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用于研究芽殖酵母中II型拓扑异构酶的酵母工具。

Yeast Tools for Studying Type II Topoisomerases in Budding Yeast.

作者信息

McCoy Maureen Nie, Adhikari Myna, Nitiss Karin C, Nitiss John L

机构信息

Pharmaceutical Sciences Department, Retzky College of Pharmacy, University of Illinois Chicago, Rockford, IL, USA.

Biomedical Sciences Department, University of Illinois College of Medicine, Rockford, IL, USA.

出版信息

Methods Mol Biol. 2025;2928:123-150. doi: 10.1007/978-1-0716-4550-5_12.


DOI:10.1007/978-1-0716-4550-5_12
PMID:40372643
Abstract

DNA topoisomerases perform diverse functions in DNA metabolism. Type II topoisomerases, which carry out their reaction through a double-strand break intermediate, are absolutely required to separate replicated chromosomes prior to mitosis and play key roles in replication, transcription, and chromosome stability. The yeast Saccharomyces cerevisiae has been a premier system for exploring the biological roles of topoisomerases, and since type II enzymes are required for viability, the availability of conditional mutants greatly enhances the ability to dissect their biological roles. This chapter provides a critical discussion of yeast top2 mutants and plasmids for expressing and genetically manipulating the gene encoding the enzyme. An additional advantage of the yeast is the ability to functionally express human Top2α and Top2β in yeast to determine whether the human enzymes have unique characteristics that impact their biological functions. Therefore, this chapter also discusses plasmids that are available to express human Top2 enzymes in yeast. Finally, yeast has been particularly valuable in studying anti-cancer drugs that target Top2. This chapter discusses novel and powerful approaches for enhancing drug accumulation, allowing detailed examination of various topoisomerase inhibitors and poisons.

摘要

DNA拓扑异构酶在DNA代谢中发挥着多种功能。II型拓扑异构酶通过双链断裂中间体进行反应,在有丝分裂前分离复制后的染色体是绝对必需的,并且在复制、转录和染色体稳定性中发挥关键作用。酿酒酵母一直是探索拓扑异构酶生物学作用的首要系统,由于II型酶对于细胞存活是必需的,条件性突变体的可用性极大地增强了剖析其生物学作用的能力。本章对酵母top2突变体以及用于表达和基因操作该酶编码基因的质粒进行了批判性讨论。酵母的另一个优势是能够在酵母中功能性表达人Top2α和Top2β,以确定人源酶是否具有影响其生物学功能的独特特征。因此,本章还讨论了可用于在酵母中表达人Top2酶的质粒。最后,酵母在研究靶向Top2的抗癌药物方面特别有价值。本章讨论了增强药物积累的新颖而强大的方法,从而能够详细研究各种拓扑异构酶抑制剂和毒物。

相似文献

[1]
Yeast Tools for Studying Type II Topoisomerases in Budding Yeast.

Methods Mol Biol. 2025

[2]
Analysis of yeast DNA topoisomerase II mutants resistant to the antitumor drug amsacrine.

Cancer Res. 1994-4-1

[3]
Regulation of topoisomerase II stability and activity by ubiquitination and SUMOylation: clinical implications for cancer chemotherapy.

Mol Biol Rep. 2021-9

[4]
The nucleotide sequence of the fission yeast DNA topoisomerase II gene: structural and functional relationships to other DNA topoisomerases.

EMBO J. 1986-9

[5]
Monitoring the DNA Topoisomerase II Checkpoint in Saccharomyces cerevisiae.

Methods Mol Biol. 2018

[6]
Topoisomerase IIα, rather than IIβ, is a promising target in development of anti-cancer drugs.

Drug Discov Ther. 2012-10

[7]
Molecular cloning and expression of the Candida albicans TOP2 gene allows study of fungal DNA topoisomerase II inhibitors in yeast.

Biochem J. 1997-5-15

[8]
Identification of yeast DNA topoisomerase II mutants resistant to the antitumor drug doxorubicin: implications for the mechanisms of doxorubicin action and cytotoxicity.

Mol Pharmacol. 1997-10

[9]
Human DNA topoisomerases II alpha and II beta can functionally substitute for yeast TOP2 in chromosome segregation and recombination.

Mol Gen Genet. 1996-8-27

[10]
SUMO-Targeted DNA Translocase Rrp2 Protects the Genome from Top2-Induced DNA Damage.

Mol Cell. 2017-5-25

本文引用的文献

[1]
Use of CRISPR/Cas9 with Homology-Directed Repair to Gene-Edit Topoisomerase II in Human Leukemia K562 Cells: Generation of a Resistance Phenotype.

J Pharmacol Exp Ther. 2024-4-18

[2]
Deletions initiated by the vaccinia virus TopIB protein in yeast.

DNA Repair (Amst). 2024-5

[3]
Single-molecule visualization of twin-supercoiled domains generated during transcription.

Nucleic Acids Res. 2024-2-28

[4]
Bacteria and Yeast Colony PCR.

Methods Mol Biol. 2023

[5]
Naturally mutagenic sequence diversity in a human type II topoisomerase.

Proc Natl Acad Sci U S A. 2023-7-11

[6]
Auxin-inducible degron system: an efficient protein degradation tool to study protein function.

Biotechniques. 2023-4

[7]
Basis for the discrimination of supercoil handedness during DNA cleavage by human and bacterial type II topoisomerases.

Nucleic Acids Res. 2023-5-8

[8]
High-efficiency recombinant protein purification using mCherry and YFP nanobody affinity matrices.

Protein Sci. 2022-9

[9]
Topoisomerase I inhibitors: Challenges, progress and the road ahead.

Eur J Med Chem. 2022-6-5

[10]
Sister chromatids separate during anaphase in a three-stage program as directed by interaxis bridges.

Proc Natl Acad Sci U S A. 2022-3-8

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