| Literature DB >> 32473090 |
Richik Nilay Mukherjee1, Jérémy Sallé2, Serge Dmitrieff2, Katherine M Nelson3, John Oakey3, Nicolas Minc4, Daniel L Levy5.
Abstract
Nuclear size plays pivotal roles in gene expression, embryo development, and disease. A central hypothesis in organisms ranging from yeast to vertebrates is that nuclear size scales to cell size. This implies that nuclei may reach steady-state sizes set by limiting cytoplasmic pools of size-regulating components. By monitoring nuclear dynamics in early sea urchin embryos, we found that nuclei undergo substantial growth in each interphase, reaching a maximal size prior to mitosis that declined steadily over the course of development. Manipulations of cytoplasmic volume through multiple chemical and physical means ruled out cell size as a major determinant of nuclear size and growth. Rather, our data suggest that the perinuclear endoplasmic reticulum, accumulated through dynein activity, serves as a limiting membrane pool that sets nuclear surface growth rate. Partitioning of this local pool at each cell division modulates nuclear growth kinetics and dictates size scaling throughout early development.Entities:
Keywords: cell size; embryonic development; nuclear size scaling; nuclear-to-cytoplasmic ratio; nucleus; paracentrotus lividus sea urchins; perinuclear endoplasmic reticulum; xenopus laevis frogs
Year: 2020 PMID: 32473090 PMCID: PMC7423768 DOI: 10.1016/j.devcel.2020.05.003
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270