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Nuclear organisation and gene expression
Current Opinion in Cell Biology, 2002The development of increasingly sophisticated tools to track chromosomes and proteins in living cells offers the possibility of visualising gene regulation in the nucleus with minimal distortion. This, in conjunction with powerful genetic approaches available in yeast, is beginning to allow functional definition of nuclear "compartments".
Jonathan, Baxter +2 more
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Nuclear genes in mitochondrial disorders
Current Opinion in Genetics & Development, 2003Nuclear genes encode hundreds of proteins involved in mitochondrial biogenesis and oxidative phosphorylation (OXPHOS). Nevertheless, the identification of nuclear genes responsible for OXPHOS-related disorders has proceeded at a much slower pace, compared with the discovery and characterization of mtDNA mutations.
Zeviani M., Spinazzola A., Carelli V.
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Nuclear compartments and gene regulation
Current Opinion in Genetics & Development, 1999Improvements in fluorescence microscopy have allowed us to explore the three-dimensional organization of the nucleus in ways that were impossible ten years ago, revealing subdomains or compartments within the nucleus defined by their enrichments of subsets of factors.
M, Cockell, S M, Gasser
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Nuclear compartmentalization and gene activity
Nature Reviews Molecular Cell Biology, 2000The regulated expression of genes during development and differentiation is influenced by the availability of regulatory proteins and accessibility of the DNA to the transcriptional apparatus. There is growing evidence that the transcriptional activity of genes is influenced by nuclear organization, which itself changes during differentiation.
C, Francastel +3 more
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Nuclear Organization and Gene Expression
Experimental Cell Research, 1996In actively transcribing cells, factors involved in pre-mRNA splicing localize in a speckled pattern at the fluorescence microscopic level. The speckled pattern corresponds to interchromatin granule clusters and perichromatin fibrils at the electron microscopic level. Based upon [3H]uridine incorporation studies transcription is thought to occur at the
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Gene-gene coordination by the nuclear envelope
Medical Hypotheses, 1995The paper studies how certain topologic features of the nuclear envelope may reorganize entrained transcription via spatial rearrangements of genes carried by distinct chromatids.
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Tetrapyrrole regulation of nuclear gene expression
Photosynthesis Research, 2002Tetrapyrroles are the structural backbone of chlorophyll and heme, and are essential for primary photochemistry, light harvesting, and electron transport. The biochemistry of their synthesis has been studied extensively, and it has been suggested that some of the tetrapyrrole biochemical intermediates can affect nuclear gene expression. In this review,
Judy A, Brusslan, Michael P, Peterson
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THE NUCLEAR HORMONE RECEPTOR GENE SUPERFAMILY
Annual Review of Medicine, 1995▪ Abstract The nuclear hormone receptor gene superfamily encodes structurally related proteins that regulate transcription of target genes. These macromolecules include receptors for steroid and thyroid hormones, vitamins, and other proteins for which no ligands have been found. These receptors have modular domains. The DNA-binding domain directs the
R C, Ribeiro, P J, Kushner, J D, Baxter
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Artificial modification of nuclear gene activity
International Journal of Biochemistry, 1981Abstract 1. 1. Various experimental systems in which nuclear gene activity may be artificially modified are discussed and compared. 2. 2. The experimental systems discussed include the construction of hybrid cells by heterokaryon formation, or nuclear transplantation techniques; the injection of cell extracts into cells; and various cell-free
S P, Gregory +2 more
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Searching for nuclear-mitochondrial genes
Trends in Genetics, 2003Recently, a novel strategy has been developed to identify yeast genes that are important for mitochondrial respiratory chain function. This approach found a large number of genes that were not previously thought to be involved, providing new candidate disease genes for mitochondrial disorders.
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