Hou G, Le Blancq S M, E Y, Zhu H, Lee M G
Department of Pathology, New York University Medical Center, NY 10016, USA.
Nucleic Acids Res. 1995 Aug 25;23(16):3310-7. doi: 10.1093/nar/23.16.3310.
It has been shown previously that the rRNA encoding chromosomes in Giardia lamblia undergo frequent rearrangements with an estimated rate of approximately 1% per cell per division (Le Blancq et al., 1992, Nucleic Acids Res., 17, 4539-4545). Following these observations, we searched for highly recombinogenic regions in one of the frequently rearranged rRNA encoding chromosomes, that is chromosome 1, a small, 1.1 Mb chromosome. Chromosome 1 undergoes frequent rearrangements that result in size variation of 5-20%. We analyzed the structure of chromosome 1 in clonal lineages from the WB strain. The two ends of chromosome 1 comprise telomere repeat [TAGGG] arrays joined to a truncated rRNA gene and a sequence referred to as '4e', respectively. Comparison of the structure of four polymorphic versions of chromosome 1, resulting from independent rearrangement events in four cloned lines, located a single polymorphic region to the variable rDNA-telomere domain. Chromosome 1 is organized into two domains: a core region spanning approximately 850 kb that does not exhibit size heterogeneity among different chromosome 1 and a variable region that spans 185-450 kb and includes the telomeric rRNA genes, referred to as the variable rDNA-telomere domain. The core region contains a conserved region, spanning approximately 550 kb adjacent to the telomeric 4e sequence, which is only present in the 4e containing chromosomes and a 300 kb region of repetitive sequences that are also components of other chromosomes as well. Changes in the number of rDNA repeats accounted for some, but not all, of the size variation. Since there are four chromosomes that share the core region of chromosome 1, we suggest that the genome is tetraploid for this chromosome.
先前的研究表明,蓝氏贾第鞭毛虫中编码核糖体RNA(rRNA)的染色体频繁发生重排,估计每个细胞每次分裂的重排率约为1%(Le Blancq等人,1992年,《核酸研究》,17卷,4539 - 4545页)。基于这些观察结果,我们在其中一条频繁重排的rRNA编码染色体(即1号染色体,一条小的1.1兆碱基对染色体)中寻找高度重组区域。1号染色体频繁发生重排,导致大小变化5% - 20%。我们分析了WB株系克隆谱系中1号染色体的结构。1号染色体的两端分别由端粒重复序列[TAGGG]阵列连接到一个截短的rRNA基因和一个称为“4e”的序列组成。对四个克隆系中独立重排事件产生的1号染色体的四个多态性版本的结构进行比较,将一个单一的多态性区域定位到可变的核糖体DNA - 端粒结构域。1号染色体被组织成两个结构域:一个核心区域,跨度约850千碱基对,在不同的1号染色体之间不表现出大小异质性;一个可变区域,跨度为185 - 450千碱基对,包括端粒rRNA基因,称为可变核糖体DNA - 端粒结构域。核心区域包含一个保守区域,跨度约550千碱基对,与端粒4e序列相邻,仅存在于含有4e的染色体中,还有一个300千碱基对的重复序列区域,也是其他染色体的组成部分。核糖体DNA重复序列数量的变化部分(但不是全部)解释了大小变异。由于有四条染色体共享1号染色体的核心区域,我们认为该染色体的基因组是四倍体。