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利用花粉特异性基因开关系统对无融合生殖杂交水稻进行高效克隆种子分选

Efficient clonal seeds sorting for apomictic hybrid rice using a pollen-specific gene switch system.

作者信息

Zhan Yijie, Xia Yumei, Wang Yao, Liu Siqing, Zhang XiuLi, Xiong Shuo, Lv Qiming, Cao Mengliang

机构信息

Long Ping Branch, College of Biology, Hunan University, Changsha, China.

State Key Laboratory of Hybrid Rice, Hunan Hybrid Rice Research Center, Changsha, China.

出版信息

Plant Biotechnol J. 2025 Jun;23(6):2266-2275. doi: 10.1111/pbi.70031. Epub 2025 Mar 19.

Abstract

Significant progress in apomictic hybrid rice development faces challenges like achieving high induction rates and seed-setting efficiencies, and distinguishing clonal from zygotic embryos. To address the challenge of selecting clonal seeds, we developed a dual-fluorescence labelling gene switch system using the recombinase Cre/LoxP + FRT. Initially, this system was tested in callus tissue under a constitutive promoter; then, we replaced the promoter with a pollen-specific one to develop the pollen-specific gene switch (PSGS) system. The effectiveness of PSGS in rice pollen was subsequently validated. After confirming its functionality, we co-transformed the PSGS vectors with apomixis vectors in hybrid rice Yongyou 2640 (YE) and Yongyou 4949 (YS) using Agrobacterium-mediated transformation. Finally, we identified 18 MiMe mutants carrying the PSGS; the progeny of 16 lines were all red fluorescence seeds (zygotic embryo). Surprisingly, line L47-4 and L151-1 yielded 418 (n = 418) and 218 (n = 1279) non-fluorescent seeds in the T generation, respectively. The ploidy detection of non-fluorescent seeds showed that 57 (n = 68) and 64 (n = 72) were diploid in Line L47-4 and L151-1, individually. This phenomenon was reproducible in the T generation; 97 (n = 121) and 164 (n = 187) non-fluorescent seeds were diploid from line L47-4 and L151-1, respectively. This study demonstrates the ability of PSGS to distinguish between clonal seeds and zygotic seeds, with a sorting accuracy rate ranging from 80.2% to 88.9%, which is essential for improving clonal seed purity and advancing apomixis in rice cultivation.

摘要

无融合生殖杂交水稻的发展取得了重大进展,但也面临着诸多挑战,如实现高诱导率和结实效率,以及区分克隆胚和合子胚。为应对选择克隆种子的挑战,我们利用重组酶Cre/LoxP + FRT开发了一种双荧光标记基因开关系统。最初,该系统在组成型启动子下的愈伤组织中进行了测试;然后,我们将启动子替换为花粉特异性启动子,以开发花粉特异性基因开关(PSGS)系统。随后验证了PSGS在水稻花粉中的有效性。在确认其功能后,我们使用农杆菌介导的转化方法,将PSGS载体与无融合生殖载体共转化到杂交水稻甬优2640(YE)和甬优4949(YS)中。最后,我们鉴定出18个携带PSGS的MiMe突变体;16个株系的后代均为红色荧光种子(合子胚)。令人惊讶的是,L47 - 4和L151 - 1株系在T代分别产生了418颗(n = 418)和218颗(n = 1279)非荧光种子。对非荧光种子的倍性检测表明,L47 - 4和L151 - 1株系中分别有57颗(n = 68)和64颗(n = 72)为二倍体。这种现象在T代中具有可重复性;L47 - 4和L151 - 1株系分别有97颗(n = 121)和164颗(n = 187)非荧光种子为二倍体。本研究证明了PSGS区分克隆种子和合子种子的能力,分选准确率在80.2%至88.9%之间,这对于提高克隆种子纯度和推进水稻栽培中的无融合生殖至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aea/12120867/93b5bff7161e/PBI-23-2266-g003.jpg

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