Sperling J, Chebath J, Arad-Dann H, Offen D, Spann P, Lehrer R, Goldblatt D, Jolles B, Sperling R
Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, Israel.
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10377-81. doi: 10.1073/pnas.88.23.10377.
The first step in splicing of pre-mRNA involves an intermediate lariat structure, in which a 2'5' phosphodiester bond between the 5' terminal guanosine residue of the intron and a specific adenosine residue near the 3' end of the intron is formed. A mammalian enzyme that generates 2'-5' phosphodiester bonds is (2'-5')oligoadenylate synthetase [(2'-5')OASE]. Although the expression of this enzyme is induced by interferon, low constitutive levels can be detected in untreated cells and tissues. The structural similarity between the lariat branch point and the 2'-5' phosphodiester bond generated by (2'-5')OASE prompted the experiments described here which suggest that this enzyme is involved in pre-mRNA splicing. (i) We show that a (2'-5')OASE activity is associated with 60S spliceosomes in an ATP- and RNA-dependent manner and that it can be indirectly immunoprecipitated by anti-Sm antibodies. (ii) Antibodies against (2'-5')OASE inhibit the lariat formation in the first step of splicing when added directly to a splicing reaction in vitro. (iii) HeLa cell nuclear extracts immunodepleted of (2'-5')OASE activity were also deficient in splicing activity.
前体mRNA剪接的第一步涉及一个中间套索结构,其中内含子5'末端鸟苷残基与内含子3'末端附近的一个特定腺苷残基之间形成2'5'磷酸二酯键。一种能生成2'-5'磷酸二酯键的哺乳动物酶是(2'-5')寡腺苷酸合成酶[(2'-5')OASE]。虽然这种酶的表达受干扰素诱导,但在未处理的细胞和组织中可检测到低水平的组成性表达。套索分支点与(2'-5')OASE生成的2'-5'磷酸二酯键之间的结构相似性促使我们进行了此处所述的实验,这些实验表明该酶参与前体mRNA剪接。(i)我们发现(2'-5')OASE活性以ATP和RNA依赖的方式与60S剪接体相关,并且它可以被抗Sm抗体间接免疫沉淀。(ii)当直接添加到体外剪接反应中时,针对(2'-5')OASE的抗体在剪接的第一步抑制套索的形成。(iii)免疫去除了(2'-5')OASE活性的HeLa细胞核提取物在剪接活性方面也存在缺陷。