Evidence map›Paper›PMID 26728635›Full record

ArticleBMC genomics2016

Transcriptome analysis of secondary cell wall development in Medicago truncatula.

Huanzhong Wang, Jung Hyun Yang, Fang Chen, Ivone Torres-Jerez, Yuhong Tang, Mingyi Wang, Qian Du, Xiaofei Cheng, Jiangqi Wen, Richard Dixon

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.5field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Characterization, Expression Profiling, and Biochemical Analyses of theInternational journal of molecular sciences · 2022
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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

10 authors at 2 institutions in 1 country.

Huanzhong WangDepartment of Plant Science and Landscape Architecture, University of Connecticut, 1390 Storrs Rd., Storrs, CT, 06269, USA. huanzhong.wang@uconn.edu.
Jung Hyun YangDepartment of Plant Science and Landscape Architecture, University of Connecticut, 1390 Storrs Rd., Storrs, CT, 06269, USA. jung.yang@uconn.edu.
Fang ChenPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. Fang.Chen@unt.edu.
Ivone Torres-JerezPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. itjerez@noble.org.
Yuhong TangPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. ytang@noble.org.
Mingyi WangPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. mingy.wang@gmail.com.
Qian DuDepartment of Plant Science and Landscape Architecture, University of Connecticut, 1390 Storrs Rd., Storrs, CT, 06269, USA. qian.du@uconn.edu.
Xiaofei ChengPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. xcheng@noble.org.
Jiangqi WenPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. jwen@noble.org.
Richard DixonPlant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA. Richard.Dixon@unt.edu.
Noble Research Institute · USUniversity of Connecticut · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLegumes are important to humans by providing food, feed and raw materials for industrial utilizations. Some legumes, such as alfalfa, are potential bioenergy crops due to their high biomass productivity. Global transcriptional profiling has been successfully used to identify genes and regulatory pathways in secondary cell wall thickening in Arabidopsis, but such transcriptome data is lacking in legumes.

resultsA systematic microarray assay and high through-put real time PCR analysis of secondary cell wall development were performed along stem maturation in Medicago truncatula. More than 11,000 genes were differentially expressed during stem maturation, and were categorized into 10 expression clusters. Among these, 279 transcription factor genes were correlated with lignin/cellulose biosynthesis, therefore representing putative regulators of secondary wall development. The b-ZIP, NAC, WRKY, C2H2 zinc finger (ZF), homeobox, and HSF gene families were over-represented. Gene co-expression network analysis was employed to identify transcription factors that may regulate the biosynthesis of lignin, cellulose and hemicellulose. As a complementary approach to microarray, real-time PCR analysis was used to characterize the expression of 1,045 transcription factors in the stem samples, and 64 of these were upregulated more than 5-fold during stem maturation. Reverse genetics characterization of a cellulose synthase gene in cluster 10 confirmed its function in xylem development.

conclusionsThis study provides a useful transcriptome and expression resource for understanding cell wall development, which is pivotal to enhance biomass production in legumes.

Indexed as

Gene Expression ProfilingCell WallGene Expression Regulation, PlantGene Regulatory NetworksGlucosyltransferasesLigninMedicago truncatulaPlant StemsTranscription Factorscellulose synthaseGlucosyltransferasesLigninTranscription Factors

Identifiers

PMID26728635
PMCPMC4700669
OpenAlexW2231222660

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.