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J M Velazquez

Publications and source records attributed to J M Velazquez.

5 recordsLinked to original sources
PubMed1984

hsp70: nuclear concentration during environmental stress and cytoplasmic storage during recovery.

The intracellular distribution of the major Drosophila heat-shock protein hsp70 was determined by indirect immunofluorescence with monoclonal antibodies. During heat shock the protein concentrates strongly in nuclei while a small quantity remains cytoplasmic. During recovery hsp70 leaves the nuclei and becomes distributed throughout the cytoplasm. With a second heat shock it is rapidly transported back into the nucleus. Nuclear translocation depends not on the temperature per se, but on the physiological state of the cell since it also occurs after exposure to an anoxic atmosphere at normal temperatures. We also provide evidence that hsps protect cells from the toxic effects of anoxia, as well as heat, and conclude that nuclear translocation of hsp70 is related to its function in protecting the organism from both forms of environmental stress.

Animals↗
PubMed1983

Is the major Drosophila heat shock protein present in cells that have not been heat shocked?

When eukaryotic cells are exposed to elevated temperatures they respond by vigorously synthesizing a small group of proteins called the heat shock proteins. An essential element in defining the role of these proteins is determining whether they are unique to a stressed state or are also found in healthy, rapidly growing cells at normal temperatures. To date, there have been conflicting reports concerning the major heat-induced protein of Drosophila cells, HSP 70. We report the development of monoclonal antibodies specific for this protein. These antibodies were used to assay HSP 70 in cells incubated under different culture conditions. The protein was detectable in cells maintained at normal temperatures, but only when immunological techniques were pushed to the limits of their sensitivity. To test for the possibility that these cells contain a reservoir of protein in a cryptic antigenic state (i.e., waiting posttranslational modification for use at high temperature), we treated cells with cycloheximide or actinomycin D immediately before heat shock. HSP 70 was not detected in these cells. Finally, we tested for the presence of a reservoir of inactive messages by using a high stringency hybridization of 32P-labeled cloned gene sequences to electrophoretically separated RNAs. Although HSP 70 mRNA was detectable in rapidly growing cells, it was present at less than 1/1,000th the level achieved after induction.

Animals↗
PubMed1980

Intracellular localization of heat shock proteins in Drosophila.

When cells and tissues of Drosophila are subjected to elevated temperatures, the pattern of protein synthesis shifts from the production of a broad spectrum of different proteins to the vigorous production of a small number of new, heat shock proteins. The intracellular distribution of these proteins has been investigated through autoradiographic analysis of cells labeled with 3H-leucine at 23 degrees and 37 degrees C. After examining sections of cultured cells from D. melanogaster and polytene cells of D. virilis by electron and light microscopy, we conclude that little (if any) heat shock protein becomes associated with mitochondria, despite the many lines of evidence linking the response to respiratory stress. Confirming earlier reports on the presence of heat shock proteins in nuclei, we find the proteins are very highly concentrated there and that their transport to the nucleus occurs very rapidly. Interestingly, their free concentration in the nuclear sap is extremely low; they are, in fact, quantitatively associated with chromosomes. This association occurs in a nonrandom manner, their concentration in highly condensed chromatin being very low relative to that of other chromosomal loci.

Animals↗
PubMed1969

Alienation.

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