Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains: evidence for local euchromatic neighborhoods

被引:158
作者
Shopland, LS [1 ]
Johnson, CV [1 ]
Byron, M [1 ]
McNeil, J [1 ]
Lawrence, JB [1 ]
机构
[1] Univ Massachusetts, Sch Med, Med Ctr, Dept Cell Biol, Worcester, MA 01655 USA
关键词
cell nucleus; chromosome banding; genome; splicing factor SC-35; chromosome structure;
D O I
10.1083/jcb.200303131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Typically, eukaryotic nuclei contain 10-30 prominent domains (referred to here as SC-35 domains) that are concentrated in mRNA metabolic factors. Here, we show that multiple specific genes cluster around a common SC-35 domain, which contains multiple mRNAs. Nonsyntenic genes are capable of associating with a common domain, but domain "choice" appears random, even for two coordinately expressed genes. Active genes widely separated on different chromosome arms associate with the same domain frequently, assorting randomly into the 3-4 subregions of the chromosome periphery that contact a domain. Most importantly, visualization of six individual chromosome bands showed that large genomic segments (similar to5 Mb) have striking differences in organization relative to domains. Certain bands showed extensive contact, often aligning with or encircling an SC-35 domain, whereas others did not. All three gene-rich reverse bands showed this more than the gene-poor Giemsa dark bands, and morphometric analyses demonstrated statistically significant differences. Similarly, late-replicating DNA generally avoids SC-35 domains. These findings suggest a functional rationale for gene clustering in chromosomal bands, which relates to nuclear clustering of genes with SC-35 domains. Rather than random reservoirs of splicing factors, or factors accumulated on an individual highly active gene, we propose a model of SC-35 domains as functional centers for a multitude of clustered genes, forming local euchromatic "neighborhoods."
引用
收藏
页码:981 / 990
页数:10
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