Proteins with clusters of CH zinc finger domains (CH-proteins) constitute the most abundant class of transcription factors in higher eukaryotes. N-terminal ZAD (zinc finger-associated domain) dimerization domain has been identified in a large group of CH-proteins mostly in insects. The piragua gene encodes one of these proteins, Fu2. We have generated CRISPR/Cas9-mediated deletion of the piragua gene that has no phenotype. We have used φC31-mediated attP/attB recombination to generate a transgenic line expressing Fu2 protein fused with HA epitope. This line will be useful for analysis of DNA binding profile and functions of Fu2 protein.
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http://dx.doi.org/10.1134/S0012496621060089 | DOI Listing |
Dokl Biol Sci
November 2021
Institute of Gene Biology, Russian Academy of Sciences, 119334, Moscow, Russia.
Proteins with clusters of CH zinc finger domains (CH-proteins) constitute the most abundant class of transcription factors in higher eukaryotes. N-terminal ZAD (zinc finger-associated domain) dimerization domain has been identified in a large group of CH-proteins mostly in insects. The piragua gene encodes one of these proteins, Fu2.
View Article and Find Full Text PDFPurpose: Brain tumors have become the leading cause of cancer-related mortality in young patients. Novel effective therapies on the basis of the unique biology of each tumor are urgently needed. The goal of this study was to evaluate the feasibility, utility, and clinical impact of integrative clinical sequencing and genetic counseling in children and young adults with high-risk brain tumors.
View Article and Find Full Text PDFMech Dev
April 2017
Departamento de Neurobiología del Desarrollo y Neurofisiología, Instituto de Neurobiología, UNAM, Campus UNAM Juriquilla, Boulevard Juriquilla 3001, Querétaro, Querétaro c.p. 76230, Mexico. Electronic address:
We isolated and characterized embryonic lethal mutations in piragua (prg). The prg locus encodes a protein with an amino terminus Zinc Finger-Associated-Domain (ZAD) and nine CH zinc fingers (ZF). prg mRNA and protein expression during embryogenesis is dynamic with widespread maternal contribution, and subsequent expression in epithelial precursors.
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