Ordered assembly of the duplicating Golgi in Trypanosoma brucei

Proc Natl Acad Sci U S A. 2006 May 16;103(20):7676-81. doi: 10.1073/pnas.0602595103. Epub 2006 May 3.

Abstract

The new Golgi in the protozoan parasite Trypanosoma brucei grows near to the old and adjacent to the growing new endoplasmic reticulum exit site. Growth is now shown to be at least a two-stage process, in which a representative matrix marker (GRASP) and enzyme (GntB) are delivered to the site of assembly, followed approximately 10 min later by a COPI component (epsilon-COP) and a trans-Golgi network (TGN) marker (GRIP70). A secretory cargo marker (signal sequence-YFP) appeared early near the new endoplasmic reticulum exit site but did not enter the Golgi until the second stage. Together these data suggest that structural and enzymatic components of the new Golgi stack are laid down first, followed by those needed to move and sort the cargo passing through it.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biological Transport / physiology
  • Biomarkers / metabolism*
  • Carrier Proteins / metabolism
  • Coat Protein Complex I / metabolism
  • Golgi Apparatus / chemistry
  • Golgi Apparatus / physiology*
  • Golgi Apparatus / ultrastructure
  • Luminescent Proteins / metabolism
  • Membrane Proteins / metabolism
  • Protozoan Proteins / metabolism*
  • Trypanosoma brucei brucei* / cytology
  • Trypanosoma brucei brucei* / metabolism

Substances

  • Biomarkers
  • Carrier Proteins
  • Coat Protein Complex I
  • Luminescent Proteins
  • Membrane Proteins
  • Protozoan Proteins