Literature DB >> 34321659

Regulated control of gene therapies by drug-induced splicing.

Alex Mas Monteys1,2, Amiel A Hundley3, Paul T Ranum3, Luis Tecedor3, Amy Muehlmatt3, Euyn Lim3, Dmitriy Lukashev4, Rajeev Sivasankaran4, Beverly L Davidson5,6.   

Abstract

So far, gene therapies have relied on complex constructs that cannot be finely controlled1,2. Here we report a universal switch element that enables precise control of gene replacement or gene editing after exposure to a small molecule. The small-molecule inducers are currently in human use, are orally bioavailable when given to animals or humans and can reach both peripheral tissues and the brain. Moreover, the switch system, which we denote Xon, does not require the co-expression of any regulatory proteins. Using Xon, the translation of the desired elements for controlled gene replacement or gene editing machinery occurs after a single oral dose of the inducer, and the robustness of expression can be controlled by the drug dose, protein stability and redosing. The ability of Xon to provide temporal control of protein expression can be adapted for cell-biology applications and animal studies. Additionally, owing to the oral bioavailability and safety of the drugs used, the Xon switch system provides an unprecedented opportunity to refine and tailor the application of gene therapies in humans.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34321659      PMCID: PMC8966400          DOI: 10.1038/s41586-021-03770-2

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  1 in total

Review 1.  Practical murine hematopathology: a comparative review and implications for research.

Authors:  Karyn E O'Connell; Amy M Mikkola; Aaron M Stepanek; Andyna Vernet; Christopher D Hall; Chia C Sun; Eda Yildirim; John F Staropoli; Jeannie T Lee; Diane E Brown
Journal:  Comp Med       Date:  2015-04       Impact factor: 0.982

  1 in total
  10 in total

Review 1.  Next-generation strategies for gene-targeted therapies of central nervous system disorders: A workshop summary.

Authors:  Jill A Morris; Chris H Boshoff; Nina F Schor; Ling M Wong; Guangping Gao; Beverly L Davidson
Journal:  Mol Ther       Date:  2021-09-20       Impact factor: 11.454

2.  Efficient in vivo base editing via single adeno-associated viruses with size-optimized genomes encoding compact adenine base editors.

Authors:  Jessie R Davis; Xiao Wang; Isaac P Witte; Tony P Huang; Jonathan M Levy; Aditya Raguram; Samagya Banskota; Nabil G Seidah; Kiran Musunuru; David R Liu
Journal:  Nat Biomed Eng       Date:  2022-07-28       Impact factor: 29.234

Review 3.  Therapeutic in vivo delivery of gene editing agents.

Authors:  Aditya Raguram; Samagya Banskota; David R Liu
Journal:  Cell       Date:  2022-07-06       Impact factor: 66.850

Review 4.  Dysregulation and therapeutic targeting of RNA splicing in cancer.

Authors:  Robert F Stanley; Omar Abdel-Wahab
Journal:  Nat Cancer       Date:  2022-05-27

5.  Engineered AAVs for non-invasive gene delivery to rodent and non-human primate nervous systems.

Authors:  Xinhong Chen; Sripriya Ravindra Kumar; Cameron D Adams; Daping Yang; Tongtong Wang; Damien A Wolfe; Cynthia M Arokiaraj; Victoria Ngo; Lillian J Campos; Jessica A Griffiths; Takako Ichiki; Sarkis K Mazmanian; Peregrine B Osborne; Janet R Keast; Cory T Miller; Andrew S Fox; Isaac M Chiu; Viviana Gradinaru
Journal:  Neuron       Date:  2022-05-27       Impact factor: 18.688

Review 6.  Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders.

Authors:  Beverly L Davidson; Guangping Gao; Elizabeth Berry-Kravis; Allison M Bradbury; Carsten Bönnemann; Joseph D Buxbaum; Gavin R Corcoran; Steven J Gray; Heather Gray-Edwards; Robin J Kleiman; Adam J Shaywitz; Dan Wang; Huda Y Zoghbi; Terence R Flotte; Sitra Tauscher-Wisniewski; Cynthia J Tifft; Mustafa Sahin
Journal:  Mol Ther       Date:  2022-05-17       Impact factor: 12.910

7.  An orally available, brain penetrant, small molecule lowers huntingtin levels by enhancing pseudoexon inclusion.

Authors:  Caroline Gubser Keller; Youngah Shin; Alex Mas Monteys; Nicole Renaud; Martin Beibel; Natalia Teider; Thomas Peters; Thomas Faller; Sophie St-Cyr; Judith Knehr; Guglielmo Roma; Alejandro Reyes; Marc Hild; Dmitriy Lukashev; Diethilde Theil; Natalie Dales; Jang-Ho Cha; Beth Borowsky; Ricardo Dolmetsch; Beverly L Davidson; Rajeev Sivasankaran
Journal:  Nat Commun       Date:  2022-03-03       Impact factor: 14.919

Review 8.  Splicing mutations in the CFTR gene as therapeutic targets.

Authors:  Karine Deletang; Magali Taulan-Cadars
Journal:  Gene Ther       Date:  2022-06-02       Impact factor: 4.184

9.  Structural basis of receptor usage by the engineered capsid AAV-PHP.eB.

Authors:  Seongmin Jang; Hao K Shen; Xiaozhe Ding; Timothy F Miles; Viviana Gradinaru
Journal:  Mol Ther Methods Clin Dev       Date:  2022-07-31       Impact factor: 5.849

10.  Cell-specific regulation of gene expression using splicing-dependent frameshifting.

Authors:  Jonathan P Ling; Alexei M Bygrave; Clayton P Santiago; Rogger P Carmen-Orozco; Vickie T Trinh; Minzhong Yu; Yini Li; Ying Liu; Kyra D Bowden; Leighton H Duncan; Jeong Han; Kamil Taneja; Rochinelle Dongmo; Travis A Babola; Patrick Parker; Lizhi Jiang; Patrick J Leavey; Jennifer J Smith; Rachel Vistein; Megan Y Gimmen; Benjamin Dubner; Eric Helmenstine; Patric Teodorescu; Theodoros Karantanos; Gabriel Ghiaur; Patrick O Kanold; Dwight Bergles; Ben Langmead; Shuying Sun; Kristina J Nielsen; Neal Peachey; Mandeep S Singh; W Brian Dalton; Fatemeh Rajaii; Richard L Huganir; Seth Blackshaw
Journal:  Nat Commun       Date:  2022-10-01       Impact factor: 17.694

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.