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First published online February 4, 2009


Journal of Cell Science 122, 402e (2009)
© The Company of Biologists Limited
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In this issue

SIRT7 gets rDNA transcription going


Figure 1

Over half of the RNA synthesis in the cell takes place during transcription of ribosomal DNA (rDNA) – a nucleolar process that is tightly regulated in response to cell-cycle stage, ageing, starvation and other factors. For instance, rDNA transcription is repressed during mitosis, but we lack a complete picture of how this is controlled. Now, Valentina Sirri and colleagues (p. 489) investigate the mitotic activity of SIRT7, a nucleolar histone deacetylase that has been reported to help regulate rDNA transcription. The authors show that, in contrast to previous reports, SIRT7 associates with nucleolar organiser regions (NORs; the chromosomal sites at which rDNA genes cluster) even when rDNA transcription is repressed, and that this localisation is mediated by a direct interaction between SIRT7 and the rDNA transcription factor UBF. They next show that SIRT7 is phosphorylated by the CDK1–cyclin-B pathway during mitosis, then dephosphorylated before rDNA transcription resumes after mitosis. Moreover, the resumption of transcription requires SIRT7 activity, and the SIRT7 C-terminus becomes more reactive to cognate antibodies before transcription begins. The authors propose, therefore, that dephosphorylation of SIRT7 promotes a change in its conformation, and that this derepresses transcription. Their data underscore the complexity of rDNA transcriptional regulation.


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Related articles in JCS:

Involvement of SIRT7 in resumption of rDNA transcription at the exit from mitosis
Alice Grob, Pascal Roussel, Jane E. Wright, Brian McStay, Danièle Hernandez-Verdun, and Valentina Sirri
JCS 2009 122: 489-498. [Abstract] [Full Text]  




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