Literature DB >> 36040590

Generation of Atrial-Specific Construct Using Sarcolipin Promoter-Associated CRM4 Enhancer.

Dongtak Jeong1.   

Abstract

Cardiac gene therapy has been hampered by off-target expression of gene of interest irrespective of variety of delivery methods. To overcome this issue, cardiac-specific promoters provide target tissue specificity, although expression is often debilitated compared to that of ubiquitous promoters. We have previously shown that sarcolipin promoter with an enhancer calsequestrin cis-regulatory module 4 (CRM4) combination has an improved atrial specificity. Moreover, it showed a minimal extra-atrial expression, which is a significant advantage for AAV9-mediated cardiac gene therapy. Therefore, it can be a useful tool to study and treat atrial-specific diseases such as atrial fibrillation. In this chapter, we introduce practical and simple methodology for atrial-specific gene therapy using sarcolipin promoter with an enhancer CRM4.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  AAV9; Atrium; CRM4; Cis-acting regulatory module; Gene therapy; Sarcolipin

Mesh:

Substances:

Year:  2022        PMID: 36040590     DOI: 10.1007/978-1-0716-2707-5_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Subtype-specific promoter-driven action potential imaging for precise disease modelling and drug testing in hiPSC-derived cardiomyocytes.

Authors:  Zhifen Chen; Wenying Xian; Milena Bellin; Tatjana Dorn; Qinghai Tian; Alexander Goedel; Lisa Dreizehnter; Christine M Schneider; Dorien Ward-van Oostwaard; Judy King Man Ng; Rabea Hinkel; Luna Simona Pane; Christine L Mummery; Peter Lipp; Alessandra Moretti; Karl-Ludwig Laugwitz; Daniel Sinnecker
Journal:  Eur Heart J       Date:  2017-01-21       Impact factor: 29.983

  1 in total

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