Developmental regulation of gene expression in trypanosomatid parasitic protozoa

被引:155
作者
Haile, Simon [1 ,2 ]
Papadopoulou, Barbara [1 ,2 ]
机构
[1] Univ Laval, CHUQ, CHUL Res Ctr, Res Ctr Infect Dis, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Fac Med, Dept Med Biol, Quebec City, PQ G1V 4G2, Canada
关键词
D O I
10.1016/j.mib.2007.10.001
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Kinetoplastids branched early from the eukaryotic lineage and include several parasitic protozoan species. Up to several hundred kinetoplastid genes are co-transcribed into polycistronic RNAs and individual mRNAs are resolved by coupled co-transcriptional trans-splicing of a universal splice-leader RNA (SL-RNA) and T-end maturation processes. Protein-coding genes lack RNA polymerase parallel to promoters. Consequently, most of gene regulation in these organisms occurs post-transcriptionally. Over the last few years, many more genes that are regulated at the mRNA stability level and a few at the translation level have been reported. Almost all major trypanosome homologues of yeast/ mammalian mRNA degradation enzymes have been functionally characterized and major pathways identified. Novel paradigms have also recently emerged: regulated post-transcriptional processing of cytoplasmic RNAs, SL-RNA transcriptional silencing-mediated global stress response, and Leishmania-specific large-scale modulation of post-transcriptional gene expression via inactive degenerated retroelements. Several of these developments have greatly benefited from the recently completed genomic sequences and functional genomic studies.
引用
收藏
页码:569 / 577
页数:9
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