Nicotine exposure caused significant transgenerational heritable behavioral changes in Caenorhabditis elegans
نویسندگان
چکیده
Passive and active exposure to tobacco smoking among youth is directly associated with immediate as well as long-term health deterioration. Despite all public health policies and efforts, the percentage of teenage smokers is still relatively high, especially in developing countries. Very few, if any, studies have been done on the transgenerational effect of nicotine exposed during the more sensitive, early developmental stages. We employed C. elegans as a biological model to study the multigenerational impact of chronic nicotine exposure. Nicotine treatment was limited to N2 hermaphrodites of the F0 generation. Exposure was limited to the larval period L1-L4 (~31 hours) after which worms were transferred to a fresh NGM plate. N2 hermaphrodites at L4 developmental stage were used for behavioral analysis across three generations: F0, F1, and F2. Our results show that nicotine was associated with changes in sinusoidal locomotion, speed, and body bends in L4 larvae in all three tested generations. These behavioral alterations were not restricted to F0, but were observed in F1 and F2 generations which were never exposed to nicotine. Our study is the first to reveal that nicotine addiction is heritable using C. elegans as a model organism. These results underscored the sensitivity of early development stages, with hope to spread more awareness to encourage the avoidance of nicotine exposure, especially at a young age.
منابع مشابه
Establishment and Maintenance of Heritable Chromatin in C. elegans
Mounting evidence suggests that environmental exposures in one generation may result in changes in gene expression that are heritable for multiple generations, yet are unaccompanied by genetic mutations. These phenomena are considered to be the result of epigenetic mechanisms, which can establish metastable states of chromatin-based genome architecture that can be passed through the gametes int...
متن کاملTransgenerational Diapause as an Avoidance Strategy against Bacterial Pathogens in Caenorhabditis elegans
The dynamic response of organisms exposed to environmental pathogens determines their survival or demise, and the outcome of this interaction depends on the host's susceptibility and pathogen-dependent virulence factors. The transmission of acquired information about the nature of a pathogen to progeny may ensure effective defensive strategies for the progeny's survival in adverse environments....
متن کاملA Tunable Mechanism Determines the Duration of the Transgenerational Small RNA Inheritance in C. elegans
In C. elegans, small RNAs enable transmission of epigenetic responses across multiple generations. While RNAi inheritance mechanisms that enable "memorization" of ancestral responses are being elucidated, the mechanisms that determine the duration of inherited silencing and the ability to forget the inherited epigenetic effects are not known. We now show that exposure to dsRNA activates a feedb...
متن کاملHeritable Transmission of Stress Resistance by High Dietary Glucose in Caenorhabditis elegans
Glucose is a major energy source and is a key regulator of metabolism but excessive dietary glucose is linked to several disorders including type 2 diabetes, obesity and cardiac dysfunction. Dietary intake greatly influences organismal survival but whether the effects of nutritional status are transmitted to the offspring is an unresolved question. Here we show that exposing Caenorhabditis eleg...
متن کاملTargeted heritable mutation and gene conversion by Cas9-CRISPR in Caenorhabditis elegans.
We have achieved targeted heritable genome modification in Caenorhabditis elegans by injecting mRNA of the nuclease Cas9 and Cas9 guide RNAs. This system rapidly creates precise genomic changes, including knockouts and transgene-instructed gene conversion.
متن کامل