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Gfi1-GCE inducible Cre line for hair cell-specific gene manipulation in mouse inner ear

*Corresponding author for this work
  • University of Rochester
    ,
  • Chinese Academy of Medical Sciences
    ,
  • Hangzhou Normal University
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Tissue-specific inducible Cre recombinase mouse lines allow precise genetic manipulations in spatiotemporal manners and are pivotal for functional studies of genes during development and in adults. Growth factor independence 1 (GFI1) is an essential transcription factor expressed in the hair cells of mouse inner ear and Gfi1 locus serves as an excellent anchor site to drive the expression of inducible Cre recombinase in mouse inner hair cells. In this study, we have generated Gfi1-P2A-GFP-CreERT2 (Gfi1-GCE) knock-in mouse line by in-frame fusion of a self-cleaving GCE to the C-terminus of GFI1. We have shown that as predicted, the expression of GCE and GFI1 was detected specifically in the cytosol and nuclei of hair cells, respectively, of uninduced Gfi1-GCE mice, suggesting the successful cleavage and simultaneous expression of GFI1 and GCE. In addition, the in-frame fusion of the self-cleaving GCE does not interrupt the function of Gfi1 in the inner ear. Administration of tamoxifen leads to nuclear translocation of GCE and results in an efficient activation of tdTomato reporter gene expression specifically in most hair cells throughout development and in adults. Thus, this inducible Gfi1-GCE mouse line is a highly efficient Cre deleter and is suitable for gene manipulation in developing and adult inner ear hair cells.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e23304

Journal (Volume, Issue Number)

Genesis (Volume 57, Issue 9)

Publication milestones

  • Published - 09/01/2019

Publication status

Published - 09/01/2019

ISSN

1526-954X

Publication IDs

  • Scopus: 85065746124
  • PubMed: 31077553
  • ORCID: /0000-0001-6764-1185/work/68887608

Publication metrics

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SciVal
FWCI
0.14
SciVal
Author count
6
SciVal
citations
1
SciVal
Paper percentile
49
Fractional count
2
Fractional count
0.33
Fractional count
4
Fractional count
0.67
Fractional count
2
Fractional count
1
Scopus
citations

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Captures
16
Citation count
8

Funding Details

We thank the members of Gan laboratory for their insightful discussions and University of Rochester Mouse Gene Editing Resource for assisting with the generation of Gfi1-GCE mouse model. This research was supported by Beijing Natural Science Foundation (NO. 7172176) and National key research and development plan of China (NO. 2016YFA0101000, NO. 2016YFA0101002) to H.Y., the National Institute of Health grant (EY026614) to L.G., the Research to Prevent Blindness challenge grant to the Department of Ophthalmology and the P30 center core grant (EY01319F) to the Center for Visual Science at the University of Rochester.
FundersFunding numbers
Ophthalmology Department
-
Challenge Grants from Research to Prevent Blindness
-
FNIH
EY026614
CORE
EY01319F
UR
-
CVS
-
Natural Science Foundation of Beijing Municipality
7172176
National Key Research and Development Program of China Stem Cell and Translational Research
2016YFA0101000, 2016YFA0101002