TIGRa: An ultra-compact programmable activator enabling multiplexed and efficient gene regulation

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Authors: Zhiquan Liu, Siyu Chen, Wenmin Wang, Fan Zhang, Qing Wang, Grzegorz Walkiewicz, Faruk Hossen, Jinqiong Zhou, Yiting Wang, Yang Sun
Cited by: 1
References: 51

Abstract

Programmable gene activation has broad therapeutic potential but remains constrained by the large effector size, limited multiplexing capacity, and challenges in in vivo delivery. Here, we develop the TIGR-TasR-mediated activator (TIGRa), a compact transcriptional activator derived from the tandem interspaced guide RNA (TIGR)-TIGR-associated protein (TasR) system that is mechanistically distinct from CRISPR-based activators. TIGRa is less than half the size of dSpCas9-based activators while achieving comparable or greater activation efficiency. Its native TIGR array architecture enables efficient multiplexed regulation, supporting simultaneous activation of up to 12 endogenous genes from a single compact construct. TIGRa-mediated multi-gene activation efficiently reprogrammed human fibroblasts into induced pluripotent stem cells. In addition, an all-in-one adeno-associated virus (AAV)-TIGRa vector activated endogenous CaMKII in vivo, promoting retinal ganglion cell survival and preserving visual function in a mouse model of N-methyl-D-aspartic (NMDA)-induced retinal injury. These results establish TIGRa as a compact and multiplexable platform for therapeutic gene regulation and in vivo genetic medicine.

Fields of Study & Subjects

CRISPR and Genetic Engineering Retinal Development and Disorders RNA regulation and disease

Publication details

Journal / source
Cell stem cell
Publisher
Elsevier BV
Volume
33
Issue
9
Pages
1553–1566.e4
Publication date
10 August 2026
Language
EN