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Involvement of the ...
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Wang, X.Department of Immunology, Burnham Institute, San Diego, CA 92037, United States
(author)
Involvement of the MKK6-p38? cascade in ?-radiation-induced cell cycle arrest
- Article/chapterEnglish2000
Publisher, publication year, extent ...
Numbers
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LIBRIS-ID:oai:DiVA.org:liu-47626
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https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-47626URI
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https://doi.org/10.1128/MCB.20.13.4543-4552.2000DOI
Supplementary language notes
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Language:English
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Summary in:English
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Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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The p38 group of kinases belongs to the mitogen-activated protein (MAP) kinase superfamily with structural and functional characteristics distinguishable from those of the ERK, JNK (SAPK), and BMK (ERK5) kinases. Although there is a high degree of similarity among members of the p38 group in terms of structure and activation, each member appears to have a unique function. Here we show that activation of p38-? (also known as ERK6 or SAPK3), but not the other p38 isoforms, is required for ?-irradiation- induced G2 arrest. Activation of the MKK6-p38? cascade is sufficient to induce G2 arrest in cells, and expression of dominant negative alleles of MKK6 or p38? allows cells to escape the DNA damage-induce G2 delay. Activation of p38? is dependent on ATM and leads to activation of Cds1 (also known as Chk2). These data suggest a model in which activation of ATM by ? irradiation leads to the activation of MKK6, p38?, and Cds1 and that activation of both MKK6 and p38? is essential for the proper regulation of the G2 checkpoint in mammalian cells.
Subject headings and genre
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NATURAL SCIENCES
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NATURVETENSKAP
Added entries (persons, corporate bodies, meetings, titles ...)
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McGowan, C.H.Department of Molecular Biology, Burnham Institute, San Diego, CA 92037, United States
(author)
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Zhao, M.Department of Immunology, Burnham Institute, San Diego, CA 92037, United States, Department of Pathology, Linkoping University, S-581 85 Linkoping, Sweden
(author)
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He, L.Scripps Research Institute, Prog. Oncogenes Tum. Suppressor G., Burnham Institute, San Diego, CA 92037, United States
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Downey, J.S.Department of Immunology, Burnham Institute, San Diego, CA 92037, United States
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Fearns, C.Department of Immunology, Burnham Institute, San Diego, CA 92037, United States
(author)
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Wang, Y.Department of Physiology, Univ. of Maryland School of Medicine, Baltimore, MD 21201, United States
(author)
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Huang, S.Scripps Research Institute, Prog. Oncogenes Tum. Suppressor G., Burnham Institute, San Diego, CA 92037, United States
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Han, J.Department of Immunology, Burnham Institute, San Diego, CA 92037, United States, Department of Immunology, Scripps Research Institute, 10550 N. Torrey Pines Road, San Diego, CA 92037, United States
(author)
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Department of Immunology, Burnham Institute, San Diego, CA 92037, United StatesDepartment of Molecular Biology, Burnham Institute, San Diego, CA 92037, United States
(creator_code:org_t)
Related titles
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In:Molecular and Cellular Biology20:13, s. 4543-45520270-73061098-5549
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