Van Campenhout S, Aert R, Volckaert G
Laboratory of Gene Technology, Katholieke Universiteit Leuven, Belgium.
Genome. 1998 Apr;41(2):244-55.
5S ribosomal gene spacer sequences from the short-spacer arrays of wheat and rye were isolated by PCR. The 29 new DNA sequences displayed noticeable heterogeneity at scattered positions. Nevertheless, based on shared DNA sequence polymorphisms, sequence alignment clearly classified the sequences into three groups. Group-specific primer sets were designed to allow chromosomal assignment by PCR on nullitetrasomic wheat stocks, as well as on wheat-rye translocation and addition lines. The three groups were assigned to orthologous loci 5S-Rrna-B1, 5S-Rrna-D1, and 5S-Rrna-R1 on homoeologous chromosomes 1B, 1D, and 1R, respectively. Hence, group-specific DNA sequence variation could be related to fixed orthologous DNA sequence variation between 5S rRNA multigene families on the homoeologous group 1 chromosomes. In addition, members of the three groups showed fixed orthologous length polymorphism. Four sequenced 5S-Rrna-B1 units, however, had a duplication in the gene encoding region and are probably representatives of a nontranscribed subfamily of 5S rDNA repeating units. The observed chromosome-specific polymorphisms among sequences belonging to a multigene family with thousands of copies suggests that this type of polymorphism may exist in many genes and gene families in polyploid wheats. The implication of this finding in relation to the construction of molecular tools for wheat-genome analysis and manipulation is discussed.
通过聚合酶链反应(PCR)从小麦和黑麦的短间隔序列阵列中分离出5S核糖体基因间隔序列。这29个新的DNA序列在分散位置显示出明显的异质性。然而,基于共享的DNA序列多态性,序列比对清楚地将这些序列分为三组。设计了组特异性引物对,以便通过对缺四体小麦品系以及小麦-黑麦易位系和附加系进行PCR来进行染色体定位。这三组分别被定位到同源染色体1B、1D和1R上的直系同源基因座5S-Rrna-B1、5S-Rrna-D1和5S-Rrna-R1。因此,组特异性DNA序列变异可能与同源群1染色体上5S rRNA多基因家族之间固定的直系同源DNA序列变异有关。此外,这三组的成员显示出固定的直系同源长度多态性。然而,四个测序的5S-Rrna-B1单元在基因编码区有一个重复,可能是5S rDNA重复单元的一个非转录亚家族的代表。在一个有数千个拷贝的多基因家族的序列中观察到的染色体特异性多态性表明,这种多态性可能存在于多倍体小麦的许多基因和基因家族中。讨论了这一发现对构建用于小麦基因组分析和操作的分子工具的意义。