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Biased assembly of the nuclear pore complex is required for somatic and germline nuclear differentiation in Tetrahymena
Author(s) -
Masaaki Iwamoto,
Takako Koujin,
Hiroko Osakada,
Chie Mori,
Tomoko Kojidani,
Atsushi Matsuda,
Haruhiko Asakawa,
Yasushi Hiraoka,
Tokuko Haraguchi
Publication year - 2015
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.167353
Subject(s) - macronucleus , biology , nuclear pore , tetrahymena , microbiology and biotechnology , somatic cell , ciliate , germline , mitosis , cell division , inner membrane , cell nucleus , nucleoporin , genetics , nucleus , nuclear transport , cell , gene , mitochondrion
Ciliates have two functionally distinct nuclei, a somatic macronucleus (MAC) and a germline micronucleus (MIC) that develop from daughter nuclei of the last postzygotic division (PZD) during the sexual process of conjugation. Understanding this nuclear dimorphism is a central issue in ciliate biology. We show, by live-cell imaging of Tetrahymena, that biased assembly of the nuclear pore complex (NPC) occurs immediately after the last PZD, which generates anterior-posterior polarized nuclei: MAC-specific NPCs assemble in anterior presumptive MACs but not in posterior presumptive MICs. MAC-specific NPC assembly in the anterior nuclei occurs much earlier than transport of Twi1p, which is required for MAC genome rearrangement. Correlative light-electron microscopy shows that addition of new nuclear envelope (NE) precursors occurs through the formation of domains of redundant NE, where the outer double membrane contains the newly assembled NPCs. Nocodazole inhibition of the second PZD results in assembly of MAC-specific NPCs in the division-failed zygotic nuclei, leading to failure of MIC differentiation. Our findings demonstrate that NPC type switching has a crucial role in the establishment of nuclear differentiation in ciliates.

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