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[Cancer Research 59, 5097-5101, October 1, 1999]
© 1999 American Association for Cancer Research

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[Cancer Research 59, 5097-5101, October 15, 1999]
© 1999 American Association for Cancer Research


Advances in Brief

Cell Cycle Regulation of Menin Expression1

Hiroshi Kaji, Lucie Canaff, David Goltzman and Geoffrey N. Hendy2

Departments of Medicine [H. K., L. C., D. G., G. N. H.], Physiology [D. G., G. N. H.], and Human Genetics [G. N. H.], McGill University, Montreal, Quebec, H3A 1A1 Canada

The multiple endocrine neoplasia type 1 gene product, menin, interacts with Jun D. The physiological role of menin in cell cycle control and the manner in which its inactivation contributes to tumorigenesis remain unknown. In the present study, the expression of menin was examined at various cell cycle stages in GH4C1 cells, a rat pituitary cell line. Cells synchronized at the G1-S-phase boundary expressed menin at a lower level than G0-G1-synchronized cells. The expression of menin increased as the cells entered S phase, at which time Jun D expression also increased. In contrast, cells synchronized at the G2-M phase expressed lower levels of menin. At G0-G1, G1-S, and G2-M phases of the cell cycle, menin was found predominantly in the nucleus. In summary, we show that in pituitary cells, menin is a nuclear protein whose expression is cell-cycle regulated. The data suggest that menin has an important role in cell growth regulation.




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Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 1999 by the American Association for Cancer Research.