ku70基因敲除对疣状青霉菌丝真菌转化频率的影响

Igor G. Sinelnikov, Valeriy Yu. Kislitsin, Andrey M. Chulkin, Andrey A. Shaplin, Aleksandra M. Rozhkova
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引用次数: 0

摘要

为了提高工业菌株疣状Penicillium verruculosum 221-151 (VKM F-3972D)转化过程中同源重组(homologous recombination, HR)的频率,利用CRISPR/CAS9方法敲除编码ku70的基因,该基因结合于双链DNA断裂位点,通过非同源末端关节(non-homologous end joint, NHEJ)参与修复过程。据推测,新宿主菌株P. verruculosum ΔniaDΔku70在转化过程中与宿主菌株P. verruculosum ΔniaD相比,同源重组的频率应该有所增加,这是由于表达盒仅通过HR机制整合插入。选择编码同源天冬氨酸蛋白酶的pep1基因作为标记。然而,研究表明,在相同的外源DNA负荷(3 μg)下,敲除ku70基因导致疣状假单胞菌ΔniaDΔku70菌株的共转化频率明显低于疣状假单胞菌ΔniaD菌株。疣状假单胞菌pep1(原生库70)序列重组菌株的pep1基因拷贝数在3 ~ 28个拷贝之间,表明非同源重组机制占主导地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
INFLUENCE OF KU70 GENE KNOCKOUT ON TRANSFORMATION FREQUENCY OF PENICILLIUM VERRUCULOSUM MYCELIAL FUNGI
To increase the frequency of homologous recombination (HR) during the transformation of the industrial strain Penicillium verruculosum 221-151 (VKM F-3972D), the ku70 gene encoding the Ku70, which binds at the sites of double-stranded DNA breaks and is involved in the repair process by the non-homologous end joint (NHEJ), was knocked out by the CRISPR/CAS9 method. Presumably, the new host strain, P. verruculosum ΔniaDΔku70, should have had an increased frequency of homologous recombination during transformation in comparison with the host strain P. verruculosum ΔniaD due to the integrative insertion of the expression cassette only by the HR mechanism. The pep1 gene encoding homologous aspartate protease was chosen as a marker. However, it was shown that the knockout of the ku70 gene led to a dramatic decrease in the frequency of co-transformation in the P. verruculosum ΔniaDΔku70 strain compared to the P. verruculosum ΔniaD strain at the same load of exogenous DNA (3 μg). The number of copies of the pep1 gene in recombinant strains of the P. verruculosum Pep1 (with a native Ku70) series ranged from 3 to 28 copies, which indicated the predominance of the non-homologous recombination mechanism.
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