Transmission dynamics of heritable silencing induced by double-stranded RNA in Caenorhabditis elegans

Heritable silencing effects are gene suppression phenomena that can persist for generations after induction. In the majority of RNAi experiments conducted in Caenorhabditis elegans, the silencing response results in a hypomorphic phenotype where the effects recede after the F1 generation. F2 and subsequent generations revert to the original phenotype. Specific examples of transgenerational RNAi in which effects persist to the F2 generation and beyond have been described. In this study, we describe a systematic pedigree-based analysis of heritable silencing processes resulting from initiation of interference targeted at the C. elegans oocyte maturation factor oma-1. Heritable silencing of oma-1 is a dose-dependent process where the inheritance of the silencing factor is unequally distributed among the population. Heritability is not constant over generational time, with silenced populations appearing to undergo a bottleneck three to four generations following microinjection of RNA. Transmission of silencing through these generations can be through either maternal or paternal gamete lines and is surprisingly more effective through the male gametic line. Genetic linkage tests reveal that silencing in the early generations is transmitted independently of the original targeted locus, in a manner indicative of a diffusible epigenetic element.

Medienart:

E-Artikel

Erscheinungsjahr:

2008

Erschienen:

2008

Enthalten in:

Zur Gesamtaufnahme - volume:180

Enthalten in:

Genetics - 180(2008), 3 vom: 30. Nov., Seite 1275-88

Sprache:

Englisch

Beteiligte Personen:

Alcazar, Rosa M [VerfasserIn]
Lin, Rueyling [VerfasserIn]
Fire, Andrew Z [VerfasserIn]

Links:

Volltext

Themen:

Caenorhabditis elegans Proteins
Carrier Proteins
Journal Article
OMA-1 protein, C elegans
RNA, Double-Stranded
RNA, Small Interfering
Research Support, N.I.H., Extramural

Anmerkungen:

Date Completed 06.02.2009

Date Revised 20.10.2021

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1534/genetics.108.089433

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM182108473