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Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation
by
Takeichi, Takuya
, Okamoto, Tatsuya
, Miyasaka, Yuki
, Ito, Komei
, McGrath, John A.
, Nishida, Emi
, Lee, John Y. W.
, Murase, Yuya
, Ohno, Tamio
, Okuno, Yusuke
, Yoshikawa, Takenori
, Muro, Yoshinao
, Sugiura, Kazumitsu
, Akiyama, Masashi
, Tanahashi, Kana
in
Age
/ Animal models
/ Animals
/ Autism
/ Autistic Disorder - genetics
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - pathology
/ brain
/ CRISPR
/ Cytokines
/ Disease Models, Animal
/ Down-regulation
/ Female
/ Gene Knock-In Techniques
/ Gene targeting
/ Genomes
/ Hepatitis
/ Hepatitis, Autoimmune - genetics
/ Hepatitis, Autoimmune - pathology
/ Hereditary diseases
/ Humans
/ Hyperactivity
/ Immunology
/ inflammation
/ Janus kinase
/ Janus Kinase 1 - genetics
/ Keratinization
/ Kinases
/ Laboratory animals
/ Leukemia
/ Liver
/ Liver diseases
/ Medical research
/ Mice
/ Missense mutation
/ Monoclonal antibodies
/ Mutation
/ Mutation, Missense
/ NF-κB protein
/ Phenotypes
/ Plasmids
/ Proteins
/ Skin
/ Skin Diseases - genetics
/ Skin Diseases - pathology
/ STAT
/ Young Adult
2022
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Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation
by
Takeichi, Takuya
, Okamoto, Tatsuya
, Miyasaka, Yuki
, Ito, Komei
, McGrath, John A.
, Nishida, Emi
, Lee, John Y. W.
, Murase, Yuya
, Ohno, Tamio
, Okuno, Yusuke
, Yoshikawa, Takenori
, Muro, Yoshinao
, Sugiura, Kazumitsu
, Akiyama, Masashi
, Tanahashi, Kana
in
Age
/ Animal models
/ Animals
/ Autism
/ Autistic Disorder - genetics
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - pathology
/ brain
/ CRISPR
/ Cytokines
/ Disease Models, Animal
/ Down-regulation
/ Female
/ Gene Knock-In Techniques
/ Gene targeting
/ Genomes
/ Hepatitis
/ Hepatitis, Autoimmune - genetics
/ Hepatitis, Autoimmune - pathology
/ Hereditary diseases
/ Humans
/ Hyperactivity
/ Immunology
/ inflammation
/ Janus kinase
/ Janus Kinase 1 - genetics
/ Keratinization
/ Kinases
/ Laboratory animals
/ Leukemia
/ Liver
/ Liver diseases
/ Medical research
/ Mice
/ Missense mutation
/ Monoclonal antibodies
/ Mutation
/ Mutation, Missense
/ NF-κB protein
/ Phenotypes
/ Plasmids
/ Proteins
/ Skin
/ Skin Diseases - genetics
/ Skin Diseases - pathology
/ STAT
/ Young Adult
2022
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Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation
by
Takeichi, Takuya
, Okamoto, Tatsuya
, Miyasaka, Yuki
, Ito, Komei
, McGrath, John A.
, Nishida, Emi
, Lee, John Y. W.
, Murase, Yuya
, Ohno, Tamio
, Okuno, Yusuke
, Yoshikawa, Takenori
, Muro, Yoshinao
, Sugiura, Kazumitsu
, Akiyama, Masashi
, Tanahashi, Kana
in
Age
/ Animal models
/ Animals
/ Autism
/ Autistic Disorder - genetics
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - pathology
/ brain
/ CRISPR
/ Cytokines
/ Disease Models, Animal
/ Down-regulation
/ Female
/ Gene Knock-In Techniques
/ Gene targeting
/ Genomes
/ Hepatitis
/ Hepatitis, Autoimmune - genetics
/ Hepatitis, Autoimmune - pathology
/ Hereditary diseases
/ Humans
/ Hyperactivity
/ Immunology
/ inflammation
/ Janus kinase
/ Janus Kinase 1 - genetics
/ Keratinization
/ Kinases
/ Laboratory animals
/ Leukemia
/ Liver
/ Liver diseases
/ Medical research
/ Mice
/ Missense mutation
/ Monoclonal antibodies
/ Mutation
/ Mutation, Missense
/ NF-κB protein
/ Phenotypes
/ Plasmids
/ Proteins
/ Skin
/ Skin Diseases - genetics
/ Skin Diseases - pathology
/ STAT
/ Young Adult
2022
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Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation
Journal Article
Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation
2022
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Overview
Heterozygous mutations in JAK1 which result in JAK-STAT hyperactivity have been implicated in an autosomal dominant disorder that features multi-organ immune dysregulation. This study identifies another previously unreported heterozygous missense JAK1 mutation, H596D, in an individual with a unique autoinflammatory keratinization disease associated with early-onset liver dysfunction and autism. Using CRISPR-Cas9 gene targeting, we generated mice with an identical Jak1 knock-in missense mutation ( Jak1 H595D/+;I596I/+;Y597Y/+ mice) that recapitulated key aspects of the human phenotype. RNA sequencing of samples isolated from the Jak1 H595D/+;I596I/+;Y597Y/+ mice revealed the upregulation of genes associated with the hyperactivation of tyrosine kinases and NF-κB signaling. Interestingly, there was a strong correlation between genes downregulated in Jak1 H595D/+;I596I/+;Y597Y/+ mice and those downregulated in the brain of model mice with 22q11.2 deletion syndrome that showed cognitive and behavioral deficits, such as autism spectrum disorders. Our findings expand the phenotypic spectrum of JAK1 -associated disease and underscore how JAK1 dysfunction contributes to this autoinflammatory disorder.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
/ Animals
/ Autism
/ Autistic Disorder - genetics
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - pathology
/ brain
/ CRISPR
/ Female
/ Genomes
/ Hepatitis, Autoimmune - genetics
/ Hepatitis, Autoimmune - pathology
/ Humans
/ Kinases
/ Leukemia
/ Liver
/ Mice
/ Mutation
/ Plasmids
/ Proteins
/ Skin
/ STAT
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