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Functional Identification of a Nuclear Localization Signal of MYB2 Protein in

机译:MYB2蛋白核定位信号的功能鉴定

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摘要

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.
机译:将MyB2蛋白质鉴定为在Giardia Lamblia中显示出心底膜诱导的表达的转录因子。虽然核导入对于转录因子的运作至关重要,但尚未确定G.Lamblia MyB2(GLMYB2)的明显核定位信号(NLS)。基于由2个程序预测的推定GLMYB2 NLS,构建了一系列表达来自G.LAMBLIA谷氨酸脱氢酶的启动子的血凝素(HA)的血糖蛋白的质粒。使用抗HA抗体的免疫荧光测定表明GLMYB2的核定位需要GLMYB2氨基酸序列#507-#530,该序列被命名为NLSGLMYB2。我们通过证明通过融合NlsGlMyB2和G.Lamblia甘油醛3-磷酸脱氢酶,非核蛋白质获得的蛋白质的核位置来验证了该发现。我们关于GLMYB2的数据将扩大我们对在G. Lamblia中运行的NLSS的理解。

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