Knight Andrea, Piskacek Martin
Department of Pathological Physiology, Faculty of Medicine, Masaryk University Brno, Kamenice 5, 625 00, Brno, Czech Republic.
Department of Pathological Physiology, Faculty of Medicine, Masaryk University Brno, Kamenice 5, 625 00, Brno, Czech Republic.
Biochimie. 2022 Sep;200:19-26. doi: 10.1016/j.biochi.2022.05.004. Epub 2022 May 10.
Previously, the Nine amino acid TransActivation Domain (9aaTAD) was identified in the Gal4 region 862-870 (DDVYNYLFD). Here, we identified 9aaTADs in the distal Gal4 orthologs by our prediction algorithm and found their conservation in the family. The 9aaTAD function as strong activators was demonstrated. We identified adjacent Gal4 region 871-811 (DEDTPPNPKKE) as a natural 9aaTAD inhibitory domain located at the extreme Gal4 terminus. Moreover, we identified conserved Gal4 region 172-185 (FDWSEEDDMSDGLP), which was capable to reverse the 9aaTAD inhibition. In conclusion, our results uncover the existence of the cryptic inhibitory domains, which need to be carefully implemented in all functional studies with transcription factors to avoid incorrect conclusions.
此前,在Gal4区域862 - 870(DDVYNYLFD)中鉴定出九氨基酸反式激活结构域(9aaTAD)。在此,我们通过预测算法在远端Gal4直系同源物中鉴定出9aaTAD,并发现它们在该家族中的保守性。9aaTAD作为强激活剂的功能得到了证实。我们将相邻的Gal4区域871 - 811(DEDTPPNPKKE)鉴定为位于Gal4极端末端的天然9aaTAD抑制结构域。此外,我们鉴定出保守的Gal4区域172 - 185(FDWSEEDDMSDGLP),其能够逆转9aaTAD的抑制作用。总之,我们的结果揭示了隐藏抑制结构域的存在,在所有涉及转录因子的功能研究中都需要谨慎考虑,以避免得出错误结论。