High-Throughput Sequencing of Small RNA Transcriptomes in Maize Kernel Identifies miRNAs Involved in Embryo and Endosperm Development

胚乳 生物 小RNA 转录组 胚胎 基因 小RNA 遗传学 基因表达 转录因子 基因表达调控 计算生物学
作者
Lijuan Xing,Ming Zhu,Min Zhang,Wenzong Li,Haiyang Jiang,Junjie Zou,Lei Wang,Miaoyun Xu
出处
期刊:Genes [MDPI AG]
卷期号:8 (12): 385-385 被引量:16
标识
DOI:10.3390/genes8120385
摘要

Maize kernel development is a complex biological process that involves the temporal and spatial expression of many genes and fine gene regulation at a transcriptional and post-transcriptional level, and microRNAs (miRNAs) play vital roles during this process. To gain insight into miRNA-mediated regulation of maize kernel development, a deep-sequencing technique was used to investigate the dynamic expression of miRNAs in the embryo and endosperm at three developmental stages in B73. By miRNA transcriptomic analysis, we characterized 132 known miRNAs and six novel miRNAs in developing maize kernel, among which, 15 and 14 miRNAs were commonly differentially expressed between the embryo and endosperm at 9 days after pollination (DAP), 15 DAP and 20 DAP respectively. Conserved miRNA families such as miR159, miR160, miR166, miR390, miR319, miR528 and miR529 were highly expressed in developing embryos; miR164, miR171, miR393 and miR2118 were highly expressed in developing endosperm. Genes targeted by those highly expressed miRNAs were found to be largely related to a regulation category, including the transcription, macromolecule biosynthetic and metabolic process in the embryo as well as the vitamin biosynthetic and metabolic process in the endosperm. Quantitative reverse transcription-PCR (qRT-PCR) analysis showed that these miRNAs displayed a negative correlation with the levels of their corresponding target genes. Importantly, our findings revealed that members of the miR169 family were highly and dynamically expressed in the developing kernel, which will help to exploit new players functioning in maize kernel development.
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
平常从蓉发布了新的文献求助20
刚刚
Xingliang_Wu98完成签到,获得积分10
刚刚
DezhaoWang完成签到,获得积分10
1秒前
如泣草芥完成签到,获得积分0
1秒前
Dlan完成签到,获得积分10
2秒前
zzz完成签到,获得积分10
3秒前
丁小只完成签到,获得积分10
4秒前
dola完成签到,获得积分10
4秒前
overThat发布了新的文献求助10
4秒前
爱科研完成签到,获得积分10
5秒前
hhxx关注了科研通微信公众号
6秒前
Yooki完成签到,获得积分10
8秒前
少一点丶天分完成签到,获得积分10
8秒前
季生发布了新的文献求助10
9秒前
啊啊啊完成签到 ,获得积分10
9秒前
文静醉易完成签到,获得积分10
10秒前
踏实手套完成签到 ,获得积分0
10秒前
Till完成签到 ,获得积分10
12秒前
小可爱完成签到,获得积分10
14秒前
威武的未来完成签到,获得积分10
14秒前
电闪完成签到,获得积分10
14秒前
顺风顺水顺财神完成签到 ,获得积分10
16秒前
16秒前
CipherSage应助慧慧采纳,获得10
18秒前
ktw完成签到,获得积分10
19秒前
111完成签到 ,获得积分10
20秒前
overThat发布了新的文献求助10
20秒前
hujun完成签到 ,获得积分10
21秒前
24秒前
24秒前
平常从蓉发布了新的文献求助20
25秒前
李健的小迷弟应助自由人采纳,获得10
25秒前
昏睡的白桃完成签到,获得积分10
25秒前
hardworkcd完成签到,获得积分20
26秒前
Pluto完成签到 ,获得积分10
26秒前
xiaxia完成签到 ,获得积分10
26秒前
Sherwin完成签到,获得积分10
27秒前
面包完成签到,获得积分10
28秒前
木木198022完成签到,获得积分10
28秒前
小嘴巴发布了新的文献求助10
28秒前
高分求助中
The ACS Guide to Scholarly Communication 2500
Sustainability in Tides Chemistry 2000
Pharmacogenomics: Applications to Patient Care, Third Edition 1000
Studien zur Ideengeschichte der Gesetzgebung 1000
TM 5-855-1(Fundamentals of protective design for conventional weapons) 1000
Threaded Harmony: A Sustainable Approach to Fashion 810
Genera Insectorum: Mantodea, Fam. Mantidæ, Subfam. Hymenopodinæ (Classic Reprint) 800
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 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3085495
求助须知:如何正确求助?哪些是违规求助? 2738341
关于积分的说明 7549285
捐赠科研通 2388102
什么是DOI,文献DOI怎么找? 1266315
科研通“疑难数据库(出版商)”最低求助积分说明 613390
版权声明 598591