抄録
Luo et al. report variable rates of germline recombination in commonly used mouse Cre driver lines, influenced by sex of Cre-carrying parents and target loci. Guidelines are provided to optimize cell-type-specific recombination in genetically targeted organisms expressing site-specific recombinases.
本文言語 | English |
---|---|
ページ(範囲) | 37-65.e5 |
ジャーナル | Neuron |
巻 | 106 |
号 | 1 |
DOI | |
出版ステータス | Published - 2020 4月 8 |
ASJC Scopus subject areas
- 神経科学(全般)
フィンガープリント
「Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。引用スタイル
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In: Neuron, Vol. 106, No. 1, 08.04.2020, p. 37-65.e5.
研究成果: Article › 査読
}
TY - JOUR
T1 - Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines
T2 - Prevalence of Germline Recombination and Influencing Factors
AU - Luo, Lin
AU - Ambrozkiewicz, Mateusz C.
AU - Benseler, Fritz
AU - Chen, Cui
AU - Dumontier, Emilie
AU - Falkner, Susanne
AU - Furlanis, Elisabetta
AU - Gomez, Andrea M.
AU - Hoshina, Naosuke
AU - Huang, Wei Hsiang
AU - Hutchison, Mary Anne
AU - Itoh-Maruoka, Yu
AU - Lavery, Laura A.
AU - Li, Wei
AU - Maruo, Tomohiko
AU - Motohashi, Junko
AU - Pai, Emily Ling Lin
AU - Pelkey, Kenneth A.
AU - Pereira, Ariane
AU - Philips, Thomas
AU - Sinclair, Jennifer L.
AU - Stogsdill, Jeff A.
AU - Traunmüller, Lisa
AU - Wang, Jiexin
AU - Wortel, Joke
AU - You, Wenjia
AU - Abumaria, Nashat
AU - Beier, Kevin T.
AU - Brose, Nils
AU - Burgess, Harold A.
AU - Cepko, Constance L.
AU - Cloutier, Jean François
AU - Eroglu, Cagla
AU - Goebbels, Sandra
AU - Kaeser, Pascal S.
AU - Kay, Jeremy N.
AU - Lu, Wei
AU - Luo, Liqun
AU - Mandai, Kenji
AU - McBain, Chris J.
AU - Nave, Klaus Armin
AU - Prado, Marco A.M.
AU - Prado, Vania F.
AU - Rothstein, Jeffrey
AU - Rubenstein, John L.R.
AU - Saher, Gesine
AU - Sakimura, Kenji
AU - Sanes, Joshua R.
AU - Scheiffele, Peter
AU - Takai, Yoshimi
AU - Umemori, Hisashi
AU - Verhage, Matthijs
AU - Yuzaki, Michisuke
AU - Zoghbi, Huda Yahya
AU - Kawabe, Hiroshi
AU - Craig, Ann Marie
N1 - Funding Information: We thank Dr. Cynthia Smith from the Jackson Laboratory for her open acceptance of our data on the MGI database. We thank Dr. Timothy Murphy for his kind gift of the Ai32 mouse line. We thank Drs. Elizabeth M. Simpson, Sören Lukassen, and the University of British Columbia Dynamic Brain Circuits Cluster for discussion. Work by Lin Luo and A.M.C. was supported by Canadian Institutes of Health Research (FDN-143206) and Simons Foundation Autism Research Initiative (SFARI 608066). Work by M.C.A. and H.K. was supported by German Research Foundation (SPP1365/KA3423/1-1 and KA3423/3-1) and Japan Society for the Promotion of Science (JSPS) KAKENHI grant number 15K21769. Work by N.B. and F.B. was supported by European Research Council (ERC) Advanced Grant SYNPRIME and the German Research Foundation SFB 1286/A9 awards to N.B. Work by C.C. W. Li, and N.A. was supported by the Natural Science Foundation of China grant (81573408), Fudan University-Shanghai Institute of Materia Medica Chinese Academy of Science joint grant (FU-SIMM20174015), and the Shanghai Municipal Science and Technology Major Project (No. 2018SHZDZX01). Work by J.L.S. and H.A.B. was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development. Work by K.T.B. was supported by National Institutes of Health (NIH) grant F32 DA038913 and NIH grant K99/R00 DA041445. Work by W.Y. and C.C. was supported by a Howard Hughes Medical Institute (HHMI) salary awarded to C.C. Work by E.D. and J.