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The Bbp1p–Mps2p complex connects the SPB to the nuclear envelope and is essential for SPB duplication
Author(s) -
Schramm Carolin,
Elliott Sarah,
Shevchenko Anna,
Shevchenko Andrej,
Schiebel Elmar
Publication year - 2000
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/19.3.421
Subject(s) - biology , gene duplication , envelope (radar) , genetics , evolutionary biology , computational biology , gene , telecommunications , radar , computer science
In budding yeast, microtubules are organized by the spindle pole body (SPB), which is embedded in the nuclear envelope via its central plaque structure. Here, we describe the identification of BBP1 in a suppressor screen with a conditional lethal allele of SPC29 . Bbp1p was detected at the central plaque periphery of the SPB and bbp1‐1 cells were found to be defective in SPB duplication. bbp1‐1 cells extend their satellite into a duplication plaque like wild‐type cells; however, this duplication plaque then fails to insert properly into the nuclear envelope and does not assemble a functional inner plaque. This function in SPB duplication is probably fulfilled by a stable complex of Bbp1p and Mps2p, a nuclear envelope protein that is also essential for duplication plaque insertion. In addition, we found that Bbp1p interacts with Spc29p and the half‐bridge component Kar1p. These interactions are likely to play a role in connecting the SPB with the nuclear envelope and the central plaque with the half‐bridge.