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 Risueno, M. C.
Right arrow Articles by Moreno Diaz de la Espina, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Risueno, M. C.
Right arrow Articles by Moreno Diaz de la Espina, S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Cell Science, Vol 58, Issue 1 313-329, Copyright © 1982 by Company of Biologists


JOURNAL ARTICLES

Nucleolar fibrillar centres in plant meristematic cells: ultrastructure, cytochemistry and autoradiography

MC Risueno, FJ Medina and S Moreno Diaz de la Espina

In plant cells nucleolar fibrillar centres (FCs) undergo ultrastructural changes, depending on the nucleolar activity. We have found two types of FC structure in nucleoli with either high or low activity, to which we have given the conventional names of homogeneous and heterogeneous, respectively. The first type is characterized by the presence of fibres that we describe structurally and cytochemically as decondensed chromatin; the second type, in addition to these fibres, contains a variable number of dense cores made up of condensed chromatin. Moreover, RNA does not appear to be present in FCs, while proteins are a major component. Autoradiography after tritiated uridine incorporation shows that FCs are not the site of transcription, but that this takes place in the fibrillar component; the same result is obtained using the lead acetate fixation technique for detecting orthophosphate ions. This fact leads us to think that FCs are not the whole interphasic counterpart of the mitotic nucleolar organizing region (NOR), as stated by other authors, but only the portion of the NOR that is temporarily inactive in transcription; the transcriptionally active part of the NOR is in the fibrillar component, bound to its earliest product of transcription. Thus, FCs and the fibrillar component constitute a functional unit.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
T. Wei, H. Baiqu, L. Chunxiang, and Z. Zhonghe
In situ visualization of rDNA arrangement and its relationship with subnucleolar structural regions in Allium sativum cell nucleolus
J. Cell Sci., March 15, 2003; 116(6): 1117 - 1125.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A Olmedilla, P. Testillano, O Vicente, M Delseny, and M. Risueno
Ultrastructural rRNA localization in plant cell nucleoli. RNA/RNA in situ hybridization, autoradiography and cytochemistry
J. Cell Sci., January 12, 1993; 106(4): 1333 - 1346.
[Abstract] [PDF]




© The Company of Biologists Ltd 1982