Evidence map›Paper›PMID 31159725›Full record

ArticleBMC plant biology2019

Uncovering anthocyanin biosynthesis related microRNAs and their target genes by small RNA and degradome sequencing in tuberous roots of sweetpotato.

Liheng He, Ruimin Tang, Xiaowen Shi, Wenbing Wang, Qinghe Cao, Xiayu Liu, Ting Wang, Yan Sun, Hongmei Zhang, Runzhi Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
10.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 63 citations in OpenAlex.

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  13. Anthocyanin Biosynthesis Genes as Model Genes for Genome Editing in Plants.International journal of molecular sciences · 2021
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  14. Regulatory Mechanisms of Anthocyanin Biosynthesis in Apple and Pear.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Liheng HeShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Ruimin TangShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Xiaowen ShiShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Wenbing WangShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Qinghe CaoJiangsu Xuzhou Sweetpotato Research Center, Xuzhou, 221131, Jiangsu, China.
Xiayu LiuShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Ting WangShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Yan SunShanxi Agriculture University, Taigu, 030801, Shanxi, China.
Hongmei ZhangMaize Research Institute, Shanxi Academy of Agricultural Sciences, Xinzhou, China.
Runzhi LiShanxi Agriculture University, Taigu, 030801, Shanxi, China. rli2001@hotmail.com.
Xiaoyun JiaShanxi Agriculture University, Taigu, 030801, Shanxi, China. gssjxy@hotmail.com.
Shanxi Agricultural University · CNShanxi Academy of Agricultural Sciences · CNSweet Potato Research Institute · CN

Funding

Coal-based Key Sci-Tech Project of Shanxi Province FT-2014-01Key R&D Program of Shanxi Province 201803D221008-6National Key R&D Program of China 2018YFD1000705, 2018YFD1000700National Key Scientific Instrument and Equipment Development Projects of China (CN) SXNGJSKYZX201701-03NSFC 31101555, 31571611NSF of Shanxi Province 201801D121238Science and Technology Innovation Fund of Shanxi Agricultural University 2018yz001
6 · The paper itself

Abstract

backgroundCompared with white-fleshed sweetpotato (WFSP), purple-fleshed sweetpotato (PFSP) is a desirable resource for functional food development because of the abundant anthocyanin accumulation in its tuberous roots. Some studies have shown that the expression regulation mediated by miRNA plays an important role in anthocyanin biosynthesis in plants. However, few miRNAs and their corresponding functions related to anthocyanin biosynthesis in tuberous roots of sweetpotato have been known.

resultsIn this study, small RNA (sRNA) and degradome libraries from the tuberous roots of WFSP (Xushu-18) and PFSP (Xuzishu-3) were constructed, respectively. Totally, 191 known and 33 novel miRNAs were identified by sRNA sequencing, and 180 target genes cleaved by 115 known ib-miRNAs and 5 novel ib-miRNAs were identified by degradome sequencing. Of these, 121 miRNAs were differently expressed between Xushu-18 and Xuzishu-3. Integrated analysis of sRNA, degradome sequencing, GO, KEGG and qRT-PCR revealed that 26 differentially expressed miRNAs and 36 corresponding targets were potentially involved in the anthocyanin biosynthesis. Of which, an inverse correlation between the expression of ib-miR156 and its target ibSPL in WFSP and PFSP was revealed by both qRT-PCR and sRNA sequencing. Subsequently, ib-miR156 was over-expressed in Arabidopsis. Interestingly, the ib-miR156 over-expressing plants showed suppressed abundance of SPL and a purplish phenotype. Concomitantly, upregulated expression of four anthocyanin pathway genes was detected in transgenic Arabidopsis plants. Finally, a putative ib-miRNA-target model involved in anthocyanin biosynthesis in sweetpotato was proposed.

conclusionsThe results represented a comprehensive expression profiling of miRNAs related to anthocyanin accumulation in sweetpotato and provided important clues for understanding the regulatory network of anthocyanin biosynthesis mediated by miRNA in tuberous crops.

Indexed as

Gene Expression Regulation, PlantAnthocyaninsHigh-Throughput Nucleotide SequencingIpomoea batatasMicroRNAsPlant RootsRNA, PlantSequence Analysis, RNAAnthocyaninsMicroRNAsRNA, PlantAnthocyanin biosynthesisDegradome analysisMiR156Small RNA sequencingSweetpotato

Identifiers

PMID31159725
PMCPMC6547535
OpenAlexW2948296394

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.