1. Poly(ADP-ribose) synthesized in nuclei isolated from Friend erythroleukemic cells was characterized. Although the activity of poly(ADP-ribose) synthesis of cells induced to differentiate was suppressed to about one-third of that of uninduced cells, the chain length were identical, and were clearly restricted within a narrow band in polyacrylamide gels, moving at about half the speed of bromphenol blue. 2. The restriction of chain length was also observed in rat liver nuclei, though some poly(ADP-ribose) chains could be degraded into smaller pieces during incubation. Treatment of nuclei with a high concentration of detergent and sonication before incubation caused aberrant synthesis of poly(ADP-ribose) chains which were not restricted in size. 3. In contrast, the average chain length of the 3H-labeled portion of poly(ADP-ribose) synthesized during incubation of nuclei with 3H-NAD+ was found to be reduced to 50% of that in the induced cells. 4. Under our reaction conditions, about 95% of newly synthesized poly(ADP-ribose) was linked to non-histone nuclear proteins. The total content of the non-histones was reduced to about 50% by treatment with inducers. 5. In view of the above findings, it is suggested that the decrease of chain initiation frequency caused by the partial loss of available acceptor sites may be correlated with the suppression of poly(ADP-ribose) synthesis in induced cells.
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http://dx.doi.org/10.1093/oxfordjournals.jbchem.a132998 | DOI Listing |
Bioengineered
December 2025
Department of Biotechnology, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.
Polyhydroxyalkanoates (PHA) are bioplastics produced by few bacteria as intracellular lipid inclusions under excess carbon source and nutrient-deprived conditions. These polymers are biodegradable and resemble petroleum-based plastics. The rising environmental concerns have increased the demand for PHA, but the low yield in wild-type bacterial strains limits large-scale production.
View Article and Find Full Text PDFBMJ Nutr Prev Health
December 2024
Department of Nutrition and Food Technology, The University of Jordan, Amman, Jordan.
Background: Postprandial lipemia (PPL) has been recognised as a cardiovascular disease risk factor. Appetite and PPL can be influenced by the length of saturated fatty acids (FAs). Thus, this study aims to investigate if different FA chain lengths have different impacts on appetite and PPL in healthy volunteers.
View Article and Find Full Text PDFDiabetes Metab Syndr Obes
January 2025
Department of Clinical Laboratory, Guangxi Academy of Medical Sciences, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, 530021, People's Republic of China.
Objective: To investigate the allelic genotypes of the adiponectin (APN) gene polymorphisms (rs1501299) and its association with APN level among Mets patients.
Methods: A total of 410 patients with Mets and 203 healthy subjects were included in the study. The serum APN levels of the subjects were detected using enzyme-linked immunosorbent assay.
J Pharm Anal
December 2024
MTA-HUN-REN TTK Lendület "Momentum" Peptide-Based Vaccines Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Budapest, H-1117, Hungary.
The aim of the research is to increase the applicability of lipopeptides as drugs. To this end, non-ionic triblock copolymers, namely poloxamers, were applied. The physico-chemical properties of poloxamers vary depending on the length of the blocks.
View Article and Find Full Text PDFSovrem Tekhnologii Med
January 2025
MD, DSc, Professor, Chief Researcher, Laboratory of Molecular Genetic Testing of Therapeutic Diseases; Institution of Internal and Preventive Medicine - Branch of the Federal Research Center Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 175/1 B. Bogatkova St., Novosibirsk, 630089, Russia.
Unlabelled: was to search for the associations of benign unconjugated hyperbilirubinemia phenotype with rs1799945 (H63D), rs1800562 (C282Y), rs1800730 (S65C) mutations of gene, rs113993960 (ΔF508) of gene, rs28929474 (PIZ), rs17580 (PIS) mutations of gene.
Material And Methods: The study design is case-control. The group with Gilbert's syndrome (GS) phenotype (n=414; mean age - 36.
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