Evidence map›Paper›PMID 23070302›Full record

ArticlePlant cell reports2013

Genetic mapping and isolation of two arc3 alleles in Arabidopsis.

Deng Pan, Yuhong Shi, Xia Liu, Yuefang Gao, Zhonghua Liu, Hongbo Gao

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Article in Plant cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

  1. Structural and functional insights into the chloroplast division site regulators PARC6 and PDV1 in the intermembrane space.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  2. Frontiers in plant science · 2017
    Article
  3. Article
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5 · Who and what money

Authors and funding

6 authors.

Deng PanCollege of Biological Sciences and Biotechnology, Beijing Forestry University, Haidian, Beijing, 100083, China.
Yuhong Shi
Xia Liu
Yuefang Gao
Zhonghua Liu
Hongbo Gao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key messageTwo new alleles of arc3 in Arabidopsis thaliana, arc3-4 and arc3-5, were isolated in the Columbia-0 ecotype. The mutants were characterized in detail using microscopy and molecular techniques. Chloroplasts are essential organelles for photosynthesis in plant cells. Division of chloroplasts is coordinated by the internal division machinery (mainly the tubulin-like FtsZ ring) and the external division machinery (mainly the dynamin-like ARC5 ring). Accumulation and replication of chloroplasts3 (ARC3) is important for the correct positioning of chloroplast division machinery. During evolution, ARC3 has probably replaced minicellC (MinC), an important factor involved in positioning of the division site in bacteria. However, the working mechanism of ARC3 is still unclear. Using forward genetic approaches, we isolated two new alleles of arc3 in Arabidopsis thaliana, arc3-4 and arc3-5, in which mutant loci differed from those of previously reported arc3 mutants. Microscopy analyses showed more detailed, and some new, phenotypes of arc3 mutants. Reverse-transcription polymerase chain reaction (RT-PCR) and real-time quantitative RT-PCR (qRT-PCR) results indicated that the mRNA of the ARC3 gene was unstable in arc3-4 and arc3-5 mutant plants. Also, RNA secondary structures of the ARC3 gene were predicted to differ between these two arc3 mutants and wild type. Our studies increase our understanding of the function of ARC3 in chloroplast division.

Indexed as

AllelesChromosome MappingAmino Acid SequenceArabidopsisArabidopsis ProteinsBase SequenceChloroplastsChromosome SegregationCrosses, GeneticGene Expression Regulation, PlantGenetic MarkersMesophyll CellsMolecular Sequence DataMutationNucleic Acid ConformationPhenotypeArabidopsis ProteinsARC3 protein, ArabidopsisGenetic MarkersRNA, Messenger

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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.