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Past research reports have created listings of a large number of potential target genes and contending models of HY5 transcription legislation. In this work, we execute step-by-step phenotypic and molecular analysis of constitutive activator and repressor HY5 fusion proteins. Applying this strategy, we had been in a position to filter more and more genetics which can be unlikely is direct targets, allowing us to get rid of several proposed different types of HY5's method of
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