跳到主要导航 跳到搜索 跳到主要内容

Bioinformatic prediction and functional characterization of human KIAA0100 gene

  • He Cui
  • , Xi Lan
  • , Shemin Lu
  • , Fujun Zhang
  • , Wanggang Zhang
  • Xi'an Jiaotong University

科研成果: 期刊稿件 › 文章 › 同行评审

10 引用 (Scopus)

摘要

Our previous study demonstrated that human KIAA0100 gene was a novel acute monocytic leukemia-associated antigen (MLAA) gene. But the functional characterization of human KIAA0100 gene has remained unknown to date. Here, firstly, bioinformatic prediction of human KIAA0100 gene was carried out using online softwares; Secondly, Human KIAA0100 gene expression was downregulated by the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) 9 system in U937 cells. Cell proliferation and apoptosis were next evaluated in KIAA0100-knockdown U937 cells. The bioinformatic prediction showed that human KIAA0100 gene was located on 17q11.2, and human KIAA0100 protein was located in the secretory pathway. Besides, human KIAA0100 protein contained a signalpeptide, a transmembrane region, three types of secondary structures (alpha helix, extended strand, and random coil), and four domains from mitochondrial protein 27 (FMP27). The observation on functional characterization of human KIAA0100 gene revealed that its downregulation inhibited cell proliferation, and promoted cell apoptosis in U937 cells. To summarize, these results suggest human KIAA0100 gene possibly comes within mitochondrial genome; moreover, it is a novel anti-apoptotic factor related to carcinogenesis or progression in acute monocytic leukemia, and may be a potential target for immunotherapy against acute monocytic leukemia.

源语言英语
页(从-至)10-18
页数9
期刊Journal of Pharmaceutical Analysis
卷7
期1
DOI
出版状态已出版 - 1 2月 2017

学术指纹

探究 'Bioinformatic prediction and functional characterization of human KIAA0100 gene' 的科研主题。它们共同构成独一无二的学术指纹。

引用此