Evidence map›Paper›PMID 30598106›Full record

ArticleBMC genomics2018

Genotype- and tissue-specific miRNA profiles and their targets in three alfalfa (Medicago sativa L) genotypes.

Robert Pokoo, Shuchao Ren, Qingyi Wang, Christy M Motes, Timothy D Hernandez, Sayvan Ahmadi, Maria J Monteros, Yun Zheng, Ramanjulu Sunkar

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

14 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Robert PokooDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, 74078, USA.
Shuchao RenInstitute of Primate Translational Medicine, Kunming University of Science and Technology, 727 South Jingming Road, Kunming, 650500, Yunnan, China.
Qingyi WangInstitute of Primate Translational Medicine, Kunming University of Science and Technology, 727 South Jingming Road, Kunming, 650500, Yunnan, China.
Christy M MotesNoble Research Institute, Ardmore, OK, 73401, USA.
Timothy D HernandezNoble Research Institute, Ardmore, OK, 73401, USA.
Sayvan AhmadiDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, 74078, USA.
Maria J MonterosNoble Research Institute, Ardmore, OK, 73401, USA.
Yun ZhengInstitute of Primate Translational Medicine, Kunming University of Science and Technology, 727 South Jingming Road, Kunming, 650500, Yunnan, China. zhengyun5488@gmail.com.
Ramanjulu SunkarDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, 74078, USA. ramanjulu.sunkar@okstate.edu.
Kunming University of Science and Technology · CNNoble Research Institute · USOklahoma State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlfalfa (Medicago sativa L.) is a forage legume with significant agricultural value worldwide. MicroRNAs (miRNAs) are key components of post-transcriptional gene regulation and essentially regulate many aspects of plant growth and development. Although miRNAs were reported in alfalfa, their expression profiles in different tissues and the discovery of novel miRNAs as well as their targets have not been described in this plant species.

resultsTo identify tissue-specific miRNA profiles in whole plants, shoots and roots of three different alfalfa genotypes (Altet-4, NECS-141and NF08ALF06) were used. Small RNA libraries were generated and sequenced using a high-throughput sequencing platform. Analysis of these libraries enabled identification of100 miRNA families; 21 of them belong to the highly conserved families while the remaining 79 families are conserved at the minimum between M. sativa and the model legume and close relative, M. truncatula. The profiles of the six abundantly expressed miRNA families (miR156, miR159, miR166, miR319, miR396 and miR398) were relatively similar between the whole plants, roots and shoots of these three alfalfa genotypes. In contrast, robust differences between shoots and roots for miR160 and miR408 levels were evident, and their expression was more abundant in the shoots. Additionally, 17 novel miRNAs were identified and the relative abundance of some of these differed between tissue types. Further, the generation and analysis of degradome libraries from the three alfalfa genotypes enabled confirmation of 69 genes as targets for 31 miRNA families in alfalfa.

conclusionsThe miRNA profiles revealed both similarities and differences in the expression profiles between tissues within a genotype as well as between the genotypes. Among the highly conserved miRNA families, miR166 was the most abundantly expressed in almost all tissues from the three genotypes. The identification of conserved and novel miRNAs as well as their targets in different tissues of multiple genotypes increased our understanding of miRNA-mediated gene regulation in alfalfa and could provide valuable insights for practical research and plant improvement applications in alfalfa and related legume species.

Indexed as

GenotypeBase SequenceGene Expression ProfilingGene LibraryGenetic VariationMedicago sativaMicroRNAsMolecular Sequence AnnotationOrgan SpecificityRNA, PlantMicroRNAsRNA, Plant

Identifiers

PMID30598106
PMCPMC6311939
OpenAlexW2908248290

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LicenceCC BY
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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.