CN114369623A - A Synaptotagmin2-RNAi Based on Cre-lox Recombination System and Its Application - Google Patents
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Abstract
Translated fromChinese
Description
Translated fromChinese技术领域technical field
本发明属于生物医学技术领域，尤其涉及一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用。The invention belongs to the technical field of biomedicine, in particular to a Synaptotagmin2-RNAi based on Cre-lox recombination system and its application.
背景技术Background technique
1.RNA干扰技术：1. RNA interference technology:
RNA干扰（RNA interference，RNAi）是指在进化过程中高度保守的、由双链RNA（double-stranded RNA，dsRNA）诱发的、和同源mRNA高效特异性降解的现象。由于使用RNAi技术可以特异性降低或关闭特定基因在细胞或有机体中的表达，所以该技术已被广泛用于探索基因功能和传染性疾病及恶性肿瘤的基因治疗领域。人们也基于这一现象研究了一种反向调控基因表达的遗传学机制。在动物中，RNAi可以通过U6启动表达shRNA来实现。目前的U6载体可以通过2种方式在动物细胞内表达：瞬时表达以及稳定表达。稳定表达主要是通过插入基因组中实现的。RNA interference (RNAi) refers to a phenomenon that is highly conserved during evolution, induced by double-stranded RNA (dsRNA), and homologous mRNA is efficiently and specifically degraded. Since the use of RNAi technology can specifically reduce or shut down the expression of specific genes in cells or organisms, this technology has been widely used in the field of gene therapy to explore gene function and infectious diseases and malignant tumors. A genetic mechanism of reverse regulation of gene expression has also been studied based on this phenomenon. In animals, RNAi can be achieved by expressing shRNA through the U6 promoter. The current U6 vector can be expressed in animal cells in two ways: transient expression and stable expression. Stable expression is mainly achieved by insertion into the genome.
2.Cre-lox技术：2.Cre-lox technology:
Cre-lox技术是20世纪80年代从P1噬菌体中发现的一种位点特异性重组技术。该技术可通过Cre重组酶和lox位点的相互作用，实现目的片段的删除、翻转、插入和易位等。该技术不需要借助任何辅助因子，可作用于多种结构的DNA底物，如线形、环状甚至超螺旋DNA等，操作简单、快速、高效，因此被广泛应用于真核生物和原核生物的基因敲除、插入、翻转和易位等研究中。目前，Cre-lox系统应用最热门的领域是基因打靶，已被证明是哺乳动物细胞和小鼠遗传操作最有用的工具，该系统和基因打靶的结合提供了实现条件基因敲除或激活的手段。Cre-lox technology is a site-specific recombination technology discovered from P1 phage in the 1980s. This technology can achieve deletion, inversion, insertion and translocation of target fragments through the interaction of Cre recombinase and lox sites. This technology does not require any cofactors and can act on DNA substrates of various structures, such as linear, circular and even supercoiled DNA. The operation is simple, fast and efficient, so it is widely used in eukaryotes and prokaryotes. Gene knockout, insertion, inversion, and translocation studies. Currently, the most popular field of application of the Cre-lox system is gene targeting, which has been proven to be the most useful tool for genetic manipulation of mammalian cells and mice. The combination of this system and gene targeting provides a means to achieve conditional gene knockout or activation .
3.病毒依赖的基因重组3. Virus-dependent genetic recombination
由于转基因动物依赖的基因重组存在耗时长、成本高、区域或者组织特异性不高等不足。采用比较灵活的方式使用Cre-lox系统，例如通过病毒引入Cre或loxP元件，从而实现基因重组。借助病毒表达的cre-lox重组系统，可以特异性对某些细胞的标记和操控。当前运用神经示踪技术对大脑特定神经环路的结构和功能进行解析时，运用 Cre重组酶系统和 AAV血清型（比如 rAAV2/9、rAAV2/retro、rAAV2/1）结合，达到特异性对神经环路标记和功能研究的目的：病毒可以通过局部注射的方式保证区域特异性感染，再加上驱动 Cre基因的特异性启动子，能够实现更强的区域和细胞特异性的基因重组。但是对于如何时空特异性地干扰特定的神经环路的功能，需要涉及一种更优的时空特异调控相关重要基因的表达工具的开发。Due to genetic recombination dependent on transgenic animals, there are disadvantages such as time-consuming, high cost, and low region or tissue specificity. The Cre-lox system is used in a more flexible way, such as introducing Cre or loxP elements through a virus, thereby realizing gene recombination. With the help of the virus-expressed cre-lox recombination system, certain cells can be specifically labeled and manipulated. At present, when using neural tracer technology to analyze the structure and function of specific neural circuits in the brain, the Cre recombinase system is used to combine with AAV serotypes (such as rAAV2/9, rAAV2/retro, rAAV2/1) to achieve specific neural The purpose of loop labeling and function research: The virus can ensure region-specific infection through local injection, and coupled with the specific promoter driving the Cre gene, it can achieve stronger region- and cell-specific gene recombination. However, for how to specifically interfere with the function of specific neural circuits in space and time, it is necessary to develop a better expression tool that specifically regulates related important genes in space and time.
