Human skin cells (both normal and xeroderma pigmentosum) were treated with carbaryl (N-methyl-1-naphthyl-carbamate), a common agricultural pesticide, or its N-nitroso derivative, nitrosocarbaryl, and the DNA of the cells was sedimented in alkaline sucrose gradients at several times after treatment. Numerous single-strand breaks were apparent in the DNA of the nitrosocarbaryl-treated cells but not in the DNA of those treated with carbaryl. The nitrosocarbaryl effect on the DNA could be observed up to 20 h after removal of the chemical from the cultures. The DNA of human cells treated with ring labeled nitroso[3H]carbaryl and methyl labeled nitroso[14C]carbaryl was isolated and banded in cesium chloride density gradients. The peak of 14C radioactivity and not the 3H radioactivity coincided with the optical density peak of the human DNA from these gradients. An aliquot of the same DNA was alkaline denatured and banded on alkaline cesium chloride gradients with similar results. These observations suggest that the nitrosocarbaryl molecule is split and only the methyl containing residue forms an irreversible association with human cellular DNA, resulting in chemical changes observable as alkali-sensitive bonds.

Download full-text PDF

Source
http://dx.doi.org/10.1016/0165-1161(76)90153-9DOI Listing

Publication Analysis

Top Keywords

dna
9
human dna
8
dna human
8
treated carbaryl
8
nitrosocarbaryl dna
8
cesium chloride
8
nitrosocarbaryl
4
nitrosocarbaryl human
4
human
4
human skin
4

Similar Publications

: Major Depressive Disorder (MDD) is a prevalent and debilitating mental disorder that has been linked to hyperhomocysteinemia and folate deficiency. These conditions are influenced by the methylenetetrahydrofolate reductase () gene, which plays a crucial role in converting homocysteine to methionine and is essential for folate metabolism and neurotransmitter synthesis, including serotonin. : This study explored the association between and polymorphisms among Saudi MDD patients attending the Erada Complex for Mental Health and Erada Services outpatient clinic in Jeddah, Saudi Arabia.

View Article and Find Full Text PDF

Decoding the Molecular Enigma Behind Asbestos and Fibrous Nanomaterial-induced carcinogenesis.

J Occup Health

January 2025

Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

Objectives: Natural fibrous mineral, asbestos, has been useful in industry for many centuries. In the 1960's, epidemiology had recognized the association between asbestos exposure and mesothelioma and the IARC designated all kinds of asbestos as Group 1 in 1987. However, various scientific enigmas remained regarding the molecular mechanisms of asbestos-induced mesothelial carcinogenesis.

View Article and Find Full Text PDF

Histone Modifications and DNA Methylation in Psoriasis: A Cellular Perspective.

Clin Rev Allergy Immunol

January 2025

Department of Dermatology and Venereology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

In recent years, epigenetic modifications have attracted significant attention due to their unique regulatory mechanisms and profound biological implications. Acting as a bridge between environmental stimuli and changes in gene activity, they reshape gene expression patterns, providing organisms with regulatory mechanisms to respond to environmental changes. A growing body of evidence indicates that epigenetic regulation plays a crucial role in the pathogenesis and progression of psoriasis.

View Article and Find Full Text PDF

Perfluorooctane sulfonic acid (PFOS) is an anthropogenic chemical found in aqueous film-forming foams (AFFFs) and many consumer products. Despite its environmental ubiquity and persistence, little is known about the effects of PFOS on stress levels in wild animals. Here, we examined PFOS bioaccumulation and correlations between PFOS exposure and oxidative stress in snapping turtles (Chelydra serpentina) downstream of Griffiss Air Force Base in Rome, New York, a known source of AFFF contamination.

View Article and Find Full Text PDF

Homologous recombination is a largely error-free DNA repair mechanism conserved across all domains of life and is essential for the maintenance of genome integrity. Not only are the mutations in homologous recombination repair genes probable cancer drivers, some also cause genetic disorders. In particular, mutations in the Bloom (BLM) helicase cause Bloom Syndrome, a rare autosomal recessive disorder characterized by increased sister chromatid exchanges and predisposition to a variety of cancers.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!