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本文引用的文献

1
Efficient random subcloning of DNA sheared in a recirculating point-sink flow system.在循环点-汇流系统中对剪切后的DNA进行高效随机亚克隆。
Nucleic Acids Res. 1996 Oct 15;24(20):3879-86. doi: 10.1093/nar/24.20.3879.
2
Random subcloning of sonicated DNA: application to shotgun DNA sequence analysis.经超声处理的DNA的随机亚克隆:在鸟枪法DNA序列分析中的应用
Anal Biochem. 1983 Feb 15;129(1):216-23. doi: 10.1016/0003-2697(83)90072-6.
3
Shotgun DNA sequencing using cloned DNase I-generated fragments.使用克隆的脱氧核糖核酸酶I产生的片段进行鸟枪法DNA测序。
Nucleic Acids Res. 1981 Jul 10;9(13):3015-27. doi: 10.1093/nar/9.13.3015.
4
Improved tools for biological sequence comparison.用于生物序列比较的改进工具。
Proc Natl Acad Sci U S A. 1988 Apr;85(8):2444-8. doi: 10.1073/pnas.85.8.2444.

一种用于可控、无偏倚DNA剪切的自动化流体动力学方法。

An automated hydrodynamic process for controlled, unbiased DNA shearing.

作者信息

Thorstenson Y R, Hunicke-Smith S P, Oefner P J, Davis R W

机构信息

Stanford DNA Sequencing and Technology Center, Palo Alto, California 94304, USA.

出版信息

Genome Res. 1998 Aug;8(8):848-55. doi: 10.1101/gr.8.8.848.

DOI:10.1101/gr.8.8.848
PMID:9724331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC310760/
Abstract

An automated, inexpensive, easy-to-use, and reproducible technique for controlled, random DNA fragmentation has been developed. The technique is based on point-sink hydrodynamics that result when a DNA sample is forced through a small hole by a syringe pump. Commercially available components are used to reduce the cost and complexity of the instrument. The design is optimized to reduce the volume of sample required and to speed processing time. Shearing of the samples can be completely automated by computer control. Ninety percent of sheared DNA fragments fall within a twofold size distribution that is highly reproducible. Three parameters are critical: the flow geometry, the flow rate, and a minimum number of iterations. Shearing is reproducible over a wide range of temperatures, DNA concentrations, and initial DNA size. The cloning efficiency of the sheared DNA is very good even without end repair, the distribution of assembled sequences is random, and there is no sequence bias at the ends of sheared fragments that have been cloned. The instrument, called the Point-sink Shearer (PtS), has already been exported successfully to many other laboratories.

摘要

已开发出一种用于可控、随机DNA片段化的自动化、低成本、易于使用且可重复的技术。该技术基于点-汇流体动力学,当DNA样品通过注射泵被压过一个小孔时会产生这种现象。使用市售组件来降低仪器的成本和复杂性。该设计经过优化,以减少所需样品的体积并加快处理时间。样品的剪切可通过计算机控制完全自动化。90%的剪切DNA片段落在高度可重复的两倍大小分布范围内。三个参数至关重要:流动几何形状、流速和最小迭代次数。在很宽的温度、DNA浓度和初始DNA大小范围内,剪切都是可重复的。即使不进行末端修复,剪切DNA的克隆效率也非常好,组装序列的分布是随机的,并且在已克隆的剪切片段末端没有序列偏差。该仪器称为点-汇剪切仪(PtS),已经成功出口到许多其他实验室。