FLP-mediated removal of extraneous sequences (A) Schematic representation of FLP-mediated removal of extraneous sequences. FLP-mediated removal of extraneous.

Slides:



Advertisements
Similar presentations
Genetic Transformation of Plants: Methods and Approaches to Develop Transgenic plants.
Advertisements

Today: Biotechnology Exam #2 Th 10/23 in class.
A Robust Network of Double-Strand Break Repair Pathways Governs Genome Integrity during C. elegans Development  Daphne B. Pontier, Marcel Tijsterman 
Visualization of trans-Homolog Enhancer-Promoter Interactions at the Abd-B Hox Locus in the Drosophila Embryo  Matthew Ronshaugen, Mike Levine  Developmental.
Recombination based transformation technologies
The Human Genome Project
The Human Genome Project
attP region and attB regions
Role of C-terminal phosphorylation in the subcellular localization of AtPIP2;1 in response to salinity. Role of C-terminal phosphorylation in the subcellular.
Role of C-terminal phosphorylation in the subcellular localization of AtPIP2;1.A, the figure shows typical laser-scanning confocal micrographs of the fluorescence.
Workflow of one-step integration into any potential chromosome location. Workflow of one-step integration into any potential chromosome location. (A) After.
Volume 10, Issue 4, Pages (October 2004)
A subset of multiple myeloma harboring the t(4;14)(p16;q32) translocation lacks FGFR3 expression but maintains anIGH/MMSET fusion transcript by Madhumita.
Rationale for generation of reporter fusions by Red-mediated recombination. Rationale for generation of reporter fusions by Red-mediated recombination.
Zebrafish as a Model System to Study Skin Biology and Pathology
The let-7 microRNA Directs Vulval Development through a Single Target
Characterisation of proviral integrations in corrected stem cells Visualisation of COL7A1 sequence by FISH analysis in corrected stem cells at passage.
Fig. 4. Liver HBV mRNA paired-end sequencing reads in HBeAg-positive and HBeAg-negative chimpanzees. Liver HBV mRNA paired-end sequencing reads in HBeAg-positive.
cpDNAs with large deletions accumulate in cptk1 mutants.
Highly efficient lentiviral-mediated human cytokine transgenesis on the NOD/scid background by Isabel Punzon, Luis M. Criado, Alfredo Serrano, Fernando.
Volume 28, Issue 1, Pages (January 2014)
Direct fusion lines allow fluorescent visualization of plasmatocyte nuclei, the cytoplasm, or the cytoskeleton in embryos from stage (St) 8 onwards. Direct.
Lineage Tracing Cell Volume 148, Issue 1, Pages (January 2012)
Transgenic Mouse Technology in Skin Biology: Generation of Knockin Mice  Frederik Tellkamp, Farida Benhadou, Jeroen Bremer, Maria Gnarra, Jana Knüver,
lgc-35 (L324S) CRISPR-Cas9-RNP genotyping and Mendelian segregation.
Zebrafish: A Model System to Study Heritable Skin Diseases
Pnut is phosphorylated during early Drosophila embryogenesis.
Schematic representation of the lbk gene, positions of gRNAs, and knock-in cassette. Schematic representation of the lbk gene, positions of gRNAs, and.
Volume 17, Issue 2, Pages (August 2015)
The let-7 microRNA Directs Vulval Development through a Single Target
Volume 10, Issue 7, Pages (July 2017)
Andriana G Kotini, Michel Sadelain, Eirini P Papapetrou 
Subcellular localization of FZR-1 during the first cell cycle.
Identification of translocations (via homeologous exchanges) in four G3 plants using BAC-FISH. Identification of translocations (via homeologous exchanges)
Immunofluorescent analysis of early Drosophila embryos.
Targeted Myostatin Gene Editing in Multiple Mammalian Species Directed by a Single Pair of TALE Nucleases  Li Xu, Piming Zhao, Andrew Mariano, Renzhi.
Volume 17, Issue 6, Pages (November 2016)
A. A. The two independent mutations identified in the structural gene of pqn-82 are shown above the gene. The genomic coordinates for the altered base.
Viral genetic targeting of hilar mossy cells for rabies-based mapping of circuit connections in vivo. Viral genetic targeting of hilar mossy cells for.
QRT-PCR analysis of the role of MDL-1 in expression of infection-regulated genes. qRT-PCR analysis was performed on infection-regulated genes that have.
Mutagenesis through Cas9/sgRNA-induced HDR
Volume 25, Issue 2, Pages (February 2017)
Transcript length distribution resulting from different assemblies of the embryo samples across the three technologies (HiSeq, MiSeq, and PacBio). Transcript.
Mapping rates of different transcript sets to the P
Calcineurin inhibition impairs neutrophil recruitment in a zebrafish model of invasive aspergillosisAt 2 days post‐fertilization (dpf), Lyz:dsRed or mpx:GFP.
T7 transcripts increase relative to E. coli transcripts over time.
Volume 7, Issue 12, Pages (December 2014)
Targeted disruption of the RapGEF2 gene.
Generation of iTS cells via ES cells carrying an inducible Cdx2 transgene. Generation of iTS cells via ES cells carrying an inducible Cdx2 transgene. (A)
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
Fig. 4. Mutations induced by TALENs are heritable through the germline
The initial targeting of Sec61b mRNA to the ER is partially dependent on ribosomes and translation. The initial targeting of Sec61b mRNA to the ER is partially.
Fig. 2. Validating the efficiency of smc3 MOs
P53 is responsible for the induction of apoptosis, developmental malformations and mortality of G1 and G2tert mutant zebrafish. p53 is responsible for.
Cdx2 and Oct4 bind to Xist and Xite in vivo.
Allele size distribution and frequency observed at 17 microsatellite loci in A. gambiae M (M, shaded bars), A. gambiae S (S, solid bars), and A. arabiensis.
The FRAP mobility of EGFP-UAP56, but not its K95N mutant, is ATP-dependent. The FRAP mobility of EGFP-UAP56, but not its K95N mutant, is ATP-dependent.
Schematic design of the SSM
Manhattan plots for GWAS of LD50, µg/ml survival, 0
Genomic structure of LTBP-4 around the 3rd 8-Cys repeat.
Chd1 expression and CHD1 localization during mouse preimplantation development. Chd1 expression and CHD1 localization during mouse preimplantation development.
A two-step method to flexibly engineer the fly genome.
Methods used to generate genetically modified pigs.
Sequence variation of 16S rRNA gene primer-binding sites.
Generation of an inducible tissue-specific Atoh1 transgenic mouse line
IEG promoter-driven transgenic reporter system in the cricket brain.
Loss of CTCF causes p53-dependent transcriptional activation of Puma.
Purification scheme. Purification scheme. (A) Line drawing of CelTag fragment from CelTag plasmid. PCR (polymerase chain reaction) of fragment was performed.
Phylogeny and expression landscape of Wolbachia in D. melanogaster.
Volume 150, Issue 1, Pages (July 2012)
Presentation transcript:

