Menin Associates with the Mitotic Spindle and is Important for Cell Division

メタデータ

公開日
2019-03-18
DOI
  • 10.15146/r32q3j
公開者
Dryad
データ作成者 (e-Rad)
  • Torres, Jorge
  • Sawicki, Mark
  • Gholkar, Ankur

説明

Menin is the protein mutated in patients with multiple endocrine neoplasia type 1 (MEN1) syndrome and their corresponding sporadic tumor counterparts. Here, we have uncovered a novel function for menin in promoting proper cell division. We show that menin localizes to the mitotic spindle poles and the mitotic spindle during early mitosis and to the intercellular bridge microtubules during cytokinesis in HeLa cells. Menin depletion led to defects in spindle assembly and chromosome congression during early mitosis, lagging chromosomes during anaphase, defective cytokinesis, multinucleated interphase cells, and cell death. Additionally, pharmacological inhibition of the menin-MLL1 interaction also led to similar cell division defects. These results indicate that menin and the menin-MLL1 interaction are important for proper cell division. These results highlight a novel function for menin in cell division and aid our understanding of how mutation and misregulation of menin promotes tumorigenesis.

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詳細情報 詳細情報について

  • CRID
    1883116918117748736
  • DOI
    10.15146/r32q3j
  • 本文言語コード
    en
  • データソース種別
    • OpenAIRE
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