Ruprecht-Karls-Universität Heidelberg

Anne Schlaitz
Research Unit

Im Neuenheimer Feld 282
69120 Heidelberg, Germany
Tel. +49 (0) 6221 - 54 6889
Fax +49 (0) 6221 - 54 5892


Microtubule-based mechanisms determining intracellular organization

Cells require a defined architecture to perform their specific functions. Cellular architecture is discernible in the exterior appearance of different cell types but also in their internal organization. The intracellular architecture of a eukaryotic cell is determined by the complement of organelles with their specific positions and shapes and facilitates the cell’s particular role in the organism. Accordingly, intracellular organization is dynamically altered to adapt to new cellular roles during processes such as development and polarization. In diseased cells, on the other hand, intracellular architecture can be significantly transformed. The remodeling of tumor cells, for instance, precedes metastatic spreading of most cancers. Furthermore, intracellular architecture is adjusted throughout the cell cycle, most obviously during mitosis to allow faithful division of chromosomes and other cellular contents.
To date, only few proteins are known that can bring about the structural changes in organelle shape and positioning necessary for intracellular remodeling.
Intracellular remodeling often involves the microtubule cytoskeleton in addition to membrane-bound organelles. Thus, proteins that associate with both microtubules and organelles may coordinate the reorganization of microtubules and organelles. These linker proteins are therefore promising candidates for new effectors of intracellular remodeling. With a biochemical screening approach we have previously identified new candidate linkers between organelles and microtubules. We found that the uncharacterized linkers REEP3 and REEP4 govern the shape and distribution of the endoplasmic reticulum (ER) during cell division. We speculate that other linker proteins identified also help to restructure organelles during various cellular remodeling events.
Research in the lab aims at (1) further elucidating the mechanisms of REEP3/4 function, (2) characterizing remodeling and functions of membrane-bound organelles during cell division, and (3) uncovering roles of organelle-microtubule linker proteins in cell polarization and differentiation.

