Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractArea under the blood concentration-time curve (AUC) of ethylbenzene concentration in rats: relationship to inhalation and oral administration route-dose    Next Abstract"Hormonal control of head-wart development in the snail, Euhadra peliomphala" »

Genes Cells


Title:Gene trapping reveals a new transcriptionally active genome element: The chromosome-specific clustered trap region
Author(s):Takeda I; Araki M; Ishiguro KI; Ohga T; Takada K; Yamaguchi Y; Hashimoto K; Kai T; Nakagata N; Imasaka M; Yoshinobu K; Araki K;
Address:"Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan. Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan"
Journal Title:Genes Cells
Year:2021
Volume:20210830
Issue:11
Page Number:874 - 890
DOI: 10.1111/gtc.12890
ISSN/ISBN:1365-2443 (Electronic) 1356-9597 (Linking)
Abstract:"Nearly half of the human genome consists of repetitive sequences such as long interspersed nuclear elements. The relationship between these repeating sequences and diseases has remained unclear. Gene trapping is a useful technique for disrupting a gene and expressing a reporter gene by using the promoter activity of the gene. The analysis of trapped genes revealed a new genome element-the chromosome-specific clustered trap (CSCT) region. For any examined sequence within this region, an equivalent was found using the BLAT of the University of California, Santa Cruz (UCSC) Genome Browser. CSCT13 mapped to chromosome 13 and contained only three genes. To elucidate its in vivo function, the whole CSCT13 region (1.6 Mbp) was deleted using the CRISPR/Cas9 system in mouse embryonic stem cells, and subsequently, a CSCT13 knockout mouse line was established. The rate of homozygotes was significantly lower than expected according to Mendel's laws. In addition, the number of offspring obtained by mating homozygotes was significantly smaller than that obtained by crossing controls. Furthermore, CSCT13 might have an effect on meiotic homologous recombination. This study identifies a transcriptionally active CSCT with an important role in mouse development"
Keywords:"Animals CRISPR-Cas Systems/genetics Chromosomes/genetics Genes, Reporter *Genome Mice *Repetitive Sequences, Nucleic Acid Software gene trap genome editing repetitive sequence segmental duplication;"
Notes:"MedlineTakeda, Iyo Araki, Masatake Ishiguro, Kei-Ichiro Ohga, Toshinori Takada, Kouki Yamaguchi, Yusuke Hashimoto, Koichi Kai, Takuma Nakagata, Naomi Imasaka, Mai Yoshinobu, Kumiko Araki, Kimi eng 16K07093/Ministry of Education, Culture, Sports, Science and Technology/ JP16H06276/Ministry of Education, Culture, Sports, Science and Technology/ JP20300146/Ministry of Education, Culture, Sports, Science and Technology/ JP23300159/Ministry of Education, Culture, Sports, Science and Technology/ JP23310135/Ministry of Education, Culture, Sports, Science and Technology/ JP25640052/Ministry of Education, Culture, Sports, Science and Technology/ England 2021/08/22 Genes Cells. 2021 Nov; 26(11):874-890. doi: 10.1111/gtc.12890. Epub 2021 Aug 30"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-11-2024