## Abstract A butyric acid pro‐drug, pivaloyioxymethyl butyrate, AN‐9, developed in our laboratory, was previously shown to act as a differentiation‐inducing and an anti‐cancer agent. In this study we have shown that both AN‐9 and butyric acid caused a transient hyperacetylation of histones, which
The program of Hl histone synthesis inS. purpuratus embryos and the control of its timing
✍ Scribed by Harrison, M. Frances ;Wilt, Fred H.
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 977 KB
- Volume
- 223
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The program of H1 histone synthesis was investigated in Strongylocentrotus purpuratus embryos in order to determine when the late Hl histones are synthesized. The embryos were staged by cell number, morphological stage, and chronological age. Care was taken to ensure that conditions of rearing the embryos remained consistent. Labelling with 3H‐lysine revealed that two forms of early Hl (Hlα~1~, and Hlα~2~) are synthesized from early cleavage stages (16–32 cells) to the blastula stage. Hlα~1~, synthesis ceases first at around 400 cells (hatching blastula); Hlα~2~ continues to be synthesized by the blastula but is usually absent from the labelling pattern in early gastrula (700 cells). Two forms of late Hl γ appear sequentially during the pre‐hatching blastula stage. Hl γ appears at 200–250 cells and Hl β approximately 1 hr later, at 250–300 cells. The late forms of H2A and H2B are first synthesized at around hatching, several hours after late Hl forms appear. The time of synthesis of late Hl is strictly controlled by a chronological clock and is not affected by disruption of the cell cycle, cessation of DNA synthesis, or alteration of nucleocytoplasmic ratios. Polyspermic embryos and hydroxyurea‐arrested embryos followed the normal temporal program of on‐ set of late Hl synthesis.
📜 SIMILAR VOLUMES
## Abstract Using collagenase digestion as an assay for collagen in partially synchronized secondary cultures of chick embryo fibroblasts, we find that the rate of collagen synthesis remains at a constant fraction of overall protein synthesis (5%) regardless of the growth rate of the cells even whe
## Abstract The mechanisms of tumor promotion in liver by various xenobiotics of diverse structure are not well understood. However, these tumor promoters share the ability to exert growth‐stimulatory effects on hepatocytes. Our laboratory has been utilizing normal rat hepatocytes under defined con
## Abstract Zebrafish SmyD1 is a SET and MYND domain‐containing protein that plays an important role in myofiber maturation and muscle contraction. SmyD1 is required for myofibril organization and sarcomere assembly during myofiber maturation. Whole‐mount in situ hybridization revealed that __smyd1