Verdoes J C, Calil M R, Punt P J, Debets F, Swart K, Stouthamer A H, van den Hondel C A
Department of Molecular Genetics and Gene Technology, TNO Nutrition and Food Research Institute, Rijswijk, The Netherlands.
Mol Gen Genet. 1994 Jul 8;244(1):75-80. doi: 10.1007/BF00280189.
A method is described for unambiguous assignment of cloned genes to Aspergillus niger chromosomes by CHEF gel electrophoresis and Southern analysis. All of the eight linkage groups (LGs), with the exception of LG VII, have previously been assigned to specific chromosomal bands in the electrophoretic karyotype of A. niger. Using a LG VII-specific probe (nicB gene of A. niger) we have shown that LG VII corresponds to a chromosome of about 4.1 Mb. Furthermore, genetic localization of three unassigned genes (glaA, aglA and pepA) in strains in which these genes had been replaced by a selectable marker gene led to a revised karyotype for the chromosomes corresponding to LGs VIII and VI. The revised electrophoretic karyotype reveals only 5 distinct bands. The presence of three pairs of equally sized chromosomes precluded assignment of genes to one specific chromosome in the wild-type strain. However, unambiguous chromosome assignment of cloned genes using CHEF-Southern analysis was demonstrated using a set of A. niger strains with introduced chromosomal size variation. The availability of these tester strains obviates the need to isolate or construct mutant strains for the purpose of chromosome assignment.
描述了一种通过脉冲场凝胶电泳(CHEF)和Southern分析将克隆基因明确分配到黑曲霉染色体上的方法。除了连锁群VII(LG VII)外,之前已将所有八个连锁群(LGs)分配到黑曲霉电泳核型中的特定染色体条带。使用LG VII特异性探针(黑曲霉的nicB基因),我们已表明LG VII对应于一条约4.1 Mb的染色体。此外,在这些基因已被选择标记基因取代的菌株中对三个未分配基因(glaA、aglA和pepA)进行遗传定位,导致对应于LGs VIII和VI的染色体的核型发生了修订。修订后的电泳核型仅显示5个不同的条带。三对大小相等的染色体的存在使得无法在野生型菌株中将基因分配到一条特定的染色体上。然而,使用一组具有引入的染色体大小变异的黑曲霉菌株,通过CHEF-Southern分析证明了克隆基因的明确染色体分配。这些测试菌株的可用性消除了为染色体分配目的而分离或构建突变菌株的需要。