Literature DB >> 35656878

Generation of FLAG-tagged Arx knock-in mouse model.

Youngshin Lim1, Il-Taeg Cho1, Jeffrey A Golden1, Ginam Cho1.   

Abstract

The Aristaless-related homeobox (ARX) is a paired-like homeodomain transcription factor playing important roles in brain development. Patients with mutations in ARX have a spectrum of neurodevelopmental disorders such as epilepsy, intellectual disability, and autism spectrum disorder, with or without structural abnormalities of the brain such as lissencephaly (smooth brain), microcephaly (small brain), and/or agenesis of the corpus callosum. Mouse models have provided important clues on the pathophysiologic roles of ARX in these disorders. However, successfully isolating specific in vivo complexes of ARX, with DNA and proteins, has remained as a challenge. To facilitate in vivo detection of ARX complexes, we generated a mouse line containing one epitope of FLAG-tag (1 × FLAG) targeted at the translational start site of the endogenous Arx gene using CRSPR/Cas9 strategy. Homozygous Flag-Arx mice are viable and fertile without gross abnormality, suggesting that the FLAG-tag does not perturb the normal function of ARX. Using a FLAG antibody, we successfully detected ARX with immunofluorescent staining and pulled down ARX in embryonic brain tissues. This Flag-Arx mouse line will be a useful tool to isolate ARX complexes from mouse tissues for many applications.
© 2022 Wiley Periodicals LLC.

Entities:  

Keywords:  ARX; CRSPR/cas9; Flag-Arx knock-in mouse; brain development; detection of FLAG tagged-endogenous protein

Mesh:

Substances:

Year:  2022        PMID: 35656878      PMCID: PMC9333336          DOI: 10.1002/dvg.23479

Source DB:  PubMed          Journal:  Genesis        ISSN: 1526-954X            Impact factor:   2.389


  27 in total

Review 1.  Neurons on the move: migration and lamination of cortical interneurons.

Authors:  Clare Faux; Sonja Rakic; William Andrews; Joanne M Britto
Journal:  Neurosignals       Date:  2012-05-04

2.  Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.

Authors:  Kunio Kitamura; Masako Yanazawa; Noriyuki Sugiyama; Hirohito Miura; Akiko Iizuka-Kogo; Masatomo Kusaka; Kayo Omichi; Rika Suzuki; Yuko Kato-Fukui; Kyoko Kamiirisa; Mina Matsuo; Shin-ichi Kamijo; Megumi Kasahara; Hidefumi Yoshioka; Tsutomu Ogata; Takayuki Fukuda; Ikuko Kondo; Mitsuhiro Kato; William B Dobyns; Minesuke Yokoyama; Ken-ichirou Morohashi
Journal:  Nat Genet       Date:  2002-10-15       Impact factor: 38.330

3.  Epidemiological and clinical studies of West syndrome in Nagasaki Prefecture, Japan.

Authors:  A Matsuo; T Matsuzaka; A Tsuru; H Moriuchi; Y Nakashita; S Tanaka; C Baba; K Tomimasu
Journal:  Brain Dev       Date:  2001-11       Impact factor: 1.961

4.  Immunohistochemical detection of FLAG-tagged endogenous proteins in knock-in mice.

Authors:  Ronald E Ferrando; Kim Newton; Felix Chu; Joshua D Webster; Dorothy M French
Journal:  J Histochem Cytochem       Date:  2015-01-09       Impact factor: 2.479

5.  Mutations in ARX Result in Several Defects Involving GABAergic Neurons.

Authors:  Gaëlle Friocourt; John G Parnavelas
Journal:  Front Cell Neurosci       Date:  2010-03-11       Impact factor: 5.505

6.  Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor.

Authors:  O McKenzie; I Ponte; M Mangelsdorf; M Finnis; G Colasante; C Shoubridge; S Stifani; J Gécz; V Broccoli
Journal:  Neuroscience       Date:  2007-02-27       Impact factor: 3.590

Review 7.  Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development.

Authors:  Chiaki Ohtaka-Maruyama; Haruo Okado
Journal:  Front Neurosci       Date:  2015-12-17       Impact factor: 4.677

8.  ARX regulates cortical intermediate progenitor cell expansion and upper layer neuron formation through repression of Cdkn1c.

Authors:  Gaia Colasante; Jacqueline C Simonet; Raffaele Calogero; Stefania Crispi; Alessandro Sessa; Ginam Cho; Jeffrey A Golden; Vania Broccoli
Journal:  Cereb Cortex       Date:  2013-08-22       Impact factor: 5.357

9.  Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.

Authors:  Mitsuhiro Kato; Soma Das; Kristin Petras; Kunio Kitamura; Ken-Ichirou Morohashi; Diane N Abuelo; Mason Barr; Dominique Bonneau; Angela F Brady; Nancy J Carpenter; Karen L Cipero; Francesco Frisone; Takayuki Fukuda; Renzo Guerrini; Eri Iida; Masayuki Itoh; Amy Feldman Lewanda; Yukiko Nanba; Akira Oka; Virginia K Proud; Pascale Saugier-Veber; Susan L Schelley; Angelo Selicorni; Rachel Shaner; Margherita Silengo; Fiona Stewart; Noriyuki Sugiyama; Jun Toyama; Annick Toutain; Ana Lía Vargas; Masako Yanazawa; Elaine H Zackai; William B Dobyns
Journal:  Hum Mutat       Date:  2004-02       Impact factor: 4.878

Review 10.  The aristaless (Arx) gene: one gene for many "interneuronopathies".

Authors:  Martino Ruggieri; Piero Pavone; Giovanni Scapagnini; Loriana Romeo; Ilaria Lombardo; Giovanni Li Volti; Giovanni Corsello; Lorenzo Pavone
Journal:  Front Biosci (Elite Ed)       Date:  2010-01-01
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