Literature DB >> 16807745

Expansion of the mast cell chymase locus over the past 200 million years of mammalian evolution.

Maike Gallwitz1, Jenny M Reimer, Lars Hellman.   

Abstract

The acidic granules of natural killer (NK) cells, T cells, mast cells, and neutrophils store large amounts of serine proteases. Functionally, these proteases are involved, e.g., in the induction of apoptosis, the recruitment of inflammatory cells, and the remodeling of extra-cellular matrix. Among the granule proteases are the phylogenetically related mast cell chymases, neutrophil cathepsin G, and T-cell granzymes (Gzm B to H and Gzm N), which share the characteristic absence of a Cys(191)-Cys(220) bridge. The genes of these proteases are clustered in one locus, the mast cell chymase locus, in all previously investigated mammals. In this paper, we present a detailed analysis of the chymase locus in cattle (Bos taurus) and opossum (Monodelphis domestica). The gained information delineates the evolution of the chymase locus over more than 200 million years. Surprisingly, the cattle chymase locus contains two alpha-chymase and two cathepsin G genes where all other studied chymase loci have single genes. Moreover, the cattle locus holds at least four genes for duodenases, which are not found in other chymase loci. Interestingly, duodenases seem to have digestive rather than immune functions. In opossum, on the other hand, only two chymase locus-related genes have been identified. These two genes are not arranged in one locus, but appear to have been separated by a marsupial-specific chromosomal rearrangement. Phylogenetic analyses place one of the opossum genes firmly with mast cell alpha-chymases, which indicates that the alpha-chymase had already evolved as a separate, clearly identifiable gene before the separation of marsupials and placental mammals. In contrast, the second gene in opossum is positioned phylogenetically between granzymes, cathepsin G, and the duodenases. These genes, therefore, probably evolved as separate subfamilies after the separation of placental mammals from marsupials. In platypus, only one chymase locus-like sequence could be identified. This previously published "granzyme" does not cluster clearly with any of the chymase locus gene families, but shares the absence of the Cys(191)-Cys(220) bridge with the other chymase locus proteases. These findings indicate that all chymase locus genes are derived from a single ancestor that was present more than 200 million years ago.

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Year:  2006        PMID: 16807745     DOI: 10.1007/s00251-006-0126-1

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  51 in total

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3.  Sheep mast cell proteinase-1: characterization as a member of a new class of dual-specific ruminant chymases.

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Authors:  G H Caughey; W W Raymond; P J Wolters
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Authors:  V Z Pletnev; T S Zamolodchikova; W A Pangborn; W L Duax
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8.  Rodent alpha-chymases are elastase-like proteases.

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9.  Specificity of human cathepsin G.

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10.  The chymase, mouse mast cell protease 4, constitutes the major chymotrypsin-like activity in peritoneum and ear tissue. A role for mouse mast cell protease 4 in thrombin regulation and fibronectin turnover.

Authors:  Elena Tchougounova; Gunnar Pejler; Magnus Abrink
Journal:  J Exp Med       Date:  2003-08-04       Impact factor: 14.307

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  26 in total

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Review 2.  Mast cell tryptases and chymases in inflammation and host defense.

Authors:  George H Caughey
Journal:  Immunol Rev       Date:  2007-06       Impact factor: 12.988

Review 3.  Mast cell peptidases: chameleons of innate immunity and host defense.

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Review 4.  Mast cell proteases as pharmacological targets.

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Review 5.  Potential effector and immunoregulatory functions of mast cells in mucosal immunity.

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Review 6.  Protective and pathological roles of mast cells and basophils.

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8.  High degree of conservation of the multigene tryptase locus over the past 150-200 million years of mammalian evolution.

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Journal:  Immunogenetics       Date:  2010-04-10       Impact factor: 2.846

9.  Guinea pig chymase is leucine-specific: a novel example of functional plasticity in the chymase/granzyme family of serine peptidases.

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10.  Mast cell alpha and beta tryptases changed rapidly during primate speciation and evolved from gamma-like transmembrane peptidases in ancestral vertebrates.

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Journal:  J Immunol       Date:  2007-11-01       Impact factor: 5.422

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