这 CRISPR, 一个 首字母缩略词 成簇规律间隔短回文重复序列(Clustered Regularly Interspaced Short Palindromic Repeats)最早于1987年在大肠杆菌基因组中被发现。这些基因位点由短的重复DNA序列组成,这些序列之间由独特的“间隔区”序列隔开,而这些间隔区序列来源于外源遗传元件。最初被称为SRSR,其生物学功能尚不清楚,但其独特的结构表明它们在原核生物基因组中可能扮演着重要但神秘的角色。

(图片仅供参考)
这 CRISPR, 一个 首字母缩略词 成簇规律间隔短回文重复序列(Clustered Regularly Interspaced Short Palindromic Repeats)最早于1987年在大肠杆菌基因组中被发现。这些基因位点由短的重复DNA序列组成,这些序列之间由独特的“间隔区”序列隔开,而这些间隔区序列来源于外源遗传元件。最初被称为SRSR,其生物学功能尚不清楚,但其独特的结构表明它们在原核生物基因组中可能扮演着重要但神秘的角色。
The initial discovery of what would later be named CRISPR was an incidental finding during the sequencing of the IAP gene in Escherichia coli. Researchers led by Yoshizumi Ishino at Osaka University noticed an unusual series of 29-nucleotide repeats, partially palindromic, arranged in a cluster. These repeats were separated by non-repetitive, unique sequences of 32 nucleotides, which were later termed ‘spacers’. This peculiar structure was unlike anything previously described in bacterial genomes. At the time, DNA sequencing was a laborious process, and the function of these repeats was a complete mystery. The authors noted the structure in their publication but could not assign a biological role to it.
随后在多种其他细菌和古菌中也发现了类似的结构,表明这是原核生物基因组的普遍特征。这种结构具有一致性——重复序列和间隔序列交替出现——且重复序列在同一物种内高度保守,暗示其具有重要的功能意义。重复序列的回文性质暗示其可能形成RNA转录本中类似发夹结构的二级结构,而发夹结构是调控元件的常见特征。然而,正是间隔序列的独特性质揭示了CRISPR的功能,而这个谜题在十多年后才得以解开。这一基础性的观察性发现为后续所有关于CRISPR-Cas系统在适应性免疫中的作用及其最终在生物技术领域的应用的研究奠定了必要的基础。
CRISPR基因座
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