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用于组织特异性生长素诱导降解以及用于表征Cre和Flp驱动因子的新型基于Flexon的试剂

New Flexon-based reagents for tissue-specific Auxin-Inducible Degradation and for characterizing Cre and Flp drivers in .

作者信息

Wittes Julia, Greenwald Iva

机构信息

Dept. of Biological Sciences, Columbia University, New York, New York, USA.

出版信息

MicroPubl Biol. 2024 Aug 19;2024. doi: 10.17912/micropub.biology.001315. eCollection 2024.

Abstract

A Flexon stop cassette interrupts translation of a coding region until it is excised by a recombinase to allow for gene expression. We have expanded options for Auxin-Inducible Degradation by generating Flexon-based transgenes for tissue-specific expression of the ubiquitin ligase substrate recognition component TIR1 or the variant TIR1(F79G) after excision of the Flexon by Cre recombinase. We also describe Flexon-based tester transgenes to facilitate gathering accurate information about the expression pattern of Cre and Flp recombinase drivers that can be used in conjunction with any conditional expression reagents that utilize these recombinases.

摘要

Flexon终止盒会中断编码区的翻译,直到它被重组酶切除以允许基因表达。我们通过生成基于Flexon的转基因来扩展生长素诱导降解的选择,这些转基因用于在Flexon被Cre重组酶切除后组织特异性表达泛素连接酶底物识别组件TIR1或变体TIR1(F79G)。我们还描述了基于Flexon的测试转基因,以促进收集有关Cre和Flp重组酶驱动子表达模式的准确信息,这些驱动子可与利用这些重组酶的任何条件性表达试剂一起使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/11369693/f1e7259c1146/25789430-2024-micropub.biology.001315.jpg

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