-F.C. was supported by the Canadian Institutes of Health Research and the Natural Sciences and Engineering Research Council of Canada (NSERC). Work by J.A.S. and C.E. was supported by NIH grants RO1DA031833 and F31NS092419. Work by J. Wang and P.S.K. was supported by NIH grants R01NS083898, R01NS103484, and R01MH113349. Work by A.P. and J.N.K. was supported by NIH grants EY024694 to J.N.K. and EY5722 to Duke University. Work by M.A.H. and W. Lu was supported by National Institute of Neurological Disorders and Stroke (NINDS) and NIH Intramural Research Program. Work by W.-H.H. and Liqun Luo was supported by HHMI, SFARI Research Award 345098, and NIH grant R01NS050580 to Liqun Luo and NIH grant 5K99HD092545-02 to W.-H.H. Work by T.M. and K.M. was supported by Japan's Ministry of Education, Culture, Sports, Science and Technology KAKENHI grant 16H06463 and JPSP KAKENHI grant 18K06503. Work by K.A.P. and C.J.M. was supported by a Eunice Kennedy Shriver National Institute of Child Health and Human Development Intramural Award. Work by S.G. G.S. and K.-A.N. was supported by ERC Advanced Grants AxoGLIA and MyeliNANO, the German Research Foundation (SPP1757), and the Max Planck Society. Work by M.A.M.P. and V.F.P. was supported by Canadian Institute of Health Research grants MOP136930, MOP89919, PJT 162431, and PJT 159781 and NSERC grant 06577-2018 RGPIN. Work by E.L.-L.P. and J.L.R.R. was supported by NIH NINDS grant R01 NS099099, National Institute of Mental Health (NIMH) grant R01 MH081880, and NIMH grant R01 MH049428. Work by J.R.S. was supported by NIH R37NS029169. Work by S.F. E.F. A.M.G. L.T. and P.S. was supported by ERC Advanced Grant SPLICECODE; Swiss National Science Foundation to P.S. and European Molecular Biology Organization EMBO ALTF-70-2015 and aALTF-760-2016 to A.M.G. Work by Y.T. was supported by JPSP KAKENHI grant 26251013. Work by H.U. was supported by NIH R01DA042744, R01MH111647, R01NS092578, and SFARI grants. Work by J. Wortel and M.V. was supported by an ERC Advanced Grant (322966) of the European Union. Work by J.M. and M.Y. was supported by Japan Science and Technology Agency (JPMJCR1854) and KAKENHI (16H06461 and 15H05772). Work by L.A.L. and H.Y.Z. was supported by NIH/NINDS grant 5R01NS057819-13 as well as HHMI to H.Y.Z. Lin Luo, H.K. and A.M.C. conceived the project. All authors contributed unpublished data to Tables 1 or 2. Lin Luo and A.M.C. generated the figures, collated and analyzed the data, and wrote the manuscript with input from all authors. The authors declare no competing interests. Funding Information: We thank Dr. Cynthia Smith from the Jackson Laboratory for her open acceptance of our data on the MGI database. We thank Dr. Timothy Murphy for his kind gift of the Ai32 mouse line. We thank Drs. Elizabeth M. Simpson, Sören Lukassen, and the University of British Columbia Dynamic Brain Circuits Cluster for discussion. Work by Lin Luo and A.M.C. was supported by Canadian Institutes of Health Research ( FDN-143206 ) and Simons Foundation Autism Research Initiative ( SFARI 608066 ). Work by M.C.A. and H.K. was supported by German Research Foundation ( SPP1365/KA3423/1-1 and KA3423/3-1 ) and Japan Society for the Promotion of Science (JSPS) KAKENHI grant number 15K21769 . Work by N.B. and F.B. was supported by European Research Council (ERC) Advanced Grant SYNPRIME and the German Research Foundation SFB 1286/A9 awards to N.B. Work by C.C., W. Li, and N.A. was supported by the Natural Science Foundation of China grant ( 81573408 ), Fudan University-Shanghai Institute of Materia Medica Chinese Academy of Science joint grant ( FU-SIMM20174015 ), and the Shanghai Municipal Science and Technology Major Project (No. 2018SHZDZX01 ). Work by J.L.S. and H.A.B. was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development . Work by K.T.B. was supported by National Institutes of Health (NIH) grant F32 DA038913 and NIH grant K99/R00 DA041445 . Work by W.Y. and C.C. was supported by a Howard Hughes Medical Institute (HHMI) salary awarded to C.C. Work by E.D. and J.