4.8 Article

Nuclear membrane protein Lem2 regulates nuclear size through membrane flow

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-09623-x

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资金

  1. Francis Crick Institute from Cancer Research UK [FC01121]
  2. UK Medical Research Council [FC01121]
  3. Wellcome Trust [FC01121, 093917]
  4. JSPS KAKENHI [JP26660089, 17K07756]
  5. JSPS [S2902]
  6. Hiroshima University Education and Research Support Foundation
  7. Breast Cancer Research Foundation
  8. Lord Leonard and Lady Estelle Wolfson Foundation
  9. Grants-in-Aid for Scientific Research [17K07756] Funding Source: KAKEN

向作者/读者索取更多资源

The size of the membrane-bound nucleus scales with cell size in a wide range of cell types but the mechanisms determining overall nuclear size remain largely unknown. Here we investigate the role of fission yeast inner nuclear membrane proteins in determining nuclear size, and propose that the Lap2-Emerin-Manl domain protein Lem2 acts as a barrier to membrane flow between the nucleus and other parts of the cellular membrane system. Lem2 deletion increases membrane flow into and out of the nuclear envelope in response to changes in membrane synthesis and nucleocytoplasmic transport, altering nuclear size. The endoplasmic reticulum protein Lnp1 acts as a secondary barrier to membrane flow, functionally compensating for lack of Lem2. We propose that this is part of the mechanism that maintains nuclear size proportional to cellular membrane content and thus to cell size. Similar regulatory principles may apply to other organelles in the eukaryotic subcellular membrane network.

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