학술논문

A DNA repair pathway can regulate transcriptional noise to promote cell fate transitions
Document Type
article
Source
Science. 373(6557)
Subject
Genetics
1.1 Normal biological development and functioning
Underpinning research
Generic health relevance
Animals
Cell Differentiation
Cells
Cultured
Cellular Reprogramming
Computer Simulation
DNA
DNA Repair
DNA-(Apurinic or Apyrimidinic Site) Lyase
Embryonic Stem Cells
Gene Expression
Idoxuridine
Mice
Models
Genetic
Nanog Homeobox Protein
Nucleic Acid Conformation
RNA
Messenger
Single-Cell Analysis
Stochastic Processes
Thymidine Kinase
Transcription
Genetic
General Science & Technology
Language
Abstract
Stochastic fluctuations in gene expression ("noise") are often considered detrimental, but fluctuations can also be exploited for benefit (e.g., dither). We show here that DNA base excision repair amplifies transcriptional noise to facilitate cellular reprogramming. Specifically, the DNA repair protein Apex1, which recognizes both naturally occurring and unnatural base modifications, amplifies expression noise while homeostatically maintaining mean expression levels. This amplified expression noise originates from shorter-duration, higher-intensity transcriptional bursts generated by Apex1-mediated DNA supercoiling. The remodeling of DNA topology first impedes and then accelerates transcription to maintain mean levels. This mechanism, which we refer to as "discordant transcription through repair" ("DiThR," which is pronounced "dither"), potentiates cellular reprogramming and differentiation. Our study reveals a potential functional role for transcriptional fluctuations mediated by DNA base modifications in embryonic development and disease.