<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou W</submitter><funding>NCRR NIH HHS</funding><pagination>e31997</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3278458</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(2)</volume><pubmed_abstract>We have recently developed a so-called genomic engineering approach that allows for directed, efficient and versatile modifications of Drosophila genome by combining the homologous recombination (HR)-based gene targeting with site-specific DNA integration. In genomic engineering and several similar approaches, a "founder" knock-out line must be generated first through HR-based gene targeting, which can still be a potentially time and resource intensive process. To significantly improve the efficiency and success rate of HR-based gene targeting in Drosophila, we have generated a new dual-selection marker termed W::Neo, which is a direct fusion between proteins of eye color marker White (W) and neomycin resistance (Neo). In HR-based gene targeting experiments, mutants carrying W::Neo as the </pubmed_abstract><journal>PloS one</journal><pubmed_title>W::Neo: a novel dual-selection marker for high efficiency gene targeting in Drosophila.</pubmed_title><pmcid>PMC3278458</pmcid><funding_grant_id>R21 RR024869</funding_grant_id><funding_grant_id>R21RR024869</funding_grant_id><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Watson AM</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors></additional><is_claimable>false</is_claimable><name>W::Neo: a novel dual-selection marker for high efficiency gene targeting in Drosophila.</name><description>We have recently developed a so-called genomic engineering approach that allows for directed, efficient and versatile modifications of Drosophila genome by combining the homologous recombination (HR)-based gene targeting with site-specific DNA integration. In genomic engineering and several similar approaches, a "founder" knock-out line must be generated first through HR-based gene targeting, which can still be a potentially time and resource intensive process. To significantly improve the efficiency and success rate of HR-based gene targeting in Drosophila, we have generated a new dual-selection marker termed W::Neo, which is a direct fusion between proteins of eye color marker White (W) and neomycin resistance (Neo). In HR-based gene targeting experiments, mutants carrying W::Neo as the </description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-04-22T07:04:28.19Z</modification><creation>2019-03-26T23:12:37Z</creation></dates><accession>S-EPMC3278458</accession><cross_references><pubmed>22348139</pubmed><doi>10.1371/journal.pone.0031997</doi></cross_references></HashMap>