Highly Specific and Quantitative Gene Expression Profiling Based on DNA Computing
نویسندگان
چکیده
DNA chips and microarrays have been used to simultaneously analyze the expression profiling of many genes [1, 2]. In the analysis, the two-color method [3] is generally employed to determine the relative expression levels between two samples. However, not only the relative expression levels between target genes in a sample but also the absolute expression level of each target gene in a sample cannot be determined accurately with conventional DNA chips and microarrays combined with the two-color method. This hinders extensive and quantitative analysis of gene expression profiling data using bioinformatics. Here, we introduce a gene expression profiling method based on DNA computing, which enable us to know the absolute amount of target gene transcripts.
منابع مشابه
Induced Acidic chitinase Expression and Scab-Resistant in Wheat Under Field Condition
Fusarium head blight (FHB) caused by Fusarium graminearum is responsible for billions of dollars in agriculture losses. The goal of the present study was evaluation the expression of acidic chitinase, one of PR proteins, in wheat defense response against different FHB induced treatments in 'Falat' as a highly susceptible and 'Sumai3' as a tolerant cultivar. These treatments contained fungi extr...
متن کاملGSK3β and CREB3 Gene Expression Profiling in Benign and Malignant Salivary Gland Tumors
Background: Salivary gland tumors (SGT) are rare lesions with uncertain histopathology. One of the major signaling pathways that participate in the development of several tumors is protein kinase A. In this pathway, glycogen synthase kinase β (GSK3β) and cAMP responsive element binding protein (CREB3) are two genes which are supposed to be down regulated in most human tumors. The expression lev...
متن کاملValidation of a genus-specific gene; TPS, used as internal control in quantitative Real Time PCR of transgenic cotton
Identification of genes with invariant levels of gene expression is a prerequisite for validating transcriptomic changes accompanying development. Ideally expression of these genes should be independent of the morphogenetic process or environmental condition.We report here the validation of internal control gene i.e.TPS (trehalose 6-phosphate-synthase) in cotton (Gossypium spp), using TaqMan sy...
متن کاملGene Expression Analysis by DNA Computing
DNA chips perform the rapid, parallel detection of a target set of gene transcripts through specific hybridization of targets to DNA probes integrated on the chip surface [1]. A DNA chip can thus be considered as a special purpose DNA computer for parallel homology search. Conventional DNA chips rely solely on hybridization for transcript detection. As a result, the recognition process for geno...
متن کاملImproved quantitative real-time RT-PCR for expression profiling of individual cells.
The real-time quantitative polymerase chain reaction (rtqPCR) has overcome the limitations of conventional, time-consuming quantitative PCR strategies and is maturing into a routine tool to quantify gene expression levels, following reverse transcription (RT) of mRNA into complementary DNA (cDNA). Expression profiling with single-cell resolution is highly desirable, in particular for complex ti...
متن کامل