Janus激酶3
突变
点突变
白细胞介素2
BETA(编程语言)
酪氨酸
受体
生物
化学
白细胞介素12
遗传学
生物化学
基因
体外
细胞毒性T细胞
程序设计语言
计算机科学
作者
Sarah M. Russell,James A. Johnston,Masayuki Noguchi,Masaru Kawamura,Chris M. Bacon,Michael Friedmann,Maria Berg,Daniel W. McVicar,Bruce A. Witthuhn,Olli Silvennoinen,Armond S. Goldman,Frank C. Schmalstieg,James N. Ihle,John J. O’Shea,Warren J. Leonard
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1994-11-11
卷期号:266 (5187): 1042-1045
被引量:647
标识
DOI:10.1126/science.7973658
摘要
Interleukin-2 (IL-2) signaling requires the dimerization of the IL-2 receptor β (IL-2Rβ) and common γ (γ c ) chains. Mutations of γ c can result in X-linked severe combined immunodeficiency (XSCID). IL-2, IL-4, IL-7 (whose receptors are known to contain γ c ), and IL-9 (whose receptor is shown here to contain γ c ) induced the tyrosine phosphorylation and activation of the Janus family tyrosine kinases Jak1 and Jak3. Jak1 and Jak3 associated with IL-2Rβ and γ c , respectively; IL-2 induced Jak3-IL-2Rβ and increased Jak3-γ c associations. Truncations of γ c , and a γ c , point mutation causing moderate X-linked combined immunodeficiency (XCID), decreased γ c -Jak3 association. Thus, γ c mutations in at least some XSCID and XCID patients prevent normal Jak3 activation, suggesting that mutations of Jak3 may result in an XSCID-like phenotype.
科研通智能强力驱动
Strongly Powered by AbleSci AI