The anaphase-promoting complex: it's not just for mitosis any more

  1. J. Wade Harper1,3,
  2. Janet L. Burton2, and
  3. Mark J. Solomon2
  1. 1Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030, USA; 2Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8024, USA

This extract was created in the absence of an abstract.

The ability of cells to make exact replicas of themselves is central to the life and development of complex organisms. Initial insights into the question of how cells divide came during the latter half of the 19th century when Walther Flemming visualized structures he called threads (which we now call chromosomes) and described how these threads change during cell multiplication, a process he called mitosis. Now, more than a century later, we have a molecular understanding of many of the cellular processes that Flemming observed. Indeed, major cytological events occurring during mitosis are known to constitute cell cycle transitions and are regulated by complex signal transduction pathways whose major components have been identified during the past decade. In this review, we describe recent efforts to understand how central components of this regulatory apparatus—cyclin-dependent kinases and the anaphase-promoting complex/cyclosome (APC/C)—control progression through the cell division cycle and how regulatory mechanisms impinge on the APC/C. The APC/C is the multisubunit ubiquitin ligase whose activity is precisely regulated to ensure the timely degradation of cyclins and other key cell cycle regulators in unperturbed cells and to respond to mitotic checkpoints that prevent their degradation. We pay particular attention to recent developments as excellent reviews are available from a few years ago (Morgan 1999; Zachariae and Nasmyth 1999).

Cell cycle transitions: interplay between cyclin-dependent kinases and ubiquitin-mediated proteolysis

The primary task of the cell division cycle is to duplicate genetic information precisely through the process of DNA replication (S phase) and then to allocate this information equally to two daughter cells through mitosis. Inaccuracies in this process can be problematic. For example, cells that attempt to separate chromosomes that are incorrectly or incompletely duplicated are much more likely to incur fatal or irreparable damage as a result of either loss or gain of genetic information. Thus, a large number of signaling pathways …

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