哺乳动物复原病毒样蛋白PEG10包装了自己的mRNA,可以伪型为mRNA传递
Michael Segel1,2,3,4,5, Blake Lash1,2,3,4,5, Jingwei Song1,2,3,4,5
1Howard Hughes Medical Institute, Cambridge, MA 02139, USA.
概括
科学家重新使用病毒基因PEG10,使用一种名为选择性内源封装细胞传递 (SEND) 的新系统来包装和传递特定的RNA. 这为治疗RNA提供了一个新平台.
科学领域:
- 基因组学
- 分子生物学
- 病毒学
背景情况:
- 细胞基因组包含化的病毒基因,包括来自逆转移体和逆转移体的Gag同类基因.
- 哺乳动物的基因组含有类似于病毒的Gag同类分子.
研究的目的:
- 调查哺乳动物口腔同类的功能,特别是PEG10.
- 根据PEG10的特性开发一种新的RNA传递系统.
主要方法:
- 已识别的哺乳动物口腔同类物,包括LTR逆转移素同类物PEG10.
- 标志着PEG10结合和分泌自己的mRNA的能力.
- 设计了小鼠和人类的PEG10来包装和传递特定的RNA,从而创建了SEND系统.
主要成果:
- PEG10优先结合并促进其mRNA的囊泡分泌.
- 可以使用其未翻译的区域重新编程PEG10的mRNA载荷.
- 在小鼠和人类细胞中开发了SEND平台,用于特定RNA的包装,分泌和输送.
结论:
- PEG10的mRNA包装和分泌能力是可以重新编程的.
- SEND系统是一个模块化和高效的治疗RNA输送平台.
相关概念视频
Retrovirus Life Cycles
47.7K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
47.7K
Retroviruses
13.2K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
13.2K
LTR Retrotransposons
18.3K
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
18.3K
Non-LTR Retrotransposons
12.2K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
12.2K
Regulated mRNA Transport
6.6K
In eukaryotes, transcription and translation are compartmentalized; an mRNA is first synthesized in the nucleus and then selectively transported to the cytoplasm for protein synthesis. Before transport, a pre-mRNA undergoes several steps of post-transcriptional modifications including splicing, 5' capping, and the addition of a poly-adenine tail. Various proteins bind to the pre-mRNA during these modifications. The mRNA transport takes place with the help of multiple proteins playing...
6.6K
piRNA - Piwi-interacting RNAs
7.1K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
7.1K