发明内容SUMMARY OF THE INVENTION
本发明实施例的目的在于提供一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用，旨在解决背景技术提出的问题。The purpose of the embodiments of the present invention is to provide a Synaptotagmin2-RNAi based on the Cre-lox recombination system and its application, and to solve the problems raised by the background art.
本发明实施例是这样实现的，一种基于Cre-lox重组系统的Synaptotagmin2-RNAi，包括一种Cre酶依赖的rAAV表达的RNAi表达载体，所述的Cre酶依赖的rAAV表达的RNAi表达载体包含顺次连接的：AAV2ITR，兴奋性神经元表达的启动子CaMKIIα，Cre酶依赖的RNAi表达盒，Syt2 RNAi发卡结构插入位点，WPRE，bGHpoly（A）signal和AAV2ITR。The embodiments of the present invention are achieved in this way, a Synaptotagmin2-RNAi based on the Cre-lox recombination system, includes a Cre enzyme-dependent rAAV expression RNAi expression vector, and the Cre enzyme-dependent rAAV expression RNAi expression vector includes Sequentially linked: AAV2ITR, promoter CaMKIIα expressed by excitatory neurons, Cre enzyme-dependent RNAi expression cassette, Syt2 RNAi hairpin insertion site, WPRE, bGHpoly(A) signal and AAV2ITR.
进一步的技术方案，所使用的的Syt2 shRNA 的具体序列为：Further technical scheme, the specific sequence of the used Syt2 shRNA is:
5’-CCCTTTGACCCTCAGTGAT-3’。5'-CCCTTTGACCCTCAGTGAT-3'.
对照组Scramble shRNA的具体序列为：The specific sequence of the Scramble shRNA in the control group is:
5’-GGTTTATATCGCGGTTATT -3’。5'-GGTTTATATCGCGGTTATT-3'.
本发明实施例的另一目的在于，一种基于Cre-lox重组系统的Synaptotagmin2-RNAi的应用，将所述的Synaptotagmin2-RNAi应用于重组病毒pAAV2-CaMKIIα-DIO-(mCherry-bGH polyA-U6)-shRNA(Syt2/Scramble)-WPRE -hGH polyA的制备。Another object of the embodiment of the present invention is to apply the Synaptotagmin2-RNAi based on the Cre-lox recombination system to the recombinant virus pAAV2-CaMKIIα-DIO-(mCherry-bGH polyA-U6) - Preparation of shRNA(Syt2/Scramble)-WPRE-hGH polyA.
进一步的技术方案，将所述的重组病毒pAAV2-CaMKIIα-DIO-(mCherry-bGHpolyA-U6)-shRNA(Syt2/Scramble)-WPRE-hGH polyA 注射到小鼠岛叶，并将辅助病毒AAV2/R-hSyn-cre-WPRE-hGH polyA注射到小鼠基底外侧杏仁核，待病毒表达四周后，观察腓总神经结扎模型小鼠的后足底机械痛阈值。Further technical scheme, the described recombinant virus pAAV2-CaMKIIα-DIO-(mCherry-bGHpolyA-U6)-shRNA(Syt2/Scramble)-WPRE-hGH polyA is injected into mouse insula, and the helper virus AAV2/R -hSyn-cre-WPRE-hGH polyA was injected into the basolateral amygdala of mice, and after the virus was expressed for four weeks, the mechanical pain threshold of the posterior plantar of the mice with common peroneal nerve ligation was observed.
