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71.
To further our understanding of initiation and imprinting of X-chromosome inactivation, we have examined methylation of specific CpG sites of X-linked Pgk-1 and G6pd genes throughout female mouse development. Methylation occurs around the time of inactivation and earlier for Pgk-1, which is closer to the X-inactivation centre. In female primordial germ cells, the inactive X chromosome escapes methylation; this may underly the reversibility of inactivation at meiosis. Similarly, the genes are unmethylated on the inactive X chromosome in sperm; hence, the imprint specifying preferential X-inactivation in extra-embryonic tissues must reside elsewhere. 相似文献
72.
Long-term potentiation in the hippocampus is blocked by tyrosine kinase inhibitors. 总被引:37,自引:0,他引:37
Long-term potentiation (LTP) in the hippocampus is thought to contribute to memory formation. In the Ca1 region, LTP requires the NMDA (N-methyl-D-aspartate) receptor-dependent influx of Ca2+ and activation of serine and threonine protein kinases. Because of the high amount of protein tyrosine kinases in hippocampus and cerebellum, two regions implicated in learning and memory, we examined the possible additional requirement of tyrosine kinase activity in LTP. We first examined the specificity in brain of five inhibitors of tyrosine kinase and found that two of them, lavendustin A and genistein, showed substantially greater specificity for tyrosine kinase from hippocampus than for three serine-threonine kinases: protein kinase A, protein kinase C, and Ca2+/calmodulin kinase II. Lavendustin A and genistein selectively blocked the induction of LTP when applied in the bath or injected into the postsynaptic cell. By contrast, the inhibitors had no effect on the established LTP, on normal synaptic transmission, or on the neurotransmitter actions attributable to the actions of protein kinase A or protein kinase C. These data suggest that tyrosine kinase activity could be required postsynaptically for long-term synaptic plasticity in the hippocampus. As Ca2+ calmodulin kinase II or protein kinase C seem also to be required, the tyrosine kinases could participate postsynaptically in a kinase network together with serine and threonine kinases. 相似文献
73.
E. A. Meighen K. N. Slessor G. G. Grant 《Cellular and molecular life sciences : CMLS》1981,37(6):555-557
Summary Aldehyde dependent bacterial luciferases respond quantitatively to ng quantities of aldehyde pheromones from insects. The luminescent response is the basis for a quantitative assay used to analyse sex pheromone from several sources including individual female moths.This investigation was supported by a U.S.D.A. Forest Service Program entitled Canada United States Spruce Budworms Program (23–345) and the Medical Research Council of Canada (MT-4314). 相似文献
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G. Grant 《Cellular and molecular life sciences : CMLS》1965,21(12):722-723
Zusammenfassung Im Zusammenhang mit Untersuchungen an jungen Katzen über den Effekt der Durchschneidung von Axonen sind in Nauta-Präparaten zum ersten Mal am zentralen Teil der Neurone degenerierende Dendriten gefunden worden. Die Bedeutung dieses Befundes wird kurz diskutiert. 相似文献
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Sheen VL Ganesh VS Topcu M Sebire G Bodell A Hill RS Grant PE Shugart YY Imitola J Khoury SJ Guerrini R Walsh CA 《Nature genetics》2004,36(1):69-76
Disruption of human neural precursor proliferation can give rise to a small brain (microcephaly), and failure of neurons to migrate properly can lead to an abnormal arrest of cerebral cortical neurons in proliferative zones near the lateral ventricles (periventricular heterotopia). Here we show that an autosomal recessive condition characterized by microcephaly and periventricular heterotopia maps to chromosome 20 and is caused by mutations in the gene ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2). By northern-blot analysis, we found that mouse Arfgef2 mRNA levels are highest during embryonic periods of ongoing neuronal proliferation and migration, and by in situ hybridization, we found that the mRNA is widely distributed throughout the embryonic central nervous system (CNS). ARFGEF2 encodes the large (>200 kDa) brefeldin A (BFA)-inhibited GEF2 protein (BIG2), which is required for vesicle and membrane trafficking from the trans-Golgi network (TGN). Inhibition of BIG2 by BFA, or by a dominant negative ARFGEF2 cDNA, decreases cell proliferation in vitro, suggesting a cell-autonomous regulation of neural expansion. Inhibition of BIG2 also disturbed the intracellular localization of such molecules as E-cadherin and beta-catenin by preventing their transport from the Golgi apparatus to the cell surface. Our findings show that vesicle trafficking is an important regulator of proliferation and migration during human cerebral cortical development. 相似文献
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Trichodermin resistance--mutation affecting eukaryotic ribosomes 总被引:13,自引:0,他引:13