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The nuclear pore complex (NPC) has dual roles in nucleocytoplasmic transport and chromatin organization. In many eukaryotes the coiled-coil Mlp/Tpr proteins of the NPC nuclear basket have specific functions in interactions with chromatin and defining specialized regions of active transcription, whereas Mlp2 associates with the mitotic spindle/NPC in a cell cycle-dependent manner. We previously identified two putative Mlp-related proteins in African trypanosomes, TbNup110 and TbNup92, the latter of which associates with the spindle. We now provide evidence for independent ancestry for TbNup92/TbNup110 and Mlp/Tpr proteins. However, TbNup92 is required for correct chromosome segregation, with knockout cells exhibiting microaneuploidy and lowered fidelity of telomere segregation. Further, TbNup92 is intimately associated with the mitotic spindle and spindle anchor site but apparently has minimal roles in control of gene transcription, indicating that TbNup92 lacks major barrier activity. TbNup92 therefore acts as a functional analogue of Mlp/Tpr proteins, and, together with the lamina analogue NUP-1, represents a cohort of novel proteins operating at the nuclear periphery of trypanosomes, uncovering complex evolutionary trajectories for the NPC and nuclear lamina.

Original publication

DOI

10.1091/mbc.E13-12-0750

Type

Journal article

Journal

Mol Biol Cell

Publication Date

05/2014

Volume

25

Pages

1421 - 1436

Keywords

Cell Nucleus, Chromosome Segregation, Evolution, Molecular, G2 Phase Cell Cycle Checkpoints, Mitosis, Nuclear Pore, Nuclear Pore Complex Proteins, Phylogeny, Protein Structure, Secondary, Protein Structure, Tertiary, Protein Transport, Protozoan Proteins, Transcription, Genetic, Trypanosoma brucei brucei