FLP-mediated removal of extraneous sequences (A) Schematic representation of FLP-mediated removal of extraneous sequences. FLP-mediated removal of extraneous sequences (A) Schematic representation of FLP-mediated removal of extraneous sequences. (B) Schematic representation of the attP-landing site in chromosome 13 before and after phiC31 integrase-mediated integration of the Pzhsp70-mCherry-pA as well as subsequent FLP-mediated removal of extraneous sequences. (C) Typical observations of mCherry and EGFP fluorescence emitted by transgenic G0 fish carrying the Pzhsp70-mCherry-pA at an attP-landing site before (-) or after (+) FLP-mediated removal of extraneous sequences. Scale bar: 1 mm. (D) Transgenic fish harboring the Pzhsp70-mCherry-pA at the attP-landing site were incrossed, and one-cell-stage embryos were microinjected with 100 ng/µl of FLP mRNA. The 45 surviving embryos were observed at 5 dpf for mCherry and EGFP fluorescence after heat shock. (E) Survival rates at 5 dpf of embryos microinjected with 100 ng/μl of FLP mRNA. (F) Genomic PCR using the three primer pairs of three types of embryos with the attP-landing site structure shown in (B). Tokiro Ishikawa et al. G3 2018;8:2585-2593 ©2018 by Genetics Society of America