本发明实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用，通过腺相关病毒依赖的Cre-lox重组系统，对特定脑区Synaptotagmin-2 分子进行shRNA干扰，从而应用于镇痛治疗。本发明在生物信息学分析的基础上，发现小鼠痛模型中高表达的突触传递相关蛋白Synaptotagmin 2 （简称Syt2：是一种钙结合蛋白，有助于钙离子触发中枢和神经肌肉突触的快速神经递质释放，在神经系统的多个脑区都有表达），因此构建了shRNA干扰策略，可有效缓解痛模型动物的伤害性感受，本发明将为靶向镇痛治疗提供方向。A kind of Synaptotagmin2-RNAi based on Cre-lox recombination system and its application provided in the embodiment of the present invention, through the Cre-lox recombination system dependent on adeno-associated virus, shRNA interference is performed on Synaptotagmin-2 molecules in specific brain regions, so as to be applied to the anti-inflammatory drugs Pain treatment. Based on bioinformatics analysis, the present invention finds that the highly expressed synaptic transmission-related protein Synaptotagmin 2 (Syt2 for short: is a calcium-binding protein in the mouse pain model), which is helpful for calcium ions to trigger central and neuromuscular synapses. Rapid release of neurotransmitters, which are expressed in multiple brain regions of the nervous system), so the shRNA interference strategy is constructed, which can effectively relieve the nociception of pain model animals, and the present invention will provide a direction for targeted analgesic therapy.
附图说明Description of drawings
图1为本发明实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用中的痛模型小鼠IC和BLA脑区Syt2分子表达情况。Fig. 1 is a kind of Synaptotagmin2-RNAi based on Cre-lox recombination system provided in the embodiment of the present invention and the expression of Syt2 molecules in IC and BLA brain regions of pain model mice in its application.
图2为本发明实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用中的Syt2荧光素酶检测图。FIG. 2 is a detection diagram of Syt2 luciferase in a Synaptotagmin2-RNAi based on a Cre-lox recombination system and its application provided by an embodiment of the present invention.
图3为本发明实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用中的病毒注射示意图。FIG. 3 is a schematic diagram of a Cre-lox recombination system-based Synaptotagmin2-RNAi and virus injection in its application according to an embodiment of the present invention.
图4为本发明实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi及其应用中的行为学检测结果。Fig. 4 is a kind of Synaptotagmin2-RNAi based on Cre-lox recombination system and the behavioral detection result in its application provided by the embodiment of the present invention.
具体实施方式Detailed ways
为了使本发明的目的、技术方案及优点更加清楚明白，以下结合附图及实施例，对本发明进行进一步详细说明。应当理解，此处所描述的具体实施例仅仅用以解释本发明，并不用于限定本发明。In order to make the objectives, technical solutions and advantages of the present invention clearer, the present invention will be further described in detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are only used to explain the present invention, but not to limit the present invention.
以下结合具体实施例对本发明的具体实现进行详细描述。The specific implementation of the present invention will be described in detail below with reference to specific embodiments.
本发明一个实施例提供的一种基于Cre-lox重组系统的Synaptotagmin2-RNAi，包括一种Cre酶依赖的rAAV表达的RNAi表达载体，所述的Cre酶依赖的rAAV表达的RNAi表达载体包含顺次连接的：AAV2ITR，兴奋性神经元表达的启动子CaMKIIα，Cre酶依赖的RNAi表达盒，Syt2 RNAi发卡结构插入位点，WPRE，bGHpoly（A）signal和AAV2ITR。An embodiment of the present invention provides a Synaptotagmin2-RNAi based on the Cre-lox recombination system, including a Cre enzyme-dependent rAAV expression RNAi expression vector, and the Cre enzyme-dependent rAAV expression The RNAi expression vector comprises sequential Connected: AAV2ITR, promoter CaMKIIα expressed by excitatory neurons, Cre enzyme-dependent RNAi expression cassette, Syt2 RNAi hairpin insertion site, WPRE, bGHpoly(A) signal and AAV2ITR.
所使用的Syt2 shRNA 的具体序列为：5’-CCCTTTGACCCTCAGTGAT-3’，对照Scramble shRNA的具体序列为：5’-GGTTTATATCGCGGTTATT -3’。The specific sequence of the Syt2 shRNA used was: 5'-CCCTTTGACCCTCAGTGAT-3', and the specific sequence of the control Scramble shRNA was: 5'-GGTTTATATCGCGGTTATT-3'.
