Carlson Kimberly A, Gardner Kylee, Pashaj Anjeza, Carlson Darby J, Yu Fang, Eudy James D, Zhang Chi, Harshman Lawrence G
Biology Department, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Genet Res Int. 2015;2015:835624. doi: 10.1155/2015/835624. Epub 2015 May 21.
Aging is a complex process characterized by a steady decline in an organism's ability to perform life-sustaining tasks. In the present study, two cages of approximately 12,000 mated Drosophila melanogaster females were used as a source of RNA from individuals sampled frequently as a function of age. A linear model for microarray data method was used for the microarray analysis to adjust for the box effect; it identified 1,581 candidate aging genes. Cluster analyses using a self-organizing map algorithm on the 1,581 significant genes identified gene expression patterns across different ages. Genes involved in immune system function and regulation, chorion assembly and function, and metabolism were all significantly differentially expressed as a function of age. The temporal pattern of data indicated that gene expression related to aging is affected relatively early in life span. In addition, the temporal variance in gene expression in immune function genes was compared to a random set of genes. There was an increase in the variance of gene expression within each cohort, which was not observed in the set of random genes. This observation is compatible with the hypothesis that D. melanogaster immune function genes lose control of gene expression as flies age.
衰老 是一个复杂的过程,其特征是生物体执行维持生命任务的能力稳步下降。在本研究中,使用两笼约12,000只已交配的黑腹果蝇雌性作为随着年龄频繁采样的个体的RNA来源。微阵列数据分析采用线性模型方法来校正盒效应;该方法鉴定出1581个候选衰老基因。使用自组织映射算法对这1581个显著基因进行聚类分析,确定了不同年龄阶段的基因表达模式。参与免疫系统功能和调节、绒毛膜组装和功能以及代谢的基因均随着年龄的增长而有显著差异表达。数据的时间模式表明,与衰老相关的基因表达在寿命早期就受到影响。此外,将免疫功能基因的基因表达时间方差与一组随机基因进行了比较。每个队列中基因表达的方差都有所增加,而在随机基因集中未观察到这种情况。这一观察结果与黑腹果蝇免疫功能基因随着果蝇衰老而失去对基因表达控制的假设相符。