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1.
J Vis Exp ; (124)2017 06 16.
Article in English | MEDLINE | ID: mdl-28654078

ABSTRACT

The CRISPR/Cas9 genome engineering system has revolutionized biology by allowing for precise genome editing with little effort. Guided by a single guide RNA (sgRNA) that confers specificity, the Cas9 protein cleaves both DNA strands at the targeted locus. The DNA break can trigger either non-homologous end joining (NHEJ) or homology directed repair (HDR). NHEJ can introduce small deletions or insertions which lead to frame-shift mutations, while HDR allows for larger and more precise perturbations. Here, we present protocols for generating knockout cell lines by coupling established CRISPR/Cas9 methods with two options for downstream selection/screening. The NHEJ approach uses a single sgRNA cut site and selection-independent screening, where protein production is assessed by dot immunoblot in a high-throughput manner. The HDR approach uses two sgRNA cut sites that span the gene of interest. Together with a provided HDR template, this method can achieve deletion of tens of kb, aided by the inserted selectable resistance marker. The appropriate applications and advantages of each method are discussed.


Subject(s)
CRISPR-Cas Systems/genetics , Clustered Regularly Interspaced Short Palindromic Repeats/genetics , Gene Knockout Techniques/methods , Animals , Cell Culture Techniques , Cell Line , Cinnamates/pharmacology , DNA End-Joining Repair/genetics , Genetic Engineering , Humans , Hygromycin B/analogs & derivatives , Hygromycin B/pharmacology , Neomycin/pharmacology , RNA, Guide, Kinetoplastida/genetics , Transfection
2.
Toxicol In Vitro ; 32: 220-31, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26689327

ABSTRACT

We tested the toxicity of thirdhand smoke (THS) using two controlled laboratory exposure scenarios and low levels of THS. One exposure modeled THS in a car parked outdoors, while the second modeled THS in a room without sunlight. The fabrics were exposed to cigarette smoke and then extracted in culture medium. Concentrations of nicotine, nicotine related alkaloids, and tobacco specific nitrosamines (TSNAs) were determined in fresh and aged extracts. The concentration of TSNAs increased with aging in the indoor experiment. THS extracts were used for cytotoxicity testing using mouse neural stem cells (mNSC), human dermal fibroblasts (hDF) and human palatal mesenchyme cells (hPM). Extracts from the car experiment inhibited mNSC proliferation in a live cell imaging assay and induced single strand DNA breaks in mNSC and hDF. In the indoor experiment, THS extracts made with medium containing serum proteins were significantly more toxic than extracts made with basal medium, and mNSC and hPM were more sensitive than hDF. These data indicate that: (1) aging of THS chemical differs on different fabrics and differs with and without sunlight; (2) very few cigarettes are sufficient to produce a toxic THS residue; and (3) protein enhances the efficiency of extraction of cytotoxic chemicals.


Subject(s)
Air Pollutants/toxicity , Air Pollution, Indoor/adverse effects , Textiles , Tobacco Smoke Pollution/adverse effects , Air Pollutants/radiation effects , Alkaloids/analysis , Animals , Automobiles , Cells, Cultured , DNA Damage , Female , Fibroblasts/drug effects , Humans , Mesenchymal Stem Cells/drug effects , Mice , Middle Aged , Neural Stem Cells/drug effects , Nitrosamines/analysis , Sunlight , Textiles/analysis
3.
PLoS One ; 9(2): e88847, 2014.
Article in English | MEDLINE | ID: mdl-24551179

ABSTRACT

The specification of primordial germ cells (PGCs) and subsequent maintenance of germ-line identity in Drosophila embryos has long been thought to occur solely under the control of cell-autonomous factors deposited in the posterior pole plasm during oogenesis. However, here we document a novel role for somatic BMP signaling in the maintenance of PGC fate during the period leading up to embryonic gonad coalescence. We find that PGCs fail to maintain their germline identity when BMP signaling is compromised. They initiate but are unable to properly assemble the germline stem cell-specific organelle, the spectrosome, and they lose expression of the germline-specific gene Vasa. BMP signaling must, however, be finely tuned as there are deleterious consequences to PGCs when the pathway is excessively active. We show that one mechanism used to calibrate the effects of BMP signals is dependent on the Ubc9 homolog Lesswright (Lwr).


Subject(s)
Bone Morphogenetic Proteins/metabolism , Drosophila melanogaster/cytology , Drosophila melanogaster/embryology , Embryo, Nonmammalian/cytology , Germ Cells/cytology , Germ Cells/metabolism , Signal Transduction , Animals , Autocrine Communication , Cell Nucleus/metabolism , Down-Regulation , Drosophila Proteins/metabolism , Embryo, Nonmammalian/metabolism , Embryonic Development , Phosphorylation
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