Evidence map›Paper›PMID 15604686›Full record

ArticlePlant molecular biology2004

Functional genomic analysis of Arabidopsis thaliana glycoside hydrolase family 1.

Zhiwei Xu, Luis Escamilla-Treviño, Lihui Zeng, Mallikarjun Lalgondar, David Bevan, Brenda Winkel, Ali Mohamed, Chi-Lien Cheng, Ming-Che Shih, Jonathan Poulton and 1 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Plant molecular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 1 pooled it
12.8field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 1 synthesis or guideline pooled it, 342 citations in OpenAlex.

  1. BioprospectingFrontiers in fungal biology · 2021
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  6. The CiWOX13-CiWOX14 Complex RegulatesPlants (Basel, Switzerland) · 2026
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  15. Unlocking saponin biosynthesis in soapwort.Nature chemical biology · 2025
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52 more citing papers are in PubMed but not listed here.

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

11 authors at 4 institutions in 2 countries.

Zhiwei XuDepartment of Biological Sciences, The University of Iowa, Iowa 52242, USA.
Luis Escamilla-Treviño
Lihui Zeng
Mallikarjun Lalgondar
David Bevan
Brenda Winkel
Ali Mohamed
Chi-Lien Cheng
Ming-Che Shih
Jonathan Poulton
Asim Esen
University of Iowa · USVirginia Tech · USFujian Agriculture and Forestry University · CNVirginia State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In plants, Glycoside Hydrolase (GH) Family 1 beta -glycosidases are believed to play important roles in many diverse processes including chemical defense against herbivory, lignification, hydrolysis of cell wall-derived oligosaccharides during germination, and control of active phytohormone levels. Completion of the Arabidopsis thaliana genome sequencing project has enabled us, for the first time, to determine the total number of Family 1 members in a higher plant. Reiterative database searches revealed a multigene family of 48 members that includes eight probable pseudogenes. Manual reannotation and analysis of the entire family were undertaken to rectify existing misannotations and identify phylogenetic relationships among family members. Forty-seven members (designated BGLU1 through BGLU47 ) share a common evolutionary origin and were subdivided into approximately 10 subfamilies based on phylogenetic analysis and consideration of intron-exon organizations. The forty-eighth member of this family ( At3g06510; sfr2 ) is a beta -glucosidase-like gene that belongs to a distinct lineage. Information pertaining to expression patterns and potential functions of Arabidopsis GH Family 1 members is presented. To determine the biological function of all family members, we intend to investigate the substrate specificity of each mature hydrolase after its heterologous expression in the Pichia pastoris expression system. To test the validity of this approach, the BGLU44 -encoded hydrolase was expressed in P. pastoris and purified to homogeneity. When tested against a wide range of natural and synthetic substrates, this enzyme showed a preference for beta -mannosides including 1,4- beta -D-mannooligosaccharides, suggesting that it may be involved in A. thaliana in degradation of mannans, galactomannans, or glucogalactomannans. Supporting this notion, BGLU44 shared high sequence identity and similar gene organization with tomato endosperm beta -mannosidase and barley seed beta -glucosidase/ beta -mannosidase BGQ60.

Indexed as

Genome, PlantArabidopsisArabidopsis ProteinsChromosomes, PlantDatabases, Nucleic AcidEvolution, MolecularExonsGenes, PlantGlycoside HydrolasesIntronsMultigene FamilyPhylogenyRecombinant ProteinsSubstrate SpecificityArabidopsis ProteinsGlycoside HydrolasesRecombinant Proteins

Identifiers

PMID15604686
OpenAlexW2073505705

What OpenQuestion holds

Textmetadata
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.