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Michael E. Lee

Researcher at University of California, Berkeley

Publications -  8
Citations -  2059

Michael E. Lee is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: CRISPR & Gene. The author has an hindex of 5, co-authored 8 publications receiving 1666 citations. Previous affiliations of Michael E. Lee include Energy Biosciences Institute.

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Engineering Complex Synthetic Transcriptional Programs with CRISPR RNA Scaffolds

TL;DR: By extending guide RNAs to include effector protein recruitment sites, this work constructs modular scaffold RNAs that encode both target locus and regulatory action and applies this approach to flexibly redirect flux through a complex branched metabolic pathway in yeast.
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A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly

TL;DR: A versatile engineering platform for yeast, which contains both a rapid, modular assembly method and a basic set of characterized parts, and genome-editing tools for making modifications directly to the yeast chromosomes, which the authors find preferable to plasmids due to reduced variability in expression.
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Selection of chromosomal DNA libraries using a multiplex CRISPR system

TL;DR: Mutations recovered in the best cellodextrin transporters reveal synergy between substrate binding and transporter dynamics, and demonstrate the power of CRISPRm to accelerate selection experiments and discoveries of the molecular determinants that enhance biomolecule function.
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Expression-level optimization of a multi-enzyme pathway in the absence of a high-throughput assay

TL;DR: This work characterized a set of constitutive promoters in Saccharomyces cerevisiae that spanned a wide range of expression and maintained their relative strengths irrespective of the coding sequence and trained a regression model on a random sample comprising 3% of the total library, and used that model to predict genotypes that would preferentially produce each of the products in this highly branched pathway.
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Employing a combinatorial expression approach to characterize xylose utilization in Saccharomyces cerevisiae

TL;DR: Differences in promoter enrichment for the three-gene library depending on whether the pentose phosphate pathway genes were included during the aerobic enrichment are observed and the importance of selection conditions is observed.