Sequence-based functional annotation: what if most of the genes are unique to a genome?

被引:8
作者
Salavati, Reza [1 ,2 ,3 ]
Najafabadi, Hamed Shateri [1 ,2 ]
机构
[1] McGill Univ, Inst Parasitol, Montreal, PQ H9X 3V9, Canada
[2] McGill Univ, McGill Ctr Bioinformat, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
PROTEIN-PROTEIN INTERACTIONS; 3 UNTRANSLATED REGION; TRYPANOSOMATID PARASITIC PROTOZOA; MESSENGER-RNA ABUNDANCE; 3'-UNTRANSLATED REGION; DEVELOPMENTAL REGULATION; REGULATORY ELEMENT; SURFACE PROTEIN; BINDING PROTEIN; INSECT FORMS;
D O I
10.1016/j.pt.2010.02.001
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The genomes of trypanosomatids are distantly related to other eukaryotes, with significant numbers of hypothetical or conserved hypothetical trypanosomatid-specific genes, whose functions cannot be determined using homology-dependent annotation methods. Here, we describe homology-independent methods to infer biological functions of genes based solely on their sequences. These approaches are not limited to trypanosomatid genomes and provide grounds for analysis of genomes of Plasmodium falciparum and other parasites associated with neglected tropical diseases. A critical evaluation of the current state of annotation of parasitic genomes endorses the need to exploit homology-independent computational methods, which can identify protein functions, potentially including essential genes, and provide a plethora of valuable information on interaction networks and regulatory elements.
引用
收藏
页码:225 / 229
页数:5
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