RNA synthesis almost ceases in mitosis. It is ambiguous whether this temporal, negative control of RNA synthesis is solely because of the nature of chromosomes per se, (i.e., their condensed state), or to a physical loss of RNA polymerases along with other nuclear proteins which have been shown to pass into the cytoplasm in mitosis, or to their combined feature. Aside from such regulatory considerations, a question has also been raised as to whether RNA polymerases are constituents of metaphase chromosomes. To clarify these aspects of RNA polymerase-chromatin interaction in mitosis, the enzymes in chromosomes were quantitated and their levels compared to those in interphase nuclei and cells at various phases of the cell cycle. The results show that the amounts of form I, form II, and probably form III enzymes bound to a genome-equivalent of chromatin stay constant during the cell cycle. Thus, the mechanism for the negative control of RNA synthesis in mitosis appears to exist in the chromosomes per se, but not to be directly related to the RNA polymerase levels. This quantitative conservation of chromatin-bound RNA polymerases implies that they may persist as structural components of the chromosomes in mitosis.
Skip Nav Destination
Article navigation
1 February 1979
Article|
February 01 1979
Quantitative conservation of chromatin-bound RNA polymerases I and II in mitosis. Implications for chromosome structure.
S I Matsui
H Weinfeld
A A Sandberg
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1979) 80 (2): 451–464.
Citation
S I Matsui, H Weinfeld, A A Sandberg; Quantitative conservation of chromatin-bound RNA polymerases I and II in mitosis. Implications for chromosome structure.. J Cell Biol 1 February 1979; 80 (2): 451–464. doi: https://doi.org/10.1083/jcb.80.2.451
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement