Evidence map›Paper›PMID 29546443›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2018

Map-based cloning and characterization of Zea mays male sterility33 (ZmMs33) gene, encoding a glycerol-3-phosphate acyltransferase.

Ke Xie, Suowei Wu, Ziwen Li, Yan Zhou, Danfeng Zhang, Zhenying Dong, Xueli An, Taotao Zhu, Simiao Zhang, Shuangshuang Liu and 2 more

Open access · hybridAbstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 73 citations in OpenAlex.

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  20. International journal of molecular sciences · 2021
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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

12 authors at 2 institutions in 1 country.

Ke XieAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Suowei WuAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.ORCID http://orcid.org/0000-0003-3335-0632
Ziwen LiAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Yan ZhouBeijing Engineering Laboratory of Main Crop Biotechnology Breeding, Beijing Solidwill Sci-Tech Co. Ltd, Beijing, 100192, China.
Danfeng ZhangBeijing Engineering Laboratory of Main Crop Biotechnology Breeding, Beijing Solidwill Sci-Tech Co. Ltd, Beijing, 100192, China.
Zhenying DongAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Xueli AnAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Taotao ZhuAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Simiao ZhangAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China.
Shuangshuang LiuBeijing Engineering Laboratory of Main Crop Biotechnology Breeding, Beijing Solidwill Sci-Tech Co. Ltd, Beijing, 100192, China.
Jinping LiBeijing Engineering Laboratory of Main Crop Biotechnology Breeding, Beijing Solidwill Sci-Tech Co. Ltd, Beijing, 100192, China.
Xiangyuan WanAdvanced Biotechnology and Application Research Center, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100024, China. wanxiangyuan@ustb.edu.cn.ORCID http://orcid.org/0000-0002-5939-4847
University of Science and Technology Beijing · CNInstitute of Crop Sciences · CN

Funding

EPA EP-C-17-009EPA EP-W-17-011the Beijing Science & Technology Plan Program Z161100000916013the Fundamental Research Funds for the Central Universities of China 06500060the Fundamental Research Funds for the Central Universities of China FRF-BR-17-009Athe Fundamental Research Funds for the Central Universities of China FRF-BR-17-010Athe Fundamental Research Funds for the Central Universities of China FRF-BR-17-011Athe International S&T Cooperation Program of China 2015DFA30640the National Key R&D Program of China 2017YFD0101201the National Key R&D Program of China 2017YFD0102001the National Key Technology R&D Program of China 2014BAD01B02the National Natural Science Foundation of China 31771875
6 · The paper itself

Abstract

key messageMap-based cloning of maize ms33 gene showed that ZmMs33 encodes a sn-2 glycerol-3-phosphate acyltransferase, the ortholog of rice OsGPAT3, and it is essential for male fertility in maize. Genetic male sterility has been widely studied for its biological significance and commercial value in hybrid seed production. Although many male-sterile mutants have been identified in maize (Zea mays L.), it is likely that most genes that cause male sterility are unknown. Here, we report a recessive genetic male-sterile mutant, male sterility33 (ms33), which displays small, pale yellow anthers, and complete male sterility. Using a map-based cloning approach, maize GRMZM2G070304 was identified as the ms33 gene (ZmMs33). ZmMs33 encodes a novel sn-2 glycerol-3-phosphate acyltransferase (GPAT) in maize. A functional complementation experiment showed that GRMZM2G070304 can rescue the male-sterile phenotype of the ms33-6029 mutant. GRMZM2G070304 was further confirmed to be the ms33 gene via targeted knockouts induced by the clustered regularly interspersed short palindromic repeats (CRISPR)/Cas9 system. ZmMs33 is preferentially expressed in the immature anther from the quartet to early-vacuolate microspore stages and in root tissues at the fifth leaf growth stage. Phylogenetic analysis indicated that ZmMs33 and OsGPAT3 are evolutionarily conserved for anther and pollen development in monocot species. This study reveals that the monocot-specific GPAT3 protein plays an important role in male fertility in maize, and ZmMs33 and mutants in this gene may have value in maize male-sterile line breeding and hybrid seed production.

Indexed as

Genes, PlantAmino Acid SequenceChromosome MappingCloning, MolecularCRISPR-Cas SystemsGenes, RecessiveGlycerol-3-Phosphate O-AcyltransferasePhenotypePhylogenyPlant InfertilityPlant RootsPollenZea maysGlycerol-3-Phosphate O-Acyltransferase

Identifiers

PMID29546443
PMCPMC5945757
OpenAlexW2792081965

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.