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四膜虫含有两种独特且不同寻常的类高迁移率族(HMG)蛋白。

Tetrahymena contain two distinct and unusual high mobility group (HMG)-like proteins.

作者信息

Schulman I G, Cook R G, Richman R, Allis C D

出版信息

J Cell Biol. 1987 Jun;104(6):1485-94. doi: 10.1083/jcb.104.6.1485.

Abstract

Previous studies have described the existence of high mobility group (HMG)-like proteins in macronuclei of the ciliated protozoan, Tetrahymena thermophila (Hamana, K., and K. Iwai, 1979, J. Biochem. [Tokyo], 69:1097-1111; Levy-Wilson, B., M. S. Denker, and E. Ito, 1983, Biochemistry, 22:1715-1721). In this report, two of these proteins, LG-1 and LG-2, have been further characterized. Polyclonal antibodies raised against LG-1 and LG-2 fail to cross react with each other or any other macronuclear polypeptide in immunoblotting analyses. As well, LG-1 and LG-2 antibodies do not react with calf thymus, chicken, or yeast HMG proteins. Consistent with these results, a 47 amino-terminal sequence of LG-1 has been determined that shows limited homology to both calf thymus HMGs 1 and 2 and HMGs 14 and 17. Two internal sequences of V8 protease-generated peptides from LG-2 have been determined, and these do not share any homology to the LG-1 sequence or any other sequenced HMG proteins. Comparison of the partial sequences of LG-1 and LG-2 with the complete amino acid sequence of the Tetrahymena histone H1 (Wu, M., C. D. Allis, R. Richman, R. G. Cook, and M. A. Gorovsky, 1986, Proc. Natl. Acad. Sci. USA, 83:8674-8678) rules out the possibility that LG-1 and LG-2 are proteolytically derived from H1, the other major macronuclear perchloric acid-soluble protein. Interestingly, however, both LG-1 and LG-2 are efficiently extracted from macronuclei by elutive intercalation (Schröter, H., G. Maier, H. Ponsting, and A. Nordheim, 1985, Embo (Eur. Mol. Biol. Organ.) J., 4:3867-3872), suggesting that both may share yet undetermined properties with HMGs 14 and 17 of higher eukaryotes. Examination of the pattern of LG-1 and LG-2 synthesis during the sexual phase of the life cycle, conjugation, demonstrates that the synthesis of LG-1 and LG-2 is coordinately increased from basal levels during the differentiation of new macronuclei (7-13 h), suggesting that both of these proteins play a role in determining a macronuclear phenotype. However, a specific induction of LG-2 synthesis is detected in early stages of conjugation (meiotic prophase, 1-4 h), leading to maximal synthesis of LG-2 at 3 h. Interestingly, the early induction of LG-2 synthesis closely parallels the hyperphosphorylation of histone H1. Taken together, these data suggest that LG-1 and LG-2 are not strongly related to each other or to higher eukaryotic HMG proteins.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

先前的研究已描述了在纤毛原生动物嗜热栖热四膜虫的大核中存在高迁移率族(HMG)样蛋白(滨名,K.,和岩井,K.,1979年,《东京生物化学杂志》,69:1097 - 1111;利维 - 威尔逊,B.,M. S. 登克,和伊藤,E.,1983年,《生物化学》,22:1715 - 1721)。在本报告中,对其中两种蛋白LG - 1和LG - 2进行了进一步表征。在免疫印迹分析中,针对LG - 1和LG - 2产生的多克隆抗体彼此之间以及与任何其他大核多肽均无交叉反应。同样,LG - 1和LG - 2抗体与小牛胸腺、鸡或酵母的HMG蛋白也不发生反应。与这些结果一致,已确定LG - 1的47个氨基末端序列,该序列与小牛胸腺HMGs 1和2以及HMGs 14和17具有有限的同源性。已确定了来自LG - 2的V8蛋白酶产生的肽的两个内部序列,这些序列与LG - 1序列或任何其他已测序的HMG蛋白均无同源性。将LG - 1和LG - 2的部分序列与嗜热栖热四膜虫组蛋白H1的完整氨基酸序列(吴,M.,C. D. 阿利斯,R. 里奇曼,R. G. 库克,和M. A. 戈罗夫斯基,1986年,《美国国家科学院院刊》,83:8674 - 8678)进行比较,排除了LG - 1和LG - 2是从H1(另一种主要的大核高氯酸可溶性蛋白)经蛋白水解衍生而来的可能性。然而,有趣的是,LG - 1和LG - 2都可通过洗脱插入法(施罗特,H.,G. 迈尔,H. 庞斯汀,和A. 诺德海姆,1985年,《欧洲分子生物学组织杂志》,4:3867 - 3872)从大核中有效提取,这表明两者可能与高等真核生物的HMGs 14和17具有尚未确定的共同特性。对生命周期有性阶段(接合)期间LG - 1和LG - 2的合成模式进行检查表明,在新大核分化期间(7 - 13小时),LG - 1和LG - 2的合成从基础水平协同增加,这表明这两种蛋白在确定大核表型中均起作用。然而,在接合早期阶段(减数分裂前期,1 - 4小时)检测到LG - 2合成的特异性诱导,导致LG - 2在3小时时合成达到最大值。有趣的是,LG - 2合成的早期诱导与组蛋白H1的过度磷酸化密切平行。综上所述,这些数据表明LG - 1和LG - 2彼此之间以及与高等真核生物的HMG蛋白均无密切关系。(摘要截至于400字)

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