The interphase microtubule damage checkpoint defines an S-phase commitment point and does not require p21(waf-1).

Abstract:

:Cell cycle checkpoints ensure orderly progression of events during cell division. A microtubule damage (MTD)-induced checkpoint has been described in G(1) phase of the cell cycle (G(1)MTC) for which little is known. The present study shows that the G(1)MTC is intact in activated T lymphocytes from mice with the p21(waf-1) gene deleted. However, p21(waf-1) gene deletion does affect the ratio of cells that arrest at the G(1)MTC and the spindle checkpoint after MTD. The G(1)MTC arrests T lymphocytes in G(1) prior to cdc2 up-regulation and prior to G(1) arrest by p21(waf-1). Once cells have progressed past the G(1)MTC, they are committed to chromosome replication and metaphase progression, even with extreme MTD. The G(1)MTC is also present in a human myeloid cell line deficient in p21(waf-1) gene expression. The p21-independent G(1)MTC may be important in cellular responses to MTD such as those induced by drugs used to treat cancer.

journal_name

Blood

journal_title

Blood

authors

Mantel CR,Braun SE,Lee Y,Kim YJ,Broxmeyer HE

doi

10.1182/blood.v97.5.1505

subject

Has Abstract

pub_date

2001-03-01 00:00:00

pages

1505-7

issue

5

eissn

0006-4971

issn

1528-0020

journal_volume

97

pub_type

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