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Nuclear ribosomal genes

Doyle JJ, Brown AHD (1989) 5S nuclear ribosomal gene variation in the Glycine tomentella polyploid complex (Leguminosae). Syst Bot 14 398-407... [Pg.114]

The gene encoding the smallest structural RNA component of the nuclear ribosome is the 5S rRNA gene. This gene is not co-located with the remaining nuclear rRNA genes. Neither sequence nor chromosomal location of the 5S gene is known for any neodermatan and it will not be discussed further here. [Pg.98]

Mitochondrial ribosomal genes are much smaller than even their bacterial homologues. Expansion segments found in nuclear ortho-logues are, of course, absent. Gerbi (1996) referred to contraction segments as features found in the bacterium E. coli that are absent from other rRNAs, particularly mt rRNAs. The... [Pg.115]

Ribosomal DNA gene transcription and ribosome assembly occur in the nucleolus, a highly specialized nuclear compartment. Quantitatively, the ribosomal gene transcription accounts for about 40% of all cellular transcription in living cells. These numbers reflect the relevance of this process for cell function and support the notion that regulation RNA Pol I transcription represents a key step in ribosome production and in determining a cell s potential for growth and proliferation (Larson et al., 1991 Nurse, 1985). [Pg.124]

Although we will stick to the IL-6 gene, it should be mentioned at the side that two other RNA polymerases exist in mammalian cells responsible for the synthesis of RNA molecules, which are not translated into proteins ribosomal (rRNA), transfer (tRNA), small nuclear (snRNA), small nucleolar (snoRNA), and some of the recently discovered microRNAs and piRNAs. These RNA molecules act in the process of translation and mRNA turnover. Micro and piRNAs are probably extremely important in the definition of stem cells and of differentiation programs. Some of them are synthesized by RNA polymerase II. [Pg.1225]

The majority of the peptides in mitochondria (about 54 out of 67) are coded by nuclear genes. The rest are coded by genes found in mitochondrial (mt) DNA. Human mitochondria contain two to ten copies of a smaU circular double-stranded DNA molecule that makes up approximately 1% of total ceUular DNA. This mtDNA codes for mt ribosomal and transfer RNAs and for 13 proteins that play key roles in the respiratory chain. The linearized strucmral map of the human mitochondrial genes is shown in Figure 36-8. Some of the feamres of mtDNA are shown in Table... [Pg.322]

Not all the cellular DNA is in the nucleus some is found in the mitochondria. In addition, mitochondria contain RNA as well as several enzymes used for protein synthesis. Interestingly, mitochond-rial RNA and DNA bear a closer resemblance to the nucleic acid of bacterial cells than they do to animal cells. For example, the rather small DNA molecule of the mitochondrion is circular and does not form nucleosomes. Its information is contained in approximately 16,500 nucleotides that func-tion in the synthesis of two ribosomal and 22 transfer RNAs (tRNAs). In addition, mitochondrial DNA codes for the synthesis of 13 proteins, all components of the respiratory chain and the oxidative phosphorylation system. Still, mitochondrial DNA does not contain sufficient information for the synthesis of all mitochondrial proteins most are coded by nuclear genes. Most mitochondrial proteins are synthesized in the cytosol from nuclear-derived messenger RNAs (mRNAs) and then transported into the mito-chondria, where they contribute to both the structural and the functional elements of this organelle. Because mitochondria are inherited cytoplasmically, an individual does not necessarily receive mitochondrial nucleic acid equally from each parent. In fact, mito-chondria are inherited maternally. [Pg.220]

S, 5S and 4.5S rRNAs) and a small 30S subunit (containing 16S rRNA). Chloro-plast ribosomal proteins are encoded by both nuclear and chloroplast genes. [Pg.45]

The Xenopus transcription factor IIIA not only acts as an essential RNA polymerase transcription factor for the expression of the 5S rRNA gene, it also binds to the 5S rRNA to form a 7S ribonucleoprotein particle that stabilizes the RNA until it is required for ribosome assembly and facilitates nuclear export of the 5S rRNA. Indeed, it was originally shown to be the protein component associated with 5S rRNA in the 7S particle in Xenopus oocytes before it was recognized as a transcription factor. How, we may ask, can this protein not only recognize specific DNA sequences in the 5S rRNA gene upstream region, but also recognize different, but equally specific, sequences in 5S rRNA ... [Pg.209]

Mitochondrial proteins encoded by nuclear genes are translated by ribosomes free in the cytoplasm, then folded and transferred into the mitochondria by different molecular chaperones. [Pg.55]

Molecular communication between the nucleus and the cytosol requires the movement of macromolecules through nuclear pores. RNA molecules synthesized in the nucleus are exported to the cytosol. Ribosomal proteins synthesized on cytosolic ribosomes are imported into the nucleus and assembled into 60S and 40S ribosomal subunits in the nucleolus completed subunits are then exported back to the cytosol. A variety of nuclear proteins (RNA and DNA polymerases, histones, topo-isomerases, proteins that regulate gene expression, and so forth) are synthesized in the cytosol and imported into the nucleus. This traffic is modulated by a complex system of molecular signals and transport proteins that is gradually being elucidated. [Pg.1071]


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