Generation and analysis of an improved Foxg1-IRES-Cre driver mouse line
Foxg1 expression is highly restricted to the telencephalon and other head structures in the early embryo. This expression pattern has been exploited to generate conditional knockout mice, based on a widely used Foxg1-Cre knock-in line (Foxg1tm1(cre)Skm), in which the Foxg1 coding region was replaced...
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Published in: | Developmental biology Vol. 412; no. 1; pp. 139 - 147 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Elsevier Inc
01-04-2016
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Subjects: | |
Online Access: | Get full text |
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Summary: | Foxg1 expression is highly restricted to the telencephalon and other head structures in the early embryo. This expression pattern has been exploited to generate conditional knockout mice, based on a widely used Foxg1-Cre knock-in line (Foxg1tm1(cre)Skm), in which the Foxg1 coding region was replaced by the Cre gene. The utility of this line, however, is severely hampered for two reasons: (1) Foxg1-Cre mice display ectopic and unpredictable Cre activity, and (2) Foxg1 haploinsufficiency can produce neurodevelopmental phenotypes. To overcome these issues, we have generated a new Foxg1-IRES-Cre knock-in mouse line, in which an IRES-Cre cassette was inserted in the 3′UTR of Foxg1 locus, thus preserving the endogenous Foxg1 coding region and un-translated gene regulatory sequences in the 3′UTR, including recently discovered microRNA target sites. We further demonstrate that the new Foxg1-IRES-Cre line displays consistent Cre activity patterns that recapitulated the endogenous Foxg1 expression at embryonic and postnatal stages without causing defects in cortical development. We conclude that the new Foxg1-IRES-Cre mouse line is a unique and advanced tool for studying genes involved in the development of the telencephalon and other Foxg1-expressing regions starting from early embryonic stages.
•Generation of an improved Foxg1-IRES-Cre driver mouse line.•Cre activity in this line recapitulates the endogenous Foxg1 expression pattern.•This line lacks neurodevelopmental defects associated with Foxg1 haploinsufficiency.•This driver will facilitate the genetic dissection of forebrain development/function. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan. Present address: MRC Centre for Developmental Neurobiology, Kings College London, New Hunts House, Guys Campus, London SE1 1UL, UK. |
ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/j.ydbio.2016.02.011 |