Impoverished Conceptions of Gene Causation and Therapy in Developmental Neurology.

Antisense Gene therapy Genetic disease Phenotype

Journal

Pediatric neurology
ISSN: 1873-5150
Titre abrégé: Pediatr Neurol
Pays: United States
ID NLM: 8508183

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 12 03 2023
revised: 09 06 2023
accepted: 23 07 2023
pubmed: 1 9 2023
medline: 1 9 2023
entrez: 31 8 2023
Statut: ppublish

Résumé

We offer a primer to the modifiability of genetic neurological disease, particularly during development. One goal is to harness several unexpected observations made in the course of experimental gene modification or therapy into an explanatory conceptual context based on biological first principles. To this end, we anchor growing, disparate reports of unusual or untoward effects to a plausible framework wherein genes exhibit different degrees of modifiability and may result, when mutated or therapeutically modified, in unsuspected consequences. We propose that genetic pathogenic variant effects and modifiability depend on the number and complexity of associated protein-protein or higher-order interactions. Thus, gene malleability may range from that characteristic of the favorably modifiable primarily structural genes that subserve relatively invariant or circumscribed phenomena such as cell shape to that typical of some transcription factors, which are less functionally predictable when altered. The latter may be expressed developmentally, in compartmentalized manner, or only intermittently and yet exert vastly ramified influences sometimes circumscribed only to select species. We also argue that genetic diseases may steer the organism toward often poorly understood biological end points and co-opt multiple processes into hardly modifiable biology. Addition or modification of genes to approximate a normal state not previously experienced by the organism may lead to further aberration due to extraneous interference with the native biology of the disease state. Therefore, an understanding as perspicuous as possible of gene function, regulation, modifiability, and biological directionality down to seemingly minute but disease-relevant consequences is a prerequisite to intervention. Although we provide some groundwork steps to such an understanding, this may occasionally prove unattainable.

Identifiants

pubmed: 37652816
pii: S0887-8994(23)00225-4
doi: 10.1016/j.pediatrneurol.2023.07.017
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

198-205

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS077015
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS094257
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS102588
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Juan M Pascual (JM)

Rare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas; Department of Physiology, The University of Texas Southwestern Medical Center, Dallas, Texas; Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, Texas; Eugene McDermott Center for Human Growth & Development/Center for Human Genetics, The University of Texas Southwestern Medical Center, Dallas, Texas. Electronic address: Juan.Pascual@UTSouthwestern.edu.

Vikram Jakkamsetti (V)

Rare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas.

Ignacio Málaga (I)

Rare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas.

Denis Noble (D)

Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.

Classifications MeSH