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CRISPR and Stem Cell Research Literatures

机译:CRISPR和干细胞研究文献

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Stem cells are derived from embryonic and non-embryonic tissues. Most stem cell studies are for animal stem cells and plants have also stem cell. Stem cells were discovered in 1981 from early mouse embryos. Stem cells have the potential to develop into all different cell types in the living body. Stem cell is a body repair system. When a stem cell divides it can be still a stem cell or become adult cell, such as a brain cell. Stem cells are unspecialized cells and can renew themselves by cell division, and stem cells can also differentiate to adult cells with special functions. Stem cells replace the old cells and repair the damaged tissues. Embryonic stem cells can become all cell types of the body because they are pluripotent. Adult stem cells are thought to be limited to differentiating into different cell types of their tissue of origin. CRISPR (clustered regularly interspaced short palindromic repeats ) is a family of DNA sequences found within the genomes of prokaryotic organisms such as bacteria and archaea. These sequences are derived from DNA fragments from viruses that have previously infected the prokaryote and are used to detect and destroy DNA from similar viruses during subsequent infections. Hence these sequences play a key role in the antiviral defense system of prokaryotes. Cas9 is an enzyme that uses CRISPR sequences as a guide to recognize and cleave specific strands of DNA that are complementary to the CRISPR sequence. Cas9 enzymes together with CRISPR sequences form the basis of a technology known as CRISPR/Cas9 that can be used to edit genes within organisms. This type of gene editing process has a wide variety of applications including use as a basic biology research tool, development of biotechnology products, and potentially to treat diseases. The CRISPR/Cas system is a prokaryotic immune system that confers resistance to foreign genetic elements such as those present within plasmids and phages that provides a form of acquired immunity. RNA harboring the spacer sequence helps Cas proteins recognize and cut foreign pathogenic DNA. Other RNA-guided Cas proteins cut foreign RNA. CRISPR are found in approximately 50% of sequenced bacterial genomes and nearly 90% of sequenced archaea. This article introduces recent research reports as.
机译:干细胞来源于胚胎和非胚胎组织。大多数干细胞研究都是针对动物干细胞,而植物也有干细胞。 1981年从早期小鼠胚胎中发现了干细胞。干细胞具有发展为生物体内所有不同细胞类型的潜力。干细胞是一种身体修复系统。当干细胞分裂时,它仍然可以是干细胞或变成成年细胞,例如脑细胞。干细胞是非专业细胞,可以通过细胞分裂而自我更新,干细胞也可以分化为具有特殊功能的成年细胞。干细胞替代旧细胞并修复受损的组织。胚胎干细胞是多能的,因此可以成为人体的所有细胞类型。成人干细胞被认为仅限于分化成其起源组织的不同细胞类型。 CRISPR(成簇的规则间隔的短回文重复序列)是在细菌和古细菌等原核生物的基因组中发现的DNA序列家族。这些序列来自先前感染过原核生物的病毒的DNA片段,并用于在随后的感染过程中检测和破坏相似病毒的DNA。因此,这些序列在原核生物的抗病毒防御系统中起关键作用。 Cas9是一种酶,使用CRISPR序列作为指导来识别和切割与CRISPR序列互补的特定DNA链。 Cas9酶与CRISPR序列一起构成了称为CRISPR / Cas9的技术的基础,该技术可用于编辑生物体内的基因。这种类型的基因编辑过程具有广泛的应用,包括用作基础生物学研究工具,开发生物技术产品以及潜在地治疗疾病。 CRISPR / Cas系统是原核免疫系统,它赋予对外源遗传元件(如质粒和噬菌体内存在的外源遗传元件)的抗性,以提供获得性免疫的形式。带有间隔区序列的RNA有助于Cas蛋白识别和切割外源致病DNA。其他RNA引导的Cas蛋白可切割外源RNA。在大约50%的测序细菌基因组和近90%的测序古细菌中发现CRISPR。本文介绍了最新的研究报告。

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