Neumann Brent, Zhao Liang, Murphy Kathleen, Gonda Thomas J
University of Queensland Diamantina Institute for Cancer, Immunology and Metabolic Medicine, Level 4, R-Wing, Building 1, Princess Alexandra Hospital, Brisbane, Qld. 4102, Australia.
Biochem Biophys Res Commun. 2008 May 23;370(1):62-6. doi: 10.1016/j.bbrc.2008.03.032. Epub 2008 Mar 18.
Although the first members of the Schlafen gene family were first described almost 10 years ago, the precise molecular/biochemical functions of the proteins they encode still remain largely unknown. Roles in cell growth, haematopoietic cell differentiation, and T cell development/maturation have, with some experimental support, been postulated, but none have been conclusively verified. Here, we have determined the subcellular localization of Schlafens 1, 2, 4, 5, 8, and 9, representing all three of the murine subgroups. We show that the proteins from subgroups I and II localize to the cytoplasm, while the longer forms in subgroup III localize exclusively to the nuclear compartment. We also demonstrate upregulation of Schlafen2 upon differentiation of haematopoietic cells and show this endogenous protein localizes to the cytoplasm. Thus, we propose the different subgroups of Schlafen proteins are likely to have functionally distinct roles, reflecting their differing localizations within the cell.
尽管Schlafen基因家族的首批成员在近10年前就首次被描述,但它们所编码蛋白质的确切分子/生化功能在很大程度上仍不清楚。在细胞生长、造血细胞分化以及T细胞发育/成熟过程中的作用,虽有一些实验支持,但尚未得到最终证实。在此,我们确定了代表小鼠所有三个亚组的Schlafen 1、2、4、5、8和9的亚细胞定位。我们发现,亚组I和II的蛋白质定位于细胞质,而亚组III中较长形式的蛋白质则仅定位于核区室。我们还证明了造血细胞分化时Schlafen2的上调,并表明这种内源性蛋白质定位于细胞质。因此,我们认为Schlafen蛋白质的不同亚组可能具有功能上不同的作用,这反映了它们在细胞内不同的定位。