|
|
|
Research Papers
Istituto di Biologia Cellulare, C.N.R., Roma, Italy.
Abstract
Cloned gene for Xenopus ribosomal protein L1 was injected into fertilized eggs, and its expression was analyzed during the period of embryo development when the mRNAs produced by the endogenous ribosomal protein genes are still silent due to a translational control. The injected genes replicated extensively, and a 10-fold excess of L1 mature transcript accumulated in the embryo. This was accompanied by a small amount of incompletely processed L1 RNA that still contained one out of nine introns, a molecule never observed in normal conditions. The excess mature L1 mRNA was distributed between polysomes and messenger ribonucleoproteins (mRNPs) in the same relative proportion observed in control embryos of the same stage. Therefore, more L1 mRNA was loaded onto polysomes and caused the appearance of L1 protein when this was not yet detectable in control embryos. The results suggest a relationship between the excess amount of L1 protein and the alteration in processing of its transcripts.
This article has been cited by other articles:
![]() |
M L Hammond, W Merrick, and L H Bowman Sequences mediating the translation of mouse S16 ribosomal protein mRNA during myoblast differentiation and in vitro and possible control points for the in vitro translation. Genes & Dev., September 1, 1991; 5(9): 1723 - 1736. [Abstract] [PDF] |
||||
![]() |
Y F Tsay, J R Thompson, M O Rotenberg, J C Larkin, and J L Woolford Ribosomal protein synthesis is not regulated at the translational level in Saccharomyces cerevisiae: balanced accumulation of ribosomal proteins L16 and rp59 is mediated by turnover of excess protein. Genes & Dev., June 1, 1988; 2(6): 664 - 676. [Abstract] [PDF] |
||||