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1.
Am J Hum Genet ; 107(5): 882-894, 2020 11 05.
Artigo em Inglês | MEDLINE | ID: mdl-33022220

RESUMO

Plasma DNA fragmentomics is an emerging area in cell-free DNA diagnostics and research. In murine models, it has been shown that the extracellular DNase, DNASE1L3, plays a role in the fragmentation of plasma DNA. In humans, DNASE1L3 deficiency causes familial monogenic systemic lupus erythematosus with childhood onset and anti-dsDNA reactivity. In this study, we found that human patients with DNASE1L3 disease-associated gene variations showed aberrations in size and a reduction of a "CC" end motif of plasma DNA. Furthermore, we demonstrated that DNA from DNASE1L3-digested cell nuclei showed a median length of 153 bp with CC motif frequencies resembling plasma DNA from healthy individuals. Adeno-associated virus-based transduction of Dnase1l3 into Dnase1l3-deficient mice restored the end motif profiles to those seen in the plasma DNA of wild-type mice. Our findings demonstrate that DNASE1L3 is an important player in the fragmentation of plasma DNA, which appears to act in a cell-extrinsic manner to regulate plasma DNA size and motif frequency.


Assuntos
DNA/genética , Endodesoxirribonucleases/genética , Lúpus Eritematoso Sistêmico/genética , Mutação , Animais , Estudos de Casos e Controles , DNA/sangue , Fragmentação do DNA , Dependovirus/genética , Dependovirus/metabolismo , Modelos Animais de Doenças , Endodesoxirribonucleases/deficiência , Endodesoxirribonucleases/metabolismo , Terapia Genética , Vetores Genéticos/química , Vetores Genéticos/metabolismo , Humanos , Lúpus Eritematoso Sistêmico/enzimologia , Lúpus Eritematoso Sistêmico/patologia , Camundongos , Camundongos Transgênicos , Especificidade por Substrato , Transdução Genética
2.
Epilepsia ; 48(5): 1015-8, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17509004

RESUMO

A previous study conducted in Taiwan found a 100% association between HLA-B*1502 allele and carbamazepine-induced Stevens-Johnson syndrome (SJS) in Han Chinese subjects, with an extremely high odds ratio compared with carbamazepine-tolerant subjects (odds ratio = 2,504). We examined this association in 24 Hong Kong Han Chinese subjects who had cutaneous adverse reactions induced by different antiepileptic drugs (AEDs). They were matched with 48 AED-tolerant controls. HLA-B*1502 was associated with severe cutaneous reactions (SCR) induced by AEDs, which included carbamazepine, phenytoin, and lamotrigine (p = 0.001, odds ratio = 17.6), but was not associated with maculopapular exanthema (MPE) (p = 0.32). Further studies in larger samples of ethnically matched subjects should be conducted to confirm the findings. Identification of genetic polymorphisms predisposing to development of AED-induced SCR offers the possibility of avoiding these high-risk drugs in genetically susceptible individuals.


Assuntos
Anticonvulsivantes/efeitos adversos , Povo Asiático/genética , Toxidermias/etnologia , Toxidermias/etiologia , Epilepsia/tratamento farmacológico , Antígenos HLA-B/genética , Adolescente , Adulto , Alelos , Anticonvulsivantes/uso terapêutico , Carbamazepina/efeitos adversos , Carbamazepina/uso terapêutico , Estudos de Casos e Controles , Criança , Toxidermias/genética , Hipersensibilidade a Drogas/etnologia , Hipersensibilidade a Drogas/genética , Epilepsia/etnologia , Epilepsia/genética , Feminino , Predisposição Genética para Doença/etnologia , Antígeno HLA-B15 , Hong Kong , Humanos , Lamotrigina , Masculino , Pessoa de Meia-Idade , Farmacogenética , Fenitoína/efeitos adversos , Fenitoína/uso terapêutico , Polimorfismo Genético , Síndrome de Stevens-Johnson/induzido quimicamente , Síndrome de Stevens-Johnson/etnologia , Síndrome de Stevens-Johnson/genética , Triazinas/efeitos adversos , Triazinas/uso terapêutico
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