-F.C. was supported by the Canadian Institutes of Health Research and the Natural Sciences and Engineering Research Council of Canada (NSERC) . Work by J.A.S. and C.E. was supported by NIH grants RO1DA031833 and F31NS092419 . Work by J. Wang and P.S.K. was supported by NIH grants R01NS083898 , R01NS103484 , and R01MH113349 . Work by A.P. and J.N.K. was supported by NIH grants EY024694 to J.N.K. and EY5722 to Duke University. Work by M.A.H. and W. Lu was supported by National Institute of Neurological Disorders and Stroke (NINDS) and NIH Intramural Research Program . Work by W.-H.H. and Liqun Luo was supported by HHMI , SFARI Research Award 345098, and NIH grant R01NS050580 to Liqun Luo and NIH grant 5K99HD092545-02 to W.-H.H. Work by T.M. and K.M. was supported by Japan's Ministry of Education, Culture, Sports, Science and Technology KAKENHI grant 16H06463 and JPSP KAKENHI grant 18K06503 . Work by K.A.P. and C.J.M. was supported by a Eunice Kennedy Shriver National Institute of Child Health and Human Development Intramural Award . Work by S.G., G.S., and K.-A.N. was supported by ERC Advanced Grants AxoGLIA and MyeliNANO , the German Research Foundation ( SPP1757 ), and the Max Planck Society . Work by M.A.M.P. and V.F.P. was supported by Canadian Institute of Health Research grants MOP136930 , MOP89919 , PJT 162431 , and PJT 159781 and NSERC grant 06577-2018 RGPIN . Work by E.L.-L.P. and J.L.R.R. was supported by NIH NINDS grant R01 NS099099 , National Institute of Mental Health (NIMH) grant R01 MH081880 , and NIMH grant R01 MH049428 . Work by J.R.S. was supported by NIH R37NS029169 . Work by S.F., E.F., A.M.G., L.T., and P.S. was supported by ERC Advanced Grant SPLICECODE; Swiss National Science Foundation to P.S. and European Molecular Biology Organization EMBO ALTF-70-2015 and aALTF-760-2016 to A.M.G. Work by Y.T. was supported by JPSP KAKENHI grant 26251013 . Work by H.U. was supported by NIH R01DA042744 , R01MH111647 , R01NS092578 , and SFARI grants. Work by J. Wortel and M.V. was supported by an ERC Advanced Grant ( 322966 ) of the European Union. Work by J.M. and M.Y. was supported by Japan Science and Technology Agency ( JPMJCR1854 ) and KAKENHI ( 16H06461 and 15H05772 ). Work by L.A.L. and H.Y.Z. was supported by NIH/NINDS grant 5R01NS057819-13 as well as HHMI to H.Y.Z. Publisher Copyright: © 2020 Elsevier Inc.
PY - 2020/4/8
Y1 - 2020/4/8
N2 - Luo et al. report variable rates of germline recombination in commonly used mouse Cre driver lines, influenced by sex of Cre-carrying parents and target loci. Guidelines are provided to optimize cell-type-specific recombination in genetically targeted organisms expressing site-specific recombinases.
AB - Luo et al. report variable rates of germline recombination in commonly used mouse Cre driver lines, influenced by sex of Cre-carrying parents and target loci. Guidelines are provided to optimize cell-type-specific recombination in genetically targeted organisms expressing site-specific recombinases.
KW - Cre-lox
KW - conditional gene targeting
KW - conditional knockin
KW - conditional knockout
KW - conditional reporter
KW - germline recombination
KW - molecular genetics
KW - mosaic recombination
KW - parental sex bias
KW - site-specific recombinase
UR - http://www.scopus.com/inward/record.url?scp=85082824559&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85082824559&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2020.01.008
DO - 10.1016/j.neuron.2020.01.008
M3 - Article
C2 - 32027825
AN - SCOPUS:85082824559
SN - 0896-6273
VL - 106
SP - 37-65.e5
JO - Neuron
JF - Neuron
IS - 1
ER -