1.Emerging genomic and proteomic evidence on relationships among the animal, plant and fungal kingdoms.
Genomics, Proteomics & Bioinformatics 2004;2(2):70-76
Sequence-based molecular phylogenies have provided new models of early eukaryotic evolution. This includes the widely accepted hypothesis that animals are related most closely to fungi, and that the two should be grouped together as the Opisthokonta. Although most published phylogenies have supported an opisthokont relationship, a number of genes contain a tree-building signal that clusters animal and green plant sequences, to the exclusion of fungi. The alternative tree-building signal is especially intriguing in light of emerging data from genomic and proteomic studies that indicate striking and potentially synapomorphic similarities between plants and animals. This paper reviews these new lines of evidence, which have yet to be incorporated into models of broad scale eukaryotic evolution.
Animals
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Biological Evolution
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Cell Differentiation
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physiology
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Fungi
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cytology
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genetics
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Genomics
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Humans
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Phylogeny
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Plant Cells
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Plants
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genetics
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Proteomics
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RNA Caps
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biosynthesis
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RNA, Messenger
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metabolism
2.hNUDT16: a universal decapping enzyme for small nucleolar RNA and cytoplasmic mRNA.
Guangwen LU ; Jie ZHANG ; Yan LI ; Zhixin LI ; Na ZHANG ; Xiang XU ; Tingting WANG ; Zhenhong GUAN ; George F GAO ; Jinghua YAN
Protein & Cell 2011;2(1):64-73
Human NUDT16 (hNUDT16) is a decapping enzyme initially identified as the human homolog to the Xenopus laevis X29. As a metalloenzyme, hNUDT16 relies on divalent cations for its cap-hydrolysis activity to remove m⁷GDP and m²²⁷GDP from RNAs. Metal also determines substrate specificity of the enzyme. So far, only U8 small nucleolar RNA (snoRNA) has been identified as the substrate of hNUDT16 in the presence of Mg²(+). Here we demonstrate that besides U8, hNUDT16 can also actively cleave the m⁷GDP cap from mRNAs in the presence of Mg²(+) or Mn²(+). We further show that hNUDT16 does not preferentially recognize U8 or mRNA substrates by our cross-inhibition and quantitative decapping assays. In addition, our mutagenesis analysis identifies several key residues involved in hydrolysis and confirms the key role of the REXXEE motif in catalysis. Finally an investigation into the subcellular localization of hNUDT16 revealed its abundance in both cytoplasm and nucleus. These findings extend the substrate spectrum of hNUDT16 beyond snoRNAs to also include mRNA, demonstrating the pleiotropic decapping activity of hNUDT16.
Amino Acid Motifs
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Biocatalysis
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Cell Nucleus
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enzymology
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Consensus Sequence
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Cytoplasm
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enzymology
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metabolism
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Guanosine Diphosphate
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metabolism
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Histidine
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metabolism
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Humans
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Hydrolysis
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Luciferases
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genetics
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Magnesium
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metabolism
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Manganese
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metabolism
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Mutagenesis
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Mutation
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Pyrophosphatases
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antagonists & inhibitors
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chemistry
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genetics
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metabolism
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RNA Caps
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chemistry
;
metabolism
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pharmacology
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RNA, Small Nucleolar
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chemistry
;
metabolism
;
pharmacology