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DNA PROTEASE CUTTING AGENT BASED ON CAS9 PROTEIN FROM PASTEURELLA PNEUMOTROPICA BACTERIA

机译:拟南芥芽孢杆菌CAS9蛋白切割DNA蛋白酶的研究

摘要

FIELD: biotechnology.;SUBSTANCE: invention relates to the biotechnology. Described is the use of a protein capable of forming a double-strand break in a DNA sequence directly adjacent to sequence 5'-NNNN(A/G)T-3' containing the amino acid sequence SEQ ID NO: 1 or containing amino acid sequence, which is at least 95 % identical to the amino acid sequence SEQ ID NO: 1 and has differences compared to SEQ ID NO: 1 only in non-conservative amino acid residues, to form double-strand break in DNA molecule located immediately before nucleotide sequence 5'-NNNN(A/G)T-3' in said DNA molecule. In addition, described is a method of forming a double-strand break in a sequence of genomic DNA of a unicellular or multicellular organism directly adjacent to sequence 5'-NNNN(A/G)T-3'. Introducing at least one cell of said organism an effective amount of a) a protein comprising the amino acid sequence SEQ ID NO: 1 and capable of forming a double-strand break in the DNA sequence directly adjacent to sequence 5'-NNNN(A/G)T-3', or nucleic acid coding said protein, and b) a RNA guide containing a duplex-forming sequence with a nucleotide sequence of a genomic DNA portion of the organism immediately adjacent to nucleotide sequence 5'-NNNN(A/G)T-3', and interacts with said protein after formation of duplex, or DNA sequence coding said RNA guide. Interaction of said protein with the RNA guide and 5'-NNNN(A/G)T-3' nucleotide sequence leads to formation of double-strand break in a sequence of genomic DNA directly adjacent to sequence 5'-NNNN(A/G)T-3'.;EFFECT: thereby achieving higher universality of available CRISPR-Cas9 systems, which will make it possible to use Cas9 nucleases from different organisms for cutting genome or plasmid DNA in more specific sites and under different conditions.;5 cl, 13 dwg, 2 tbl, 4 ex
机译:技术领域本发明涉及生物技术。描述了一种蛋白质的用途,该蛋白质能够在与包含氨基酸序列SEQ ID NO:1或包含氨基酸的序列5'-NNNN(A / G)T-3'直接相邻的DNA序列中形成双链断裂该序列与SEQ ID NO:1的氨基酸序列至少有95%的同一性,并且仅在非保守氨基酸残基上与SEQ ID NO:1相比具有差异,从而在紧接之前的DNA分子中形成双链断裂所述DNA分子中的核苷酸序列5'-NNNN(A / G)T-3'。另外,描述了一种在与序列5'-NNNN(A / G)T-3'直接相邻的单细胞或多细胞生物的基因组DNA的序列中形成双链断裂的方法。向所述生物的至少一个细胞中引入有效量的a)包含氨基酸序列SEQ ID NO:1并能够在与序列5'-NNNN(A / G)T-3'或编码所述蛋白质的核酸,和b)RNA向导,其中包含双链体形成序列,该双链体形成序列的生物体基因组DNA部分的核苷酸序列紧邻核苷酸序列5'-NNNN(A / G)T-3',并在形成双链体或编码所述RNA向导的DNA序列后与所述蛋白质相互作用。所述蛋白质与RNA向导和5'-NNNN(A / G)T-3'核苷酸序列的相互作用导致在与序列5'-NNNN(A / G)直接相邻的基因组DNA序列中形成双链断裂)T-3';作用:从而实现可用的CRISPR-Cas9系统的更高通用性,这将使得有可能使用来自不同生物的Cas9核酸酶在更特定的位点和不同的条件下切割基因组或质粒DNA; 5 ,13载重吨,2汤匙,4前

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