Noël T, Labarère J
Laboratoire de Génétique Moléculaire et Amélioration des Champignons Cultivés, Université de Bordeaux II-INRA, Villenave d'Ornon, France.
Curr Genet. 1994 May;25(5):432-7. doi: 10.1007/BF00351782.
The URA1 gene, encoding dihydroorotate dehydrogenase of the pyrimidine pathway, cloned into pUC18 (pUra1-1) was used to develop an homologous transformation system for the cultivated mushroom Agrocybe aegerita. Protoplasts of a ura1 auxotrophic strain were transformed by electroporation with efficiencies ranging from 1 to 26 transformants per micrograms of DNA. The phenotype of the stable Ura+ transformants suggested a strong nuclear heterogeneity further confirmed by Southern-blot analysis. All transformants acquired extrachromosomal forms derived from pUra1-1. Integration of pUra1-1 into chromosomal DNA occurred for some transformants. Plasmids containing the integrant of pUC18 recombined to different parts of the URA1 gene were rescued from A. aegerita transformants through transformation of E. coli. Their molecular analysis indicated that they represent products of the continuous excision of primary-integrated vector sequences rather than ARS-dependent autoreplicative forms.
URA1基因编码嘧啶途径中的二氢乳清酸脱氢酶,将其克隆到pUC18中(pUra1 - 1),用于构建栽培蘑菇柱状田头菇的同源转化系统。ura1营养缺陷型菌株的原生质体通过电穿孔转化,转化效率为每微克DNA产生1至26个转化体。稳定的Ura +转化体的表型表明存在强烈的核异质性,Southern杂交分析进一步证实了这一点。所有转化体都获得了源自pUra1 - 1的染色体外形式。一些转化体中发生了pUra1 - 1整合到染色体DNA中。通过大肠杆菌转化,从柱状田头菇转化体中拯救出含有重组到URA1基因不同部位的pUC18整合体的质粒。它们的分子分析表明,它们代表初级整合载体序列连续切除的产物,而不是依赖于自主复制序列(ARS)的自主复制形式。