Widespread variation in transcript abundance within and across developmental stages of Trypanosoma brucei

被引:113
作者
Jensen, Bryan C. [1 ]
Sivam, Dhileep [1 ,2 ]
Kifer, Charles T. [1 ]
Myler, Peter J. [1 ,2 ,3 ]
Parsons, Marilyn [1 ,3 ]
机构
[1] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[2] Univ Washington, Dept Med Educ & Biomed Informat, Seattle, WA 98195 USA
[3] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
关键词
BLOOD-STREAM FORMS; DIFFERENTIAL GENE-EXPRESSION; LIFE-CYCLE STAGES; LEISHMANIA-MAJOR; POLYCISTRONIC TRANSCRIPTION; AFRICAN TRYPANOSOMES; BINDING PROTEIN; MESSENGER-RNAS; DNA-MICROARRAY; METABOLISM;
D O I
10.1186/1471-2164-10-482
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Trypanosoma brucei, the causative agent of African sleeping sickness, undergoes a complex developmental cycle that takes place in mammalian and insect hosts and is accompanied by changes in metabolism and cellular morphology. While differences in mRNA expression have been described for many genes, genome-wide expression analyses have been largely lacking. Trypanosomatids represent a unique case in eukaryotes in that they transcribe protein-coding genes as large polycistronic units, and rarely regulate gene expression at the level of transcription initiation. Results: Here we present a comprehensive analysis of mRNA expression in several stages of parasite development. Utilizing microarrays that have multiple copies of multiple probes for each gene, we were able to demonstrate with a high degree of statistical confidence that approximately one-fourth of genes show differences in mRNA expression levels in the stages examined. These include complex patterns of gene expression within gene families, including the large family of variant surface glycoproteins (VSGs) and their relatives, where we have identified a number of constitutively expressed family members. Furthermore, we were able to assess the relative abundance of all transcripts in each stage, identifying the genes that are either weakly or highly expressed. Very few genes show no evidence of expression. Conclusion: Despite the lack of gene regulation at the level of transcription initiation, our results reveal extensive regulation of mRNA abundance associated with different life cycle and growth stages. In addition, analysis of variant surface glycoprotein gene expression reveals a more complex picture than previously thought. These data provide a valuable resource to the community of researchers studying this lethal agent.
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页数:24
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