FlpStop, a tool for conditional gene control in Drosophila

被引:42
作者
Fisher, Yvette E. [2 ]
Yang, Heien H. [2 ]
Isaacman-Beck, Jesse [1 ]
Xie, Marjorie [1 ]
Gohl, Daryl M. [3 ]
Clandinin, Thomas R. [1 ]
机构
[1] Stanford Univ, Dept Neurobiol, Stanford, CA 94305 USA
[2] Harvard Med Sch, Dept Neurobiol, Boston, MA USA
[3] Univ Minnesota, Genom Ctr, Minneapolis, MN 55455 USA
来源
ELIFE | 2017年 / 6卷
基金
美国国家科学基金会;
关键词
VESICULAR GLUTAMATE TRANSPORTER; SYNAPTIC CALCIUM-CHANNEL; DOUBLE-STRANDED-RNA; GAIN-CONTROL; FLUORESCENT PROTEINS; COURTSHIP BEHAVIOR; MOTION DETECTION; VISUAL-SYSTEM; ANTENNAL LOBE; MELANOGASTER;
D O I
10.7554/eLife.22279
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Manipulating gene function cell type-specifically is a common experimental goal in Drosophila research and has been central to studies of neural development, circuit computation, and behavior. However, current cell type-specific gene disruption techniques in flies often reduce gene activity incompletely or rely on cell division. Here we describe FlpStop, a generalizable tool for conditional gene disruption and rescue in post-mitotic cells. In proof-of-principle experiments, we manipulated apterous, a regulator of wing development. Next, we produced conditional null alleles of Glutamic acid decarboxylase 1 (Gad1) and Resistant to dieldrin (Rdl), genes vital for GABAergic neurotransmission, as well as cacophony (cac) and paralytic (pare), voltage-gated ion channels central to neuronal excitability. To demonstrate the utility of this approach, we manipulated cac in a specific visual interneuron type and discovered differential regulation of calcium signals across subcellular compartments. Thus, FlpStop will facilitate investigations into the interactions between genes, circuits, and computation.
引用
收藏
页数:33
相关论文
共 90 条
  • [1] Synaptic computation
    Abbott, LF
    Regehr, WG
    [J]. NATURE, 2004, 431 (7010) : 796 - 803
  • [2] Functional Specialization of Neural Input Elements to the Drosophila ON Motion Detector
    Ammer, Georg
    Leonhardt, Aljoscha
    Bahl, Armin
    Dickson, Barry J.
    Borst, Alexander
    [J]. CURRENT BIOLOGY, 2015, 25 (17) : 2247 - 2253
  • [3] Highly Efficient Targeted Mutagenesis of Drosophila with the CRISPR/Cas9 System
    Bassett, Andrew R.
    Tibbit, Charlotte
    Ponting, Chris P.
    Liu, Ji-Long
    [J]. CELL REPORTS, 2013, 4 (01): : 220 - 228
  • [4] Processing properties of ON and OFF pathways for Drosophila motion detection
    Behnia, Rudy
    Clark, Damon A.
    Carter, Adam G.
    Clandinin, Thomas R.
    Desplan, Claude
    [J]. NATURE, 2014, 512 (7515) : 427 - U443
  • [5] TIMELINE 100 years of Drosophila research and its impact on vertebrate neuroscience: a history lesson for the future
    Bellen, Hugo J.
    Tong, Chao
    Tsuda, Hiroshi
    [J]. NATURE REVIEWS NEUROSCIENCE, 2010, 11 (07) : 514 - +
  • [6] A Hierarchy of Cell Intrinsic and Target-Derived Homeostatic Signaling
    Bergquist, Sharon
    Dickman, Dion K.
    Davis, Graeme W.
    [J]. NEURON, 2010, 66 (02) : 220 - 234
  • [7] Establishment of a Developmental Compartment Requires Interactions between Three Synergistic Cis-regulatory Modules
    Bieli, Dimitri
    Kanca, Oguz
    Requena, David
    Hamaratoglu, Fisun
    Gohl, Daryl
    Schedl, Paul
    Affolter, Markus
    Slattery, Matthew
    Mueller, Martin
    Estella, Carlos
    [J]. PLOS GENETICS, 2015, 11 (10):
  • [8] The Drosophila melanogaster Mutants apblot and apXasta Affect an Essential apterous Wing Enhancer
    Bieli, Dimitri
    Kanca, Oguz
    Gohl, Daryl
    Denes, Alexandru
    Schedl, Paul
    Affolter, Markus
    Mueller, Martin
    [J]. G3-GENES GENOMES GENETICS, 2015, 5 (06): : 1129 - 1143
  • [9] BRAND AH, 1993, DEVELOPMENT, V118, P401
  • [10] SHAL, SHAB, AND SHAW - 3 GENES ENCODING POTASSIUM CHANNELS IN DROSOPHILA
    BUTLER, A
    WEI, A
    SALKOFF, L
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (08) : 2173 - 2174