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首页> 外文期刊>Science Advances >Accelerated evolution of a minimal 63–amino acid dual transcription factor
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Accelerated evolution of a minimal 63–amino acid dual transcription factor

机译:最小63氨基酸双转录因子的加速演变

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Transcription factors control gene expression in all life. This raises the question of what is the smallest protein that can support such activity. In nature, Cro from bacteriophage λ is one of the smallest known repressors (66 amino acids), and activators are typically much larger (e.g., λ cI, 237 amino acids). Previous efforts to engineer a minimal activator from λ Cro resulted in no activity in vivo in cells. In this study, we show that directed evolution results in a new Cro activator-repressor that functions as efficiently as λ cI in vivo. To achieve this, we develop phagemid-assisted continuous evolution (PACEmid). We find that a peptide as small as 63 amino acids functions efficiently as an activator and/or repressor. To our knowledge, this is the smallest protein activator that enables polymerase recruitment, highlighting the capacity of transcription factors to evolve from very short peptide sequences.
机译:转录因子对所有生命中的基因表达。这提出了可以支持此类活动的最小蛋白质的问题。本质上,来自噬菌体λ的CRO是最小的已知阻遏物(66个氨基酸)之一,并且活化剂通常更大(例如,λCI,237个氨基酸)。以往努力从λCro工程到最小的活化剂导致细胞中的体内没有活性。在这项研究中,我们表明,在新的CRO激活因子 - 压缩机中,导致的进化结果在体内以λCI有效地起作用。为此,我们开发噬事事辅助的连续演进(羽毛)。我们发现一只小于63氨基酸的肽作为活化剂和/或阻遏物有效地官能。据我们所知,这是最小的蛋白质活化剂,使聚合酶募集能够突出转录因子能力从非常短的肽序列中发展。

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