribution and yield potentials of rice, and is an ideal target for crop improvement using CRISPR/Cas9 genome editing system. In this study, we reported the loss-of-function of Methyltransferase 1 (MTS1), which promotes heading in rice. Here, we constructed knockouts and overexpression transgenic plants of OsMTS1 in ZH8015 and Nipponbare (NIP) for the first time to validate its heading date function in rice subspecies Oryza sativa ssp. Indica and O. Sativa ssp. Japonica, respectively. The OsMTS1 knockouts in ZH8015 and NIP rice significantly promoted heading date under both natural short days (NSD) and natural long days (NLD) conditions, while the overexpression of OsMTS1 significantly delayed heading date in ZH8015 and NIP rice under both NSD and NLD conditions. Likewise, the complementation transgenic plants displayed late heading date phenotype. OsMTS1 repressed heading through up-regulating Heading date 1 (Hd1) and down-regulating Early heading date 1 (Ehd1) and Heading date 3a (Hd3a). The OsMTS1 protein interacted with OsHCT1 proteins using a yeast two-hybrid (Y2H) assay. The Y2H and overexpression confirmed that OsMTS1 interacted with OsHCT1, which delayed heading by 4.7 days under NLD. Taken together, CRISPR/Cas9, genetic complementation, and overexpression results validated that OsMTS1 represses heading in Indica and Japonica rice under both NLD and NSD conditions. These results demonstrated that OsMTS1 is a useful target for breeding early maturing rice varieties by CRISPR/Cas9 gene editing of the functional allele.
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甲基转移酶 1(OsMTS1)与羟基肉桂酰基转移酶 1(OsHCT1)相互作用,通过上调标题日期 1(Hd1)促进标题。
抽穗期决定了水稻的分布和产量潜力,是利用 CRISPR/Cas9 基因组编辑系统改良作物的理想目标。在这项研究中,我们报道了促进水稻抽穗的甲基转移酶 1(MTS1)的功能缺失。在此,我们首次在 ZH8015 和 Nipponbare(NIP)中构建了 OsMTS1 基因敲除和过表达转基因植株,以验证其在水稻亚种 Oryza sativa ssp.在自然短日(NSD)和自然长日(NLD)条件下,ZH8015和NIP水稻中敲除的OsMTS1都能显著促进头穗的形成;而在自然短日和自然长日条件下,OsMTS1的过表达都能显著推迟ZH8015和NIP水稻的头穗形成。同样,互补转基因植株也表现出迟发性表型。OsMTS1 通过上调标题日期 1(Hd1)、下调早期标题日期 1(Ehd1)和标题日期 3a(Hd3a)来抑制标题。利用酵母双杂交(Y2H)试验,OsMTS1 蛋白与 OsHCT1 蛋白相互作用。Y2H和过表达证实了OsMTS1与OsHCT1的相互作用,在NLD条件下,OsMTS1可使头状花序延迟4.7天。综上所述,CRISPR/Cas9、基因互补和过表达结果验证了 OsMTS1 在 NLD 和 NSD 条件下均抑制籼稻和粳稻的头状生长。这些结果表明,通过 CRISPR/Cas9 基因编辑功能等位基因,OsMTS1 是培育早熟水稻品种的有用靶标。
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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