Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
Institute of Plant Science and Resources, Okayama University, Kurashiki, Japan.
Plant Cell Physiol. 2019 Mar 1;60(3):503-515. doi: 10.1093/pcp/pcz014.
Grain size is a key determiner of grain weight, one of the yield components in rice (Oryza sativa). Therefore, to increase grain yield, it is important to elucidate the detailed mechanisms regulating grain size. The Large grain (Lgg) mutant, found in the nonautonomous DNA-based active rice transposon1 (nDart1)-tagged lines of Koshihikari, is caused by a truncated nDart1-3 and 355 bp deletion in the 5' untranslated region of LGG, which encodes a putative RNA-binding protein, through transposon display and cosegregation analysis between grain length and LGG genotype in F2 and F3. Clustered regularly interspaced short palindromic repeats/CRISPR-associated 9-mediated knockout and overexpression of LGG led to longer and shorter grains than wild type, respectively, showing that LGG regulates spikelet hull length. Expression of LGG was highest in the 0.6-mm-long young panicle and gradually decreased as the panicle elongated. LGG was also expressed in roots and leaves. These results show that LGG functions at the very early stage of panicle development. Longitudinal cell numbers of spikelet hulls of Lgg, knockout and overexpressed plants were significantly different from those of the wild type, suggesting that LGG might regulate longitudinal cell proliferation in the spikelet hull. RNA-Seq analysis of 1-mm-long young panicles from LGG knockout and overexpressing plants revealed that the expressions of many cell cycle-related genes were reduced in knockout plants relative to LGG-overexpressing plants and wild type, whereas some genes for cell proliferation were highly expressed in knockout plants. Taken together, these results suggest that LGG might be a regulator of cell cycle and cell division in the rice spikelet hull.
粒型是决定粒重的关键因素之一,粒重是水稻(Oryza sativa)产量的组成部分之一。因此,要提高稻谷产量,阐明调控粒型的详细机制非常重要。在非自主 DNA 活性水稻转座子 1(nDart1)标记的 lines of Koshihikari 中发现的大粒(Lgg)突变体,是由于 nDart1-3 和 5'非翻译区的 355 bp 缺失导致的截断 LGG,该区域编码一个假定的 RNA 结合蛋白,通过转座子显示和 F2 和 F3 中粒长和 LGG 基因型之间的共分离分析。CRISPR 相关 9 介导的 LGG 敲除和过表达导致穗壳长度比野生型更长和更短,分别表明 LGG 调节小穗壳长度。LGG 在 0.6mm 长的幼穗中表达量最高,随着穗的伸长逐渐降低。LGG 也在根和叶中表达。这些结果表明 LGG 在穗发育的早期阶段发挥作用。Lgg、敲除和过表达植物的小穗壳纵向细胞数与野生型明显不同,表明 LGG 可能调节小穗壳的纵向细胞增殖。LGG 敲除和过表达植物 1mm 长幼穗的 RNA-Seq 分析表明,与 LGG 过表达植物和野生型相比,敲除植物中许多与细胞周期相关的基因表达降低,而一些细胞增殖基因在敲除植物中高度表达。综上所述,这些结果表明 LGG 可能是水稻小穗壳细胞周期和细胞分裂的调节剂。