Literature DB >> 29523238

Methods for Controlled Protein Depletion to Study Protein Function during Meiosis.

Hardeep Kaur1, Jasvinder S Ahuja1, Michael Lichten2.   

Abstract

Proteins with potential roles in meiotic recombination often have essential or important functions during the mitotic cell cycle. In addition, proteins may have different functions at different times during meiosis. In such cases, it can be challenging to precisely determine protein function during meiosis using null or hypomorphic mutants. One example is the Sgs1-Top3-Rmi1 helicase-decatenase complex, which is required for normal vegetative growth and genome stability. In such cases, conditional loss-of-function mutants can be useful. In this chapter, we describe the construction of two types of conditional mutants, meiotic depletion alleles and auxin-induced degradation alleles, that allow protein depletion specifically during budding yeast meiosis, and illustrate their use with Sgs1. We also describe a modified method for the isolation of meiotic recombination intermediates that combines previous psoralen cross-linking and cetyltrimethylammonium bromide isolation methods.
© 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Auxin-induced degron; Budding yeast; CTAB–psoralen cross-linking DNA preparation; Meiosis; Meiotic depletion; Nuclear divisions; Protein levels; Recombination intermediate; Saccharomyces; Sgs1–topoisomerase III–Rmi1 complex

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Year:  2018        PMID: 29523238     DOI: 10.1016/bs.mie.2017.11.032

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  7 in total

1.  Turning coldspots into hotspots: targeted recruitment of axis protein Hop1 stimulates meiotic recombination in Saccharomyces cerevisiae.

Authors:  Anura Shodhan; Martin Xaver; David Wheeler; Michael Lichten
Journal:  Genetics       Date:  2022-08-30       Impact factor: 4.402

2.  Repeated strand invasion and extensive branch migration are hallmarks of meiotic recombination.

Authors:  Jasvinder S Ahuja; Catherine S Harvey; David L Wheeler; Michael Lichten
Journal:  Mol Cell       Date:  2021-08-27       Impact factor: 19.328

3.  Noncanonical Contributions of MutLγ to VDE-Initiated Crossovers During Saccharomyces cerevisiae Meiosis.

Authors:  Anura Shodhan; Darpan Medhi; Michael Lichten
Journal:  G3 (Bethesda)       Date:  2019-05-07       Impact factor: 3.154

4.  S. cerevisiae Srs2 helicase ensures normal recombination intermediate metabolism during meiosis and prevents accumulation of Rad51 aggregates.

Authors:  Laura J Hunt; Emad A Ahmed; Hardeep Kaur; Jasvinder S Ahuja; Lydia Hulme; Ta-Chung Chou; Michael Lichten; Alastair S H Goldman
Journal:  Chromosoma       Date:  2019-05-09       Impact factor: 4.316

5.  Unresolved Recombination Intermediates Cause a RAD9-Dependent Cell Cycle Arrest in Saccharomyces cerevisiae.

Authors:  Hardeep Kaur; Krishnaprasad Gn; Michael Lichten
Journal:  Genetics       Date:  2019-09-27       Impact factor: 4.562

6.  Interplay between Pds5 and Rec8 in regulating chromosome axis length and crossover frequency.

Authors:  Meihui Song; Binyuan Zhai; Xiao Yang; Taicong Tan; Ying Wang; Xuan Yang; Yingjin Tan; Tingting Chu; Yanding Cao; Yulong Song; Shunxin Wang; Liangran Zhang
Journal:  Sci Adv       Date:  2021-03-12       Impact factor: 14.136

7.  C-Terminal HA Tags Compromise Function and Exacerbate Phenotypes of Saccharomyces cerevisiae Bloom's Helicase Homolog Sgs1 SUMOylation-Associated Mutants.

Authors:  Matan Cohen; Michael Lichten
Journal:  G3 (Bethesda)       Date:  2020-08-05       Impact factor: 3.154

  7 in total

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