小鼠痛觉模型实验的具体步骤包括：The specific steps of the mouse pain model experiment include:
1.建立小鼠腓总神经结扎（common peroneal nerve ligation，CPNL）模型：小鼠通过2%异氟醚麻醉后，在左腿做切口暴露腓总神经，无菌手术线结扎腓总神经后局部缝合消毒，待动物清醒后放回笼中饲养。假手术组仅暴露腓总神经，但不进行结扎。1. Establish a mouse model of common peroneal nerve ligation (CPNL): After the mice were anesthetized with 2% isoflurane, an incision was made in the left leg to expose the common peroneal nerve, and the common peroneal nerve was ligated locally with sterile surgical thread. The sutures were sterilized, and the animals were put back into the cages after they were awake. In the sham operation group, only the common peroneal nerve was exposed without ligation.
2.机械痛检测：动物手术前使用von-frey丝（克数为0.008g，0.02g，0.04g，0.16g，0.4g，0.6g，1g，1.4g以及2g）检测左足机械痛阈值，记为第0天数据，手术后从第1天开始，每天固定时间检测左足机械痛阈值，并进行统计学分析。2. Detection of mechanical pain: Before the operation of animals, von-frey silk (grams of 0.008g, 0.02g, 0.04g, 0.16g, 0.4g, 0.6g, 1g, 1.4g and 2g) was used to detect the mechanical pain threshold of the left foot. The data on the 0th day, from the 1st day after the operation, the left foot mechanical pain threshold was detected at a fixed time every day, and statistical analysis was performed.
3.蛋白印迹分析：动物术后第7天，麻醉分离大脑，对右侧IC和BLA脑区进行取材提蛋白，对Syt2等蛋白表达进行半定量分析（结果如图1所示）。3. Western blot analysis: On the 7th day after the operation, the animals were anesthetized to separate the brain, and the right IC and BLA brain regions were extracted for protein extraction, and the expression of Syt2 and other proteins was semi-quantitatively analyzed (the results are shown in Figure 1).
4.病毒构建与注射：委托武汉枢密公司构建重组腺相关病毒pAAV2-CaMKIIα-DIO-(mCherry-bGH-polyA-U6)-shRNA(Syt2/Scramble)-WPRE-hGH polyA和辅助病毒，在HEK293细胞对shRNA进行验证，结果如图2所示。随后将该病毒注射在小鼠右侧IC (注射量为200nl，病毒滴度>1012)，将辅助病毒AAV2/R-hSyn-cre-WPRE-hGH polyA注射在小鼠右侧BLA(注射量为200nl，病毒滴度>1012)，注射方法如图3所示。4. Virus construction and injection: Entrusted Wuhan Shumi Company to construct recombinant adeno-associated virus pAAV2-CaMKIIα-DIO-(mCherry-bGH-polyA-U6)-shRNA(Syt2/Scramble)-WPRE-hGH polyA and helper virus, in HEK293 cells The shRNA was verified, and the results are shown in Figure 2. The virus was then injected into the right IC of the mouse (the injection volume was 200 nl, and the virus titer was >1012 ), and the helper virus AAV2/R-hSyn-cre-WPRE-hGH polyA was injected into the right BLA of the mouse (injection volume was >10 12 ). 200nl, virus titer>1012 ), the injection method is shown in Figure 3.
5.动物行为学检测：病毒表达4周后，建立腓总神经结扎模型，检测小鼠左后足机械痛阈值，对各组动物痛阈进行统计学分析，如图4所示：注射shRNA（Syt2）的痛觉模型动物痛阈明显上升，而注射shRNA（Scramble）的痛觉模型动物痛阈相比于无病毒注射组没有明显改变，通过shRNA降低IC-BLA神经通路上的Syt2分子表达，可以有效镇痛。5. Animal behavioral detection: After 4 weeks of virus expression, the common peroneal nerve ligation model was established, the mechanical pain threshold of the left hind foot of mice was detected, and the pain threshold of each group of animals was statistically analyzed, as shown in Figure 4: injection of shRNA ( Syt2) pain model animals significantly increased pain threshold, while the pain threshold of pain model animals injected with shRNA (Scramble) did not change significantly compared with the no-virus injection group. Reducing the expression of Syt2 molecules on the IC-BLA neural pathway by shRNA can effectively Pain relief.
以上所述仅为本发明的较佳实施例而已，并不用以限制本发明，凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等，均应包含在本发明的保护范围之内。The above descriptions are only preferred embodiments of the present invention and are not intended to limit the present invention. Any modifications, equivalent replacements and improvements made within the spirit and principles of the present invention shall be included in the protection of the present invention. within the range.
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