Faber Klaas Nico, Haan Gert Jan, Baerends Richard J S, Kram Anita M, Veenhuis Marten
Eukaryotic Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Postbus 14, 9750 AA Haren, The Netherlands.
J Biol Chem. 2002 Mar 29;277(13):11026-33. doi: 10.1074/jbc.M112347200. Epub 2002 Jan 14.
We show that the synthesis of the N-terminal 50 amino acids of Pex3p (Pex3p(1-50)) in Hansenula polymorpha pex3 cells is associated with the formation of vesicular membrane structures. Biochemical and ultrastructural findings suggest that the nuclear membrane is the donor membrane compartment of these vesicles. These structures also contain Pex14p and can develop into functional peroxisomes after subsequent reintroduction of the full-length Pex3p protein. We discuss the significance of this finding in relation to peroxisome reintroduction, e.g. in case peroxisomes are lost due to failure in inheritance.
我们发现,多形汉逊酵母pex3细胞中Pex3p(Pex3p(1-50))N端50个氨基酸的合成与囊泡膜结构的形成有关。生化和超微结构研究结果表明,核膜是这些囊泡的供体膜区室。这些结构还含有Pex14p,在随后重新引入全长Pex3p蛋白后可发育成功能性过氧化物酶体。我们讨论了这一发现与过氧化物酶体重建的相关性,例如在过氧化物酶体因遗传失败而丢失的情况下。