Ontology highlight
ABSTRACT:
SUBMITTER: Sawicki MP
PROVIDER: S-EPMC6656424 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature
Sawicki Mark P MP Gholkar Ankur A AA Torres Jorge Z JZ
Endocrinology 20190801 8
Menin is the protein mutated in patients with multiple endocrine neoplasia type 1 (MEN1) syndrome and their corresponding sporadic tumor counterparts. We have found that menin functions in promoting proper cell division. Here, 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. In our study, menin depletion led to defects in spindle assembly and chromosome congression ...[more]