Genomic and proteomic evidence for a second family of dense core granule cargo proteins in Tetrahymena thermophila

被引:25
作者
Bowman, GR
Smith, DGS
Siu, KWM
Pearlman, RE
Turkewitz, AP [1 ]
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[2] York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada
[3] York Univ, Ctr Res Mass Spect, Toronto, ON M3J 1P3, Canada
[4] York Univ, Dept Biol, Toronto, ON M3J 1P3, Canada
关键词
ciliate; beta/gamma-crystallin; exocytosis; gene duplication;
D O I
10.1111/j.1550-7408.2005.00045.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In addition to a family of structurally related proteins encoded by the Granule lattice (GRL) genes, the dense core granules in Tetrahymena thermophilo contain a second, more heterogeneous family of proteins that can be defined by the presence of a domain homologous to beta/gamma-crystallins. The founding members of the family, Induced during Granule Regeneration 1 (IGR1) and Granule Tip 1 (GRT1), were identified in previous screens for granule components. Analysis of the recently sequenced T. thermophila macronuclear genome has now uncovered 11 additional related genes. All family members have a single beta/gamma-crystallin domain, but the overall predicted organization of family members is highly variable, and includes three other motif's that are conserved between subsets of family members. To demonstrate that these proteins are present within granules, polypeptides from a subcellular fraction enriched in granules were analyzed by mass spectrometry. This positively identified four of the predicted novel beta/gamma-crystallin domain proteins. Both the functional evidence for IGR1 and GRT1 and the variability in the overall structure of this new protein family suggest that its members play roles that are distinct from those of the GRL family.
引用
收藏
页码:291 / 297
页数:7
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