spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by APPELS, R.
Right arrow Articles by WILLIAMS, A. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by APPELS, R.
Right arrow Articles by WILLIAMS, A. F.

Journal of Cell Science, Vol 10, 47-59, Copyright © 1972 by Company of Biologists

Submitted on June 10, 1971

Characterization of DNA-Bound Histone in the Cells of The Avian Erythropoietic Series

R. APPELS 1, J. R. E. WELLS 1, and A. F. WILLIAMS 2

1 Department of Biochemistry, University of Adelaide, Adelaide, South Australia 5001
2 Department of Biochemistry, University of Oxford, England

The distribution of DNA-bound histone from purified cell populations of the avian erythroid cell series was studied to examine the possible relationship between these molecules and the in vivo activity of cells. High-resolution polyacrylamide gel electrophoresis of histones indicated that the 3 main cell types, namely, erythrocytes (inactive in macromolecular synthesis), polychromatic erythrocytes (active in RNA and protein synthesis) and erythroblasts (dividing cells) all contained the same histone components. This result is contrary to previous reports that the f2c histone (characteristic of avian erythroid cells) was absent from erythroblasts; in addition it does not support the proposition that dividing cells contain a unique f1 histone component. Quantitation of histone analyses showed that erythroblasts contain relatively less f2c histone than the non-dividing cells of the series and that there was a slight redistribution of f1 histone components between polychromatic and mature erythrocytes.

Submitted on June 10, 1971







© The Company of Biologists Ltd 1972