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在诱导发生凋亡的锥虫以及自然发生的终末分化形式中,禁止素和RACK同源物上调。

Prohibitin and RACK homologues are up-regulated in trypanosomes induced to undergo apoptosis and in naturally occurring terminally differentiated forms.

作者信息

Welburn S C, Murphy N B

机构信息

Tsetse Research Group, Division of Molecular Genetics, Institute of Biomedical and Life Sciences, University of Glasgow, 56 Dumbarton Road, Glasgow G11 6NU, UK.

出版信息

Cell Death Differ. 1998 Jul;5(7):615-22. doi: 10.1038/sj.cdd.4400393.

Abstract

Two genes have been identified as up-regulated late during ConA-induced apoptosis in procyclic form Trypanosoma brucei rhodesiense. The first represents a homologue of prohibitin, a proto-oncogene originally described in mammals and subsequently in yeast, which is involved in cell-cycle control and senescence. The Trypanosoma prohibitin homologue appears to contain within it a putative death domain. The second gene, homologous to a family of regulatory proteins which are receptors for activated protein kinase C (RACKs), is also shown to be up-regulated in terminally differentiated bloodstream form trypanosomes. These are the first endogenous genes to be identified as up-regulated in programmed cell death (PCD) in unicellular organisms.

摘要

在罗得西亚布氏锥虫前循环型中,有两个基因被鉴定为在刀豆球蛋白A诱导的凋亡后期上调。第一个基因是一种禁阻蛋白的同源物,禁阻蛋白是一种原癌基因,最初在哺乳动物中发现,随后在酵母中也有发现,它参与细胞周期调控和衰老过程。锥虫的禁阻蛋白同源物似乎包含一个推定的死亡结构域。第二个基因与一类调节蛋白家族同源,这类调节蛋白是活化蛋白激酶C(RACKs)的受体,在终末分化的血流型锥虫中也显示出上调。这些是在单细胞生物程序性细胞死亡(PCD)中被鉴定为上调的首批内源性基因。

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