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1.
Tokai J Exp Clin Med ; 49(3): 133-136, 2024 Sep 20.
Artigo em Inglês | MEDLINE | ID: mdl-39182182

RESUMO

Abnormalities in MYO5B, which encodes an unconventional myosin Vb, not only cause microvillus inclusion disease but also cholestatic liver disease, including benign recurrent intrahepatic cholestasis (BRIC). However, MYO5B-related cholestasis has not yet been reported in Japan. In this study, we present the case of a female patient in her thirties, who had developed jaundice, without diarrhea, in the first year after birth. The jaundice spontaneously subsided and occasionally recurred. Whole-exome sequencing identified two pathogenic variants in MYO5B: a nonsense mutation (c. G1124A: p. W375X) and a missense mutation (c.C2470T: p.R824C). Therefore, the patient was diagnosed with MYO5B-associated BRIC. This is the first reported case of cholestasis with a defined MYO5B defect in Japan.


Assuntos
Colestase Intra-Hepática , Códon sem Sentido , Sequenciamento do Exoma , Mutação de Sentido Incorreto , Miosina Tipo V , Recidiva , Humanos , Miosina Tipo V/genética , Miosina Tipo V/deficiência , Feminino , Colestase Intra-Hepática/genética , Colestase Intra-Hepática/etiologia , Adulto , Cadeias Pesadas de Miosina/genética , Japão , Icterícia/etiologia
2.
Genome Biol ; 23(1): 228, 2022 10 25.
Artigo em Inglês | MEDLINE | ID: mdl-36284311

RESUMO

CRISPR tools can generate knockout and knock-in animal models easily, but the models can contain off-target genomic lesions or random insertions of donor DNAs. Simpler methods to identify off-target lesions and random insertions, using tail or earpiece DNA, are unavailable. We develop CRISPR-KRISPR (CRISPR-Knock-ins and Random Inserts Searching PRotocol), a method to identify both off-target lesions and random insertions. CRISPR-KRISPR uses as little as 3.4 µg of genomic DNA; thus, it can be easily incorporated as an additional step to genotype founder animals for further breeding.


Assuntos
Sistemas CRISPR-Cas , Repetições Palindrômicas Curtas Agrupadas e Regularmente Espaçadas , Camundongos , Animais , Técnicas de Introdução de Genes , DNA/genética , Genoma , Edição de Genes/métodos
4.
Biology (Basel) ; 11(4)2022 04 13.
Artigo em Inglês | MEDLINE | ID: mdl-35453788

RESUMO

This study aimed to clarify whether genetic mutations participate in renal cell carcinoma (RCC) metastasis to the adrenal gland (AG). Our study analyzed whole mitochondrial gene and ribonucleic acid sequencing (RNA-seq) data from a male patient in his 60s with metastatic RCC. We confirmed common mutation sites in the mitochondrial gene and carried out Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis using RNA-seq data for RCC and adrenal carcinoma. Furthermore, we confirmed the common mutation sites of mitochondrial genes in which the T3394Y (p.H30Y) site transitioned from histidine (His.; H) to tyrosine (Tyr.; Y) in the NADH dehydrogenase subunit 1 (ND1) gene. The R11,807G (p.T350A) site transitioned from threonine (Thr.; T) to alanine (Ala.; A). Additionally, the G15,438R or A (p.G231D) site transitioned from glycine (Gly.; G) to aspartic acid (Asp.; D) in cytochrome b (CYTB). Furthermore, pathway analysis, using RNA-seq, confirmed the common mutant pathway between RCC and adrenal carcinoma as cytokine-cytokine receptor (CCR) interaction. Confirmation of the original mutation sites suggests that transfer to AG may be related to the CCR interaction. Thus, during metastasis to the AG, mitochondria DNA mutation may represent the initial origin of the metastasis, followed by the likely mutation of the nuclear genes.

5.
PLoS One ; 15(11): e0242789, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33237957

RESUMO

There has been an increase in the usage of heat-not-burn (HNB) cigarette products. However, their effects on alveolar epithelial cells (AECs) remain unknown. AECs are the target cells of conventional cigarette smoking-related respiratory diseases such as chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis and lung cancer whose pathogenesis involves oxidative stress. In this study, primary rat AECs were isolated, cultured and stimulated by HNB cigarette smoke extract (CSE). Our data indicate that rat AECs exposed to HNB CSE induced oxidative stress response genes (e.g. Hmox-1, Gsta1, Gsta3 and Nqo1). We also compared the oxidative stress response between two different types of AECs, alveolar type I-like (ATI-like) cells and type II (ATII) cells, and between two different types of cigarette, HNB cigarettes and conventional cigarettes. The expressions of Gsta1, Gsta3 and Nqo1 were higher in ATII cells than ATI-like cells in response to HNB and conventional cigarettes, but there was no significant difference in their expression levels between HNB cigarette and conventional cigarette. Taken together, our results suggest that HNB cigarettes have the similar potential as conventional cigarette products to induce oxidative stress response in AECs.


Assuntos
Células Epiteliais Alveolares/efeitos dos fármacos , Fumar Cigarros/efeitos adversos , Estresse Oxidativo/efeitos dos fármacos , Alvéolos Pulmonares/efeitos dos fármacos , Células Epiteliais Alveolares/patologia , Animais , Modelos Animais de Doenças , Sistemas Eletrônicos de Liberação de Nicotina , Temperatura Alta/efeitos adversos , Humanos , Oxirredução/efeitos dos fármacos , Cultura Primária de Células , Alvéolos Pulmonares/patologia , Doença Pulmonar Obstrutiva Crônica/induzido quimicamente , Ratos , Fumaça/efeitos adversos , Nicotiana/efeitos adversos
6.
J Bacteriol ; 194(13): 3541-2, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22689232

RESUMO

Rubrivivax gelatinosus is a facultative photoheterotrophic betaproteobacterium living in freshwater ponds, sewage ditches, activated sludge, and food processing wastewater. There have not been many studies on photosynthetic betaproteobacteria. Here we announce the complete genome sequence of the best-studied phototrophic betaproteobacterium, R. gelatinosus IL-144 (NBRC 100245).


Assuntos
Betaproteobacteria/classificação , Betaproteobacteria/genética , Genoma Bacteriano , Processos Fototróficos , Análise de Sequência de DNA , Betaproteobacteria/isolamento & purificação , Betaproteobacteria/fisiologia , DNA Bacteriano/genética , Água Doce/microbiologia , Gelatina/metabolismo , Dados de Sequência Molecular , Eliminação de Resíduos Líquidos/métodos
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