Abstract
γ-Tubulin regulates the nucleation of microtubules, but knowledge of its functions in vivo is still fragmentary. Here, we report the identification of two closely related γ-tubulin isoforms, TUBG1 and TUBG2, in mice, and the generation of TUBG1- and TUBG2-deficient mice. TUBG1 was expressed ubiquitously, whereas TUBG2 was primarily detected in the brain. The development of TUBG1-deficient (Tubg1-/-) embryos stopped at the morula/blastocyst stages due to a characteristic mitotic arrest: the mitotic spindle was highly disorganized, and disorganized spindles showed one or two pole-like foci of bundled MTs that were surrounded by condensed chromosomes. TUBG2 was expressed in blastocysts, but could not rescue the TUBG1 deficiency. By contrast, TUBG2-deficient (Tubg2-/-) mice were born, grew, and intercrossed normally. In the brain of wild-type mice, TUBG2 was expressed in approximately the same amount as TUBG1, but no histological abnormalities were found in the Tubg2-/- brain. These findings indicated that TUBG1 and TUBG2 are not functionally equivalent in vivo, that TUBG1 corresponds to conventional γ-tubulin, and that TUBG2 may have some unidentified function in the brain.
Original language | English |
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Pages (from-to) | 361-373 |
Number of pages | 13 |
Journal | Developmental Biology |
Volume | 282 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2005 Jun 15 |
Externally published | Yes |
Keywords
- Gene knockout
- Isoform
- Microtubule
- Mitotic spindle
- γ-Tubulin
ASJC Scopus subject areas
- Molecular Biology
- Developmental Biology
- Cell Biology