Department of Environmental Medical Biology and Institute of Tropical Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.
Korean J Parasitol. 2020 Dec;58(6):675-679. doi: 10.3347/kjp.2020.58.6.675. Epub 2020 Dec 29.
MYB2 protein was identified as a transcription factor that showed encystation-induced expression in Giardia lamblia. Although nuclear import is essential for the functioning of a transcription factor, an evident nuclear localization signal (NLS) of G. lamblia MYB2 (GlMYB2) has not been defined. Based on putative GlMYB2 NLSs predicted by 2 programs, a series of plasmids expressing hemagglutinin (HA)-tagged GlMYB2 from the promoter of G. lamblia glutamate dehydrogenase were constructed and transfected into Giardia trophozoites. Immunofluorescence assays using anti-HA antibodies indicated that GlMYB2 amino acid sequence #507-#530 was required for the nuclear localization of GlMYB2, and this sequence was named as NLSGlMYB2. We further verified this finding by demonstrating the nuclear location of a protein obtained by the fusion of NLSGlMYB2 and G. lamblia glyceraldehyde 3-phosphate dehydrogenase, a non-nuclear protein. Our data on GlMYB2 will expand our understanding on NLSs functioning in G. lamblia.
MYB2 蛋白被鉴定为一种转录因子,在蓝氏贾第鞭毛虫中表现出囊形成诱导表达。尽管核输入对于转录因子的功能至关重要,但蓝氏贾第鞭毛虫 MYB2(GlMYB2)的明显核定位信号(NLS)尚未确定。基于两个程序预测的假定 GlMYB2 NLS,构建了一系列表达来自蓝氏贾第鞭毛虫谷氨酸脱氢酶启动子的 HA 标记 GlMYB2 的质粒,并转染到贾第虫滋养体中。使用抗 HA 抗体的免疫荧光分析表明,GlMYB2 氨基酸序列 #507-#530 是 GlMYB2 核定位所必需的,该序列被命名为 NLSGlMYB2。我们通过证明融合了 NLSGlMYB2 和蓝氏贾第鞭毛虫 3-磷酸甘油醛脱氢酶的蛋白质的核定位进一步验证了这一发现,该蛋白质是一种非核蛋白。我们关于 GlMYB2 的数据将扩展我们对蓝氏贾第鞭毛虫中 NLS 功能的理解。