4.6 Review

Anaphase B: Long-standing models meet new concepts

Journal

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Volume 117, Issue -, Pages 127-139

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2021.03.023

Keywords

Anaphase B; Spindle elongation; Motor proteins; Microtubule sliding; Chromosome segregation; Microtubule pushing; Microtubule pulling

Funding

  1. European Research Council (ERC) [855158, 647077]
  2. Croatian Science Foundation Cooperation Programme with Croatian Scientists in Diaspora Research Cooper-ability (Croatia) [PZS-2019-02-7653]
  3. European Structural and Investment Funds (ESIF) within the Operational Programme Competitiveness and Cohesion (OPCC) 2014-2020 [KK.01.1.1.04.0057]
  4. Croatian Government, Croatia
  5. European Union through the European Regional Development Fund-the Competitiveness and Cohesion Operational Programme [KK.01.1.1.01.0004]

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This passage discusses the mechanisms of spindle elongation during anaphase B in mitosis, focusing on the core aspects of the process and the roles of anaphase A and B in physically separating sister chromatids.
Mitotic cell divisions ensure stable transmission of genetic information from a mother to daughter cells in a series of generations. To ensure this crucial task is accomplished, the cell forms a bipolar structure called the mitotic spindle that divides sister chromatids to the opposite sides of the dividing mother cell. After successful establishment of stable attachments of microtubules to chromosomes and inspection of connections between them, at the heart of mitosis, the cell starts the process of segregation. This spectacular moment in the life of a cell is termed anaphase, and it involves two distinct processes: depolymerization of microtubules bound to chromosomes, which is also known as anaphase A, and elongation of the spindle or anaphase B. Both processes ensure physical separation of disjointed sister chromatids. In this chapter, we review the mechanisms of anaphase B spindle elongation primarily in mammalian systems, combining different pioneering ideas and concepts with more recent findings that shed new light on the force generation and regulation of biochemical modules operating during spindle elongation. Finally, we present a comprehensive model of spindle elongation that includes structural, biophysical, and molecular aspects of anaphase B.

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