Institute of Natural Sciences, Massey University, Auckland, New Zealand.
PLoS One. 2011;6(12):e29267. doi: 10.1371/journal.pone.0029267. Epub 2011 Dec 19.
The three-dimensional organization of genomes is dynamic and plays a critical role in the regulation of cellular development and phenotypes. Here we use proximity-based ligation methods (i.e. chromosome conformation capture [3C] and circularized chromosome confrmation capture [4C]) to explore the spatial organization of tRNA genes and their locus-specific interactions with the ribosomal DNA. Directed replacement of one lysine and two leucine tRNA loci shows that tRNA spatial organization depends on both tRNA coding sequence identity and the surrounding chromosomal loci. These observations support a model whereby the three-dimensional, spatial organization of tRNA loci within the nucleus utilizes tRNA gene-specific signals to affect local interactions, though broader organization of chromosomal regions are determined by factors outside the tRNA genes themselves.
基因组的三维组织是动态的,在细胞发育和表型的调控中起着关键作用。在这里,我们使用基于邻近性的连接方法(即染色体构象捕获[3C]和环形染色体构象捕获[4C])来探索 tRNA 基因的空间组织及其与核糖体 DNA 的位置特异性相互作用。靶向替换一个赖氨酸和两个亮氨酸 tRNA 基因座表明,tRNA 的空间组织既取决于 tRNA 编码序列的同一性,也取决于周围的染色体基因座。这些观察结果支持了这样一种模型,即核内 tRNA 基因座的三维空间组织利用 tRNA 基因特异性信号来影响局部相互作用,尽管染色体区域的更广泛组织是由 tRNA 基因本身之外的因素决定的。