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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by DAVIES, H. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by DAVIES, H. G.

Journal of Cell Science, Vol 3, 129-150, Copyright © 1968 by Company of Biologists

Submitted on May 25, 1967

Electron-Microscope Observations on the Organization of Hetero-Chromatin in Certain Cells

H. G. DAVIES 1

1 Medical Research Council Biophysics Research Unit, King's College 26-29 Drury Lane, London, W.C.2

Electron micrographs of sections through the heterochromatin (condensed chromosomes) of erythrocytes from chicken and lamprey reveal alternate equispaced electron-dense and relatively less dense bands lying adjacent and parallel to, and extending considerable distances along, the nuclear envelope. Frequently a triple-structured band (average half-width 183 Å), consisting of a less dense band, a dense band (width 130-170 Å), and a second less dense band is encountered; sometimes there are many (10-12) bands. The dense bands have a variable structure; they may appear continuous or consist of equispaced granules about 220 Å apart, which sometimes have a less dense centre. Similar but shorter dark bands and granules appear throughout the chromatin. Tilting the section in the microscope causes the micrographs to change, bands and granules disappearing and reappearing elsewhere, demonstrating that the images are produced by superposition of structures small in dimensions compared with the thickness of the section. Tilting about an axis normal to the band may resolve it into granules. These data indicate that the heterochromatin contains a well-defined structural unit which can form ordered regions, namely layers in contact with the nuclear envelope. The possibility of errors in interpreting the substructure of the bands due to complexity of superposition effects is stressed. The simplest hypothesis to account for the images is that the units are microtubes of outside diameter 130-170 Å, perhaps microhelices formed by coiling DNA with protein, spaced apart equally, perhaps by spacing elements. Microtubes parallel to the optic axis would appear as hollow granules, several one above another in a plane parallel to the axis appearing as a dark band. A similar triple-structured band of average half-width 224 Å is found in cells from newt spleen, lymphocytes, polychromatophil erythroblasts, mature erythrocytes, basophilic granulocytes, reticular cells and macrophages. A survey of published micrographs shows a similar triple-structured band of average half-width 212 Å to be a common feature of many cell types. A triple-structured band probably gives rise to the sheets of chromatin, now shown to have a similar triple-layered structure, limited on both sides by nuclear envelope, previously found attached to interphase nuclei and mitotic chromosomes in certain polychromatic erythroblasts from the newt. The effects of tilting the section were studied on objects of known geometry, membranes and cytoplasmic microtubules.

Submitted on May 25, 1967




This article has been cited by other articles:


Home page
ScienceHome page
A. L. Olins and D. E. Olins
Spheroid Chromatin Units (ngr Bodies)
Science, January 25, 1974; 183(4122): 330 - 332.
[Abstract] [PDF]




© The Company of Biologists Ltd 1968