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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1990-01-12
    Description: Normal cells in culture invariably undergo senescence, whereby they cease proliferation after a finite number of doublings. Irreversible changes in gene expression occurred in senescent human fetal lung fibroblasts: a non-cell cycle-regulated mRNA was partially repressed; an unusual polyadenylated histone mRNA was expressed; although serum induced c-H-ras, c-myc, and ornithine decarboxylase mRNA normally, ornithine decarboxylase activity was deficient; and serum did not induce mRNA for a replication-dependent histone and for the c-fos proto-oncogene. The loss of c-fos inducibility was the result of a specific, transcriptional block. The results suggest that senescent fibroblasts were unable to proliferate because of, at least in part, selective repression of c-fos; moreover, the multiple changes in gene expression support the view that cellular senescence is a process of terminal differentiation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seshadri, T -- Campisi, J -- AG07114/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1990 Jan 12;247(4939):205-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Boston University Medical School, MA 02118.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2104680" target="_blank"〉PubMed〈/a〉
    Keywords: Blood ; Cell Division ; Cell Line ; Cell Survival/physiology ; Embryo, Mammalian ; Fibroblasts/*cytology/metabolism ; Gene Expression/*physiology ; Humans ; Ornithine Decarboxylase/genetics ; Proto-Oncogene Proteins/*genetics ; Proto-Oncogene Proteins c-fos ; Proto-Oncogene Proteins c-myc ; Proto-Oncogene Proteins p21(ras) ; RNA, Messenger/biosynthesis/genetics ; *Suppression, Genetic ; *Transcription, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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