Bcl-2 differentially targets K-, N-, and H-Ras to mitochondria in IL-2 supplemented or deprived cells: implications in prevention of apoptosis. (Q40928348)

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scientific article published on September 1999

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English	Bcl-2 differentially targets K-, N-, and H-Ras to mitochondria in IL-2 supplemented or deprived cells: implications in prevention of apoptosis.	scientific article published on September 1999

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31 October 2019

Bcl-2 differentially targets K-, N-, and H-Ras to mitochondria in IL-2 supplemented or deprived cells: implications in prevention of apoptosis (English)

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31 October 2019

Dolores Pérez-Sala

2

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31 October 2019

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Rebollo A

1

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31 October 2019

Martínez-A C

3

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31 October 2019

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1 September 1999

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31 October 2019

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31 October 2019

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31 October 2019

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31 October 2019

4930-4939

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31 October 2019

Protein lipidation in cell signaling

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Ras signalling and apoptosis

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Bcl-2 associates with the ras-related protein R-ras p23

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Ras activation leads to cell proliferation or apoptotic cell death upon interleukin-2 stimulation or lymphokine deprivation, respectively

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Polylysine and CVIM sequences of K-RasB dictate specificity of prenylation and confer resistance to benzodiazepine peptidomimetic in vitro.

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Benzodiazepine peptidomimetics: potent inhibitors of Ras farnesylation in animal cells

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Ras-GRF activates Ha-Ras, but not N-Ras or K-Ras 4B, protein in vivo

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Isoprenoid addition to Ras protein is the critical modification for its membrane association and transforming activity

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Inhibition of the prenylation of K-Ras, but not H- or N-Ras, is highly resistant to CAAX peptidomimetics and requires both a farnesyltransferase and a geranylgeranyltransferase I inhibitor in human tumor cell lines

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Three distinct IL-2 signaling pathways mediated by bcl-2, c-myc, and lck cooperate in hematopoietic cell proliferation

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Inhibition of isoprenoid biosynthesis induces apoptosis in human promyelocytic HL-60 cells.

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High-affinity and intermediate-affinity forms of the human interleukin 2 receptor, expressed in an interleukin 9-dependent murine T cell line, deliver proliferative signals via differences in their transduction pathways

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Sequence requirement for peptide recognition by rat brain p21ras protein farnesyltransferase

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Evidence for a high affinity, saturable, prenylation-dependent p21Ha-ras binding site in plasma membranes

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Cloning of the gamma chain of the human IL-2 receptor

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Prenylation-dependent association of Ki-Ras with microtubules. Evidence for a role in subcellular trafficking

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Bcl-2 targets the protein kinase Raf-1 to mitochondria

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Protooncogene bcl-2 gene transfer abrogates Fas/APO-1 antibody-mediated apoptosis of human malignant glioma cells and confers resistance to chemotherapeutic drugs and therapeutic irradiation

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K- and N-Ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors

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The genetic regulation of apoptosis

1 reference

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Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked

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7 January 2021

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Role of protein modification reactions in programming interactions between ras-related GTPases and cell membranes

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Characterization of Ha-ras, N-ras, Ki-Ras4A, and Ki-Ras4B as in vitro substrates for farnesyl protein transferase and geranylgeranyl protein transferase type I

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based on heuristic

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Identifiers

10.1038/SJ.ONC.1202875

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490827%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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Europe PubMed Central

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31 October 2019

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