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TUNEYALI Library
(Pooled Library #217744)

  • Purpose

    This CRISPR-based library is designed to target 56 transcription factors in Yarrowia lipolytica, enabling the knockout or modulation of expression levels for these factors. By replacing the native promoters of these transcription factors with alternatives of varying strengths, the library facilitates precise control over their expression in Y. lipolytica. The library can be used for knockout, activation, or inhibition.

  • Vector Backbone

    pCfB3405 (Plasmid #106166) - does not express Cas9

Ordering

Item Catalog # Description Quantity Price (USD)
Pooled Library 217744 TUNEYALI 1 $380 Add to Cart
Available to Academic and Nonprofits Only
  • A Cas9 plasmid is NOT included with this item and will have to be ordered separately. Can be used in conjunction with pCRISPRyl (Addgene #70007), pCAS1yl (Addgene #73226), or any other plasmid expressing Cas9 in Y. lipolytica.

Library Details

  • Species
    Yarrowia lipolytica
  • Genes targeted
    56 transcription factors
  • gRNAs
    1 gRNA per gene

Library Shipping

Each library is delivered in a microcentrifuge tube on blue ice. The tube's contents will not necessarily be frozen. For best results, minimize freeze/thaws.

  • Volume
    ∼20 µL
  • Concentration
    25 ng/µL

Resource Information

Depositor Comments

A cartoon of the TUNEYALI library workflow. The pool of constructs, each containing a gRNA, promoter, ampicillin resistance, and hygromycin selection, are transformed into Y. lipolytica. CRISPR-based High-throughput genome editing tools are used to modulate expression levels of transcription factors (up-regulation or down-regulation) by using Cas9 to cut between the promoter region and the target gene, and then subsequently analyzed using a high-throughput platform.

Figure 1: A CRISPR-Cas9-based method, TUNEYALI, designed for high-throughput gene expression tuning in the widely used industrial yeast Y. lipolytica. The TUNEYALI library facilitates the optimization of Y. lipolytica by targeting 56 transcription factors (TFs) and modulating their expression levels. Using a high-throughput screening platform, strains with optimal performance can be efficiently identified.

How to cite this pooled library ( Back to top )

These pooled libraries were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.

  • For your Materials & Methods section:

    TUNEYALI library was a gift from Irina Borodina (Addgene #217744 ; http://n2t.net/addgene:217744 ; RRID:Addgene_217744)