animal hect ubiquitin ligases evolution and functional implications动物hect泛素连接酶进化和功能的影响.pdfVIP
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animal hect ubiquitin ligases evolution and functional implications动物hect泛素连接酶进化和功能的影响
Marín BMC Evolutionary Biology 2010, 10:56
/1471-2148/10/56
RESEARCH ARTICLE Open Access
Animal HECT ubiquitin ligases: evolution and
functional implications
*
Ignacio Marín
Abstract
Background: HECT ubiquitin ligases (HECT E3s) are key components of the eukaryotic ubiquitin-proteasome
system and are involved in the genesis of several human diseases. In this study, I analyze the patterns of
diversification of HECT E3s since animals emerged in order to provide the right framework to understand the
functional data available for proteins of this family.
Results: I show that the current classification of HECT E3s into three groups (NEDD4-like E3s, HERCs and single-
HECT E3s) is fundamentally incorrect. First, the existence of a “Single-HECT E3s” group is not supported by
phylogenetic analyses. Second, the HERC proteins must be divided into two subfamilies (Large HERCs, Small HERCs)
that are evolutionarily very distant, their structural similarity being due to convergence and not to a common
origin. Sequence and structural analyses show that animal HECT E3s can be naturally classified into 16 subfamilies.
Almost all of them appeared either before animals originated or in early animal evolution. More recently, multiple
gene losses have occurred independently in some lineages (nematodes, insects, urochordates), the same groups
that have also lost genes of another type of E3s (RBR family). Interestingly, the emergence of some animal HECT
E3s precedes the origin of key cellular systems that they regulate (TGF-b and EGF signal transduction pathways;
p53 family of transcription factors) and it can be deduced that distantly related HECT proteins have been
independently co-opted to perform similar roles. This may contribute to explain why distantly related HECT E3s are
involved in the genesis of multiple
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