Protocol

Isolation and Demembranation of Xenopus Sperm Nuclei

  1. Jesse C. Gatlin1,3
  1. 1Department of Molecular Biology, University of Wyoming, Laramie, Wyoming 82071
  1. 3Correspondence: jgatlin{at}uwyo.edu
  • 2 Present address: Center for Biomedical Ethics and Society, Institute for Medicine and Public Health, Vanderbilt University Medical Center, Nashville, Tennessee 37203

Abstract

The inherent experimental advantages of intact amphibian eggs have been exploited for several decades to advance our understanding of fundamental developmental processes and the cell cycle. Characterization of these processes at the molecular level has been greatly advanced by the use of cell-free extracts, which permit the development of biochemically tractable approaches. Demembranated Xenopus laevis sperm nuclei have been used with cell-free extracts to recapitulate cell cycle progression and to control the cell cycle state of the egg extract. This system has become an invaluable and widely used tool for studies of cell cycle regulation and many downstream events. Here, we describe a protocol, derived in part from other published protocols and modified over time, for the preparation of Xenopus sperm nuclei that can be used in a variety of in vitro assays.

Footnotes

  • From the Xenopus collection, edited by Hazel L. Sive.

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  1. Cold Spring Harb Protoc © 2018 Cold Spring Harbor Laboratory Press
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