Tseng Hung, Chou Weichin, Wang Junwen, Zhang Xiaohong, Zhang Shengliang, Schultz Richard M
Department of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2008 Mar 26;3(3):e1843. doi: 10.1371/journal.pone.0001843.
Previous cytogenetic studies suggest that various rDNA chromosomal loci are not equally active in different cell types. Consistent with this variability, rDNA polymorphism is well documented in human and mouse. However, attempts to identify molecularly rDNA variant types, which are regulated individually (i.e., independent of other rDNA variants) and tissue-specifically, have not been successful. We report here the molecular cloning and characterization of seven mouse rDNA variants (v-rDNA). The identification of these v-rDNAs was based on restriction fragment length polymorphisms (RFLPs), which are conserved among individuals and mouse strains. The total copy number of the identified variants is less than 100 and the copy number of each individual variant ranges from 4 to 15. Sequence analysis of the cloned v-rDNA identified variant-specific single nucleotide polymorphisms (SNPs) in the transcribed region. These SNPs were used to develop a set of variant-specific PCR assays, which permitted analysis of the v-rDNAs' expression profiles in various tissues. These profiles show that three v-rDNAs are expressed in all tissues (constitutively active), two are expressed in some tissues (selectively active), and two are not expressed (silent). These expression profiles were observed in six individuals from three mouse strains, suggesting the pattern is not randomly determined. Thus, the mouse rDNA array likely consists of genetically distinct variants, and some are regulated tissue-specifically. Our results provide the first molecular evidence for cell-type-specific regulation of a subset of rDNA.
以往的细胞遗传学研究表明,各种核糖体DNA(rDNA)染色体位点在不同细胞类型中的活性并不相同。与这种变异性一致,rDNA多态性在人类和小鼠中已有充分记录。然而,试图从分子水平上鉴定受单独调控(即独立于其他rDNA变体)且具有组织特异性的rDNA变体类型的尝试尚未成功。我们在此报告了7种小鼠rDNA变体(v-rDNA)的分子克隆和特性分析。这些v-rDNA的鉴定基于限制性片段长度多态性(RFLP),其在个体和小鼠品系中是保守的。所鉴定变体的总拷贝数少于100个,每个个体变体的拷贝数在4到15个之间。对克隆的v-rDNA进行序列分析,在转录区域鉴定出了变体特异性单核苷酸多态性(SNP)。这些SNP被用于开发一组变体特异性PCR检测方法,从而能够分析v-rDNA在各种组织中的表达谱。这些表达谱显示,三种v-rDNA在所有组织中均有表达(组成型活性),两种在某些组织中有表达(选择性活性),两种不表达(沉默)。在来自三个小鼠品系的六个个体中均观察到了这些表达谱,表明这种模式并非随机决定。因此,小鼠rDNA阵列可能由遗传上不同的变体组成,并且其中一些受到组织特异性调控。我们的结果为rDNA的一个子集的细胞类型特异性调控提供了首个分子证据。