相关实验视频
Updated: Mar 29, 2026

13:10
Use of Alu Element Containing Minigenes to Analyze Circular RNAs
Published on: March 10, 2020
7.8K
概括
重复序列的基因表达在海胚胎和成年细胞之间有所不同. 这突出了细胞特异性模式在核RNA中重复的DNA序列的表示.
科学领域:
- 分子生物学分子生物学
- 发展生物学 发展生物学
- 基因组学就是基因组学.
背景情况:
- 在真核生物基因组中,重复性的DNA序列是丰富的.
- 重复序列及其转录的功能意义尚未完全理解.
- 不同基因表达对细胞分化和发育至关重要.
研究的目的:
- 为了研究不同类型的海细胞核RNA中克隆的重复DNA序列的定量表示.
- 为了确定重复序列转录模式是否是细胞特异的.
- 探索重复序列与核RNA复杂性之间的关系.
主要方法:
- 标记的克隆重复序与来自海胃胚胎和成年肠道的RNA混合.
- 使用RNA过量杂交动力学和DNA过量定位测量转录度.
- 对线程表示和转录大小的分析.
主要成果:
- 观察到不同重复序列家族的转录水平有显著的定量变化.
- 高度表示的重复序列的集合在胃肠和肠核RNA之间有所不同.
- 所有克隆重复的两个链都被转录,每个链的水平一般都相似.
结论:
- 核RNA中重复序列表示的定量模式是特定于细胞类型的.
- 这种差异表示表明重复序列在细胞特异性核RNA代谢中的作用.
- 重复序列的转录在核RNA中发现,而不是多体信使RNA,并且是大型分子.
相关概念视频
RACE - Rapid Amplification of cDNA Ends
7.6K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
7.6K
RNA-seq
12.5K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
12.5K
Complementary DNA
32.2K
Overview
32.2K

