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  Computational and genetic reduction of a cell cycle to its simplest, primordial components

Murray, S. M., Panis, G., Fumeaux, C., Viollier, P. H., & Howard, M. (2014). Computational and genetic reduction of a cell cycle to its simplest, primordial components. PLoS Biol, 11(12), e1001749. doi:10.1371/journal.pbio.1001749.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-000B-777A-7 版のパーマリンク: https://hdl.handle.net/21.11116/0000-000B-777C-5
資料種別: 学術論文

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https://www.ncbi.nlm.nih.gov/pubmed/24415923 (全文テキスト(全般))
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 作成者:
Murray, S. M.1, 著者           
Panis, G., 著者
Fumeaux, C., 著者
Viollier, P. H., 著者
Howard, M., 著者
所属:
1Computational and Systems Biology, John Innes Centre, Norwich, United Kingdom, ou_persistent22              

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キーワード: Caulobacter crescentus/*genetics/*physiology Cell Cycle/*genetics/physiology Cell Survival/genetics/physiology Computational Biology/methods Computer Simulation DNA Transposable Elements/genetics/physiology Gene Expression Regulation, Bacterial/genetics/physiology Methylation Models, Biological
 要旨: What are the minimal requirements to sustain an asymmetric cell cycle? Here we use mathematical modelling and forward genetics to reduce an asymmetric cell cycle to its simplest, primordial components. In the Alphaproteobacterium Caulobacter crescentus, cell cycle progression is believed to be controlled by a cyclical genetic circuit comprising four essential master regulators. Unexpectedly, our in silico modelling predicted that one of these regulators, GcrA, is in fact dispensable. We confirmed this experimentally, finding that DeltagcrA cells are viable, but slow-growing and elongated, with the latter mostly due to an insufficiency of a key cell division protein. Furthermore, suppressor analysis showed that another cell cycle regulator, the methyltransferase CcrM, is similarly dispensable with simultaneous gcrA/ccrM disruption ameliorating the cytokinetic and growth defect of DeltagcrA cells. Within the Alphaproteobacteria, gcrA and ccrM are consistently present or absent together, rather than either gene being present alone, suggesting that gcrA/ccrM constitutes an independent, dispensable genetic module. Together our approaches unveil the essential elements of a primordial asymmetric cell cycle that should help illuminate more complex cell cycles.

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 日付: 2014-01-15
 出版の状態: 出版
 ページ: -
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 査読: -
 識別子(DOI, ISBNなど): その他: 24415923
DOI: 10.1371/journal.pbio.1001749
ISSN: 1545-7885 (Electronic)1544-9173 (Linking)
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出版物 1

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出版物名: PLoS Biol
種別: 学術雑誌
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出版社, 出版地: -
ページ: - 巻号: 11 (12) 通巻号: - 開始・終了ページ: e1001749 識別子(ISBN, ISSN, DOIなど): -