[LRP16基因功能的生物信息学分析]。

Bo Yang, Xue-Chun Lu, Xiao-Hua Chi, Wei-Dong Han, Li Yu, Fang-Ding Lou
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引用次数: 4

摘要

背景与目的:LRP16是最近发现的与白血病相关的人类新基因。然而,其生物学功能至今尚未完全阐明。本研究旨在通过数据库辅助生物信息学分析,探讨人LRP16基因的生物学功能。方法:采用生物信息学预测方法分析LRP16基因启动子及其编码蛋白的结构和功能,并进行进一步的实验检验。构建pGL3-basic和LRP16启动子亚克隆重组体进行荧光素酶活性分析。构建重组LRP16开放阅读框编码序列和pcDNA3.1真核表达载体,分别转染HL-60和K562细胞系。采用单细胞凝胶电泳法观察紫外线照射后HL-60细胞的DNA损伤情况。流式细胞术分析K562细胞的细胞周期。结果:LRP16启动子是典型的II类真核启动子,其核心调控序列位于转录起始位点上游- 600bp。此外,还发现了7个可能参与细胞周期、造血调节、细胞增殖和DNA损伤修复的顺式作用元件。长型LRP16编码蛋白含有与人组蛋白H2A1C同源的hismacro、COG2110和A1pp序列,残基在148 ~ 315个氨基酸之间。与空质粒对照组相比,lrp16过表达组辐照后HL-60细胞中彗星细胞数量和彗尾长度显著减少,活细胞数量显著增加。与空质粒对照组相比,过表达lrp16的K562组细胞增殖率、G2/M期和S期的比例或数量均显著增加。lrp16在K562细胞中的过表达促进细胞G1期向S期过渡,细胞增殖平台期提前。结论:基于生物信息学的启动子调控预测和蛋白结构域分析有助于基因功能的研究。LRP16可能通过促进细胞增殖、调节细胞周期和拮抗辐射诱导的DNA损伤在白血病进展中发挥重要作用。
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[LRP16 gene function based on bioinformatic analysis].

Background and objective: LRP16 is a human novel gene linked to leukemia identified recently. However, its biological function is not fully clarified so far. This study was to investigate the biological function of human LRP16 gene by database-aided bioinformatics analysis.

Methods: The structures and functions of LRP16 gene promoter and its coding protein were analyzed using bioinformatics prediction, and further experimental testing was performed. The recombinants of pGL3-basic and LRP16 promoter subclones were constructed for luciferase activity analysis. The recombinant of LRP16 open reading frame coding sequence and pcDNA3.1 eukaryotic expression vector was established and transfected into HL-60 and K562 cell lines. DNA damage of HL-60 cells after ultraviolet irradiation was evaluated using single cell gel electrophoresis. Cell cycle of K562 cells was analyzed by flow cytometry.

Results: LRP16 promoter was a typical class II eukaryotic promoter and its core regulation sequence was located within upstream -600 bp of transcriptional start site. In addition, seven cis-acting elements, which may be implicated in cell cycle, hematopoiesis regulation, cell proliferation and repair of DNA damage, were identified. Long type LRP16 coding protein contained homologous sequences of hismacro, COG2110, and A1pp with human histone H2A1C between 148 and 315 amino acid residue. The number of comet cells and the length of comet tail in HL-60 cells irradiated were significantly decreased and the number of living cell was significantly increased in LRP16-overexpression group compared with empty plasmid control group. The proliferation rate and ratio or quantity of G2/M and S phases were significantly increased in LRP16-overexpression K562 group compared with empty plasmid control group. LRP16-overexpression in K562 cells promoted the transition of G1 to S phase and plateau phase of cell proliferation was advanced.

Conclusions: Promoter regulation prediction and protein domain analysis based on bioinformatics contribute to the study of gene function. LRP16 may play an important role in leukemia progression by promoting cell proliferation, regulating cell cycle, and antagonizing radiation-induced DNA damage.

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