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Gene Expr Patterns ; 28: 95-103, 2018 06.
Artigo em Inglês | MEDLINE | ID: mdl-29571919

RESUMO

22q11.2 deletion syndrome (22q11.2DS) carries increased risk for both physical and psychiatric symptoms, including a high risk for schizophrenia. Understanding the genetic elements within the deletion region therefore has the potential to unlock the mysteries of both diseases. While most of the protein-coding genes in this region have been characterized, novel elements, such as non-coding RNAs and small Open Reading Frames (sORFs) remain unstudied. We have identified a novel, highly-conserved mouse sORF in a region of the mouse genome that is orthologous to a portion of the 22q11.2 deletion. This region was previously associated with age-dependent synaptic plasticity abnormalities. We refer to it as the Plasticity Associated Neural Transcript Short, or Pants. In developing and aging mouse brain, Pants expression is strongest in hippocampus, especially in areas CA3 and CA2, throughout the dorsoventral axis. The Pants peptide is expressed throughout the hippocampus, with an age-dependent increase in stratum lucidum at 16 weeks of age. This expression pattern suggests a potential role for Pants in many hippocampal behaviors, as well as a potential role in the age-dependent neurologic deficits displayed by 22q11.2DS model mice and patients.


Assuntos
Encéfalo/metabolismo , Deleção Cromossômica , Síndrome de DiGeorge/genética , Fases de Leitura Aberta/genética , Fragmentos de Peptídeos/metabolismo , Fatores Etários , Animais , Síndrome de DiGeorge/metabolismo , Síndrome de DiGeorge/patologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout
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