Chiang Y, Vishwanatha J K
Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, USA.
Mol Cell Biochem. 1996 Feb 23;155(2):131-8. doi: 10.1007/BF00229310.
Human Alu-elements are short interspersed DNA sequences that comprise approximately 5% of the human genome. The physiological role of Alu-elements are unknown, although they are proposed to be involved in DNA replication, transcriptional regulation and nuclear transport of signal recognition particle RNA. Proteins that bind to Alu-element and Alu RNA have been identified in human cells. In HeLa cells, two proteins of 120 kDa and 35 kDa specifically bind to Alu-elements. We find that the 35 kDa protein is localized exclusively to the nucleus, while the 120 kDa protein is distributed between nucleus and cytoplasm. The 35 kDa protein is regulated by phosphorylation. Upon dephosphorylation, its DNA binding activity is significantly enhanced. Contrary to the recent identification of the smaller Alu-element binding protein as annexin II, we find that annexin II is not an Alu-element binding protein. Using a variety of techniques, we demonstrate that the 35 kDa Alu-element binding protein is distinct from annexin II.
人类Alu元件是短散布DNA序列,约占人类基因组的5%。Alu元件的生理作用尚不清楚,尽管有人提出它们参与DNA复制、转录调控以及信号识别颗粒RNA的核运输。在人类细胞中已鉴定出与Alu元件和Alu RNA结合的蛋白质。在HeLa细胞中,两种分别为120 kDa和35 kDa的蛋白质特异性结合Alu元件。我们发现,35 kDa的蛋白质仅定位于细胞核,而120 kDa的蛋白质分布于细胞核和细胞质之间。35 kDa的蛋白质受磷酸化调节。去磷酸化后,其DNA结合活性显著增强。与最近将较小的Alu元件结合蛋白鉴定为膜联蛋白II相反,我们发现膜联蛋白II不是Alu元件结合蛋白。通过各种技术,我们证明35 kDa的Alu元件结合蛋白与膜联蛋白II不同。