Hughes K, Ramakrishna S, Benjamin W B, Woodgett J R
Ludwig Institute for Cancer Research, London, U.K.
Biochem J. 1992 Nov 15;288 ( Pt 1)(Pt 1):309-14. doi: 10.1042/bj2880309.
Multifunctional ATP-citrate lyase kinase (ACLK) exhibits several properties that are similar to glycogen-synthase kinase-3 (GSK-3). The molecular cloning of two distinct mammalian GSK-3 cDNAs and a Drosophila melanogaster (fruitfly) homologue, zeste-white3sgg, has established the existence of a GSK-3 subfamily. A multifunctional protein kinase first identified as an ACLK has recently been shown to exhibit several similarities to the alpha- and beta-forms of GSK-3. Here we have used immunological and biochemical analyses to directly compare these enzymes. Thus purified preparations of ACLK isolated from brain and liver preferentially cross-react with anti-GSK-3 alpha antisera and phosphorylate previously defined substrates of GSK-3 at identical sites. Conversely, both alpha- and beta-forms of GSK-3 phosphorylated ATP-citrate lyase at the same site(s) targeted by ACLK. These, and other similarities, demonstrate ACLK to be identical with, or highly related to, GSK-3 alpha, the implications of which are discussed.
多功能ATP - 柠檬酸裂解酶激酶(ACLK)具有一些与糖原合酶激酶3(GSK - 3)相似的特性。两种不同的哺乳动物GSK - 3 cDNA以及果蝇同源物zeste - white3sgg的分子克隆证实了GSK - 3亚家族的存在。一种最初被鉴定为ACLK的多功能蛋白激酶最近被证明与GSK - 3的α和β形式有若干相似之处。在此,我们运用免疫学和生化分析方法直接比较这些酶。从脑和肝中分离得到的纯化ACLK制剂优先与抗GSK - 3α抗血清发生交叉反应,并在GSK - 3先前确定的底物的相同位点进行磷酸化。相反,GSK - 3的α和β形式都在ACLK靶向的相同位点对ATP - 柠檬酸裂解酶进行磷酸化。这些以及其他相似之处表明ACLK与GSK - 3α相同或高度相关,并对其意义进行了讨论。