Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2009 Nov 17;5:328. doi: 10.1038/msb.2009.78

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2009, EMBO and Nature Publishing Group

This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits distribution and reproduction in any medium, provided the original author and source are credited. Creation of derivative works is permitted but the resulting work may be distributed only under the same or similar licence to this one. This licence does not permit commercial exploitation without specific permission.

PMC Copyright notice

Persistent Clb2 after mitotic exit eliminates G1 mating factor sensitivity. A bar1Δ strain (BD127b-9D) was released from cdc20 arrest into α-factor-containing medium (A) without or with (B) a Clb2kd–YFP pulse. Merged YFP, mCherry, and DIC channels are shown. Unbudded cells (black), complete (red) or partial (blue) cytokinesis, and rebudding (green) are plotted versus time post-release for unpulsed cells (A) or versus Clb2kd–YFP concentration 60-min post-release for pulsed cells (B). (C) Cells bearing Myo1–mCherry and GFP fused to the Cln2 degron under the control of the CLN2 promoter (BD143a-21C) were released from cdc20 arrest into α-factor-containing medium with or without a pulse of untagged Clb2kd. Merged GFP, mCherry and DIC channels are shown at 0 and 75 min post-release.