Regulatory loops between rice transcription factors OsNAC25 and OsNAC20/26 balance starch synthesis

淀粉 胚乳 转录因子 生物 调节器 调节基因 基因 细胞生物学 水稻 突变体 基因表达调控 生物化学
作者
Juan Wang,Haiqin Zhang,Yuanjiang Wang,Shanshan Meng,Qing Liu,Qian Li,Zhongbo Zhao,Qiaoquan Liu,Cunxu Wei
出处
期刊:Plant Physiology [Oxford University Press]
卷期号:195 (2): 1365-1381 被引量:2
标识
DOI:10.1093/plphys/kiae139
摘要

Abstract Several starch synthesis regulators have been identified, but these regulators are situated in the terminus of the regulatory network. Their upstream regulators and the complex regulatory network formed between these regulators remain largely unknown. A previous study demonstrated that NAM, ATAF, and CUC (NAC) transcription factors, OsNAC20 and OsNAC26 (OsNAC20/26), redundantly and positively regulate the accumulation of storage material in rice (Oryza sativa) endosperm. In this study, we detected OsNAC25 as an upstream regulator and interacting protein of OsNAC20/26. Both OsNAC25 mutation and OE resulted in a chalky seed phenotype, decreased starch content, and reduced expression of starch synthesis–related genes, but the mechanisms were different. In the osnac25 mutant, decreased expression of OsNAC20/26 resulted in reduced starch synthesis; however, in OsNAC25-overexpressing plants, the OsNAC25–OsNAC20/26 complex inhibited OsNAC20/26 binding to the promoter of starch synthesis–related genes. In addition, OsNAC20/26 positively regulated OsNAC25. Therefore, the mutual regulation between OsNAC25 and OsNAC20/26 forms a positive regulatory loop to stimulate the expression of starch synthesis–related genes and meet the great demand for starch accumulation in the grain filling stage. Simultaneously, a negative regulatory loop forms among the 3 proteins to avoid the excessive expression of starch synthesis–related genes. Collectively, our findings demonstrate that both promotion and inhibition mechanisms between OsNAC25 and OsNAC20/26 are essential for maintaining stable expression of starch synthesis–related genes and normal starch accumulation.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
曾泳钧完成签到,获得积分10
刚刚
1秒前
tianzhen发布了新的文献求助10
1秒前
正直水池完成签到 ,获得积分10
2秒前
简单发布了新的文献求助10
2秒前
Tera完成签到,获得积分10
2秒前
学术瘤子完成签到,获得积分10
3秒前
Hello应助sivan采纳,获得10
3秒前
3秒前
刨地的土拨鼠完成签到,获得积分10
3秒前
3秒前
feezy发布了新的文献求助10
3秒前
4秒前
4秒前
4秒前
4秒前
飞快的尔云完成签到,获得积分20
5秒前
5秒前
领导范儿应助塔塔采纳,获得10
6秒前
6秒前
tyj完成签到,获得积分10
6秒前
JAYZHANG发布了新的文献求助10
7秒前
7秒前
leilei发布了新的文献求助10
7秒前
陈效率完成签到 ,获得积分10
7秒前
柯ke发布了新的文献求助10
8秒前
8秒前
8秒前
完美世界应助干净冰露采纳,获得10
9秒前
CodeCraft应助起个名字真难采纳,获得10
9秒前
orixero应助爱学习采纳,获得10
9秒前
请不要喊我回答问题完成签到 ,获得积分10
9秒前
9秒前
忧心的行云应助敬老院N号采纳,获得10
9秒前
忧心的行云应助敬老院N号采纳,获得10
9秒前
忧心的行云应助敬老院N号采纳,获得10
9秒前
张乐完成签到,获得积分10
10秒前
徐新雨发布了新的文献求助10
10秒前
dingcy0731给dingcy0731的求助进行了留言
10秒前
11秒前
高分求助中
Impact of Mitophagy-Related Genes on the Diagnosis and Development of Esophageal Squamous Cell Carcinoma via Single-Cell RNA-seq Analysis and Machine Learning Algorithms 2000
Evolution 1100
How to Create Beauty: De Lairesse on the Theory and Practice of Making Art 1000
Research Methods for Sports Studies 1000
Gerard de Lairesse : an artist between stage and studio 670
Assessment of Ultrasonographic Measurement of Inferior Vena Cava Collapsibility Index in The Prediction of Hypotension Associated with Tourniquet Release in Total Knee Replacement Surgeries under Spinal Anesthesia 500
T/CAB 0344-2024 重组人源化胶原蛋白内毒素去除方法 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 内科学 物理 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2980887
求助须知:如何正确求助?哪些是违规求助? 2642209
关于积分的说明 7128884
捐赠科研通 2275090
什么是DOI,文献DOI怎么找? 1206860
版权声明 592045
科研通“疑难数据库(出版商)”最低求助积分说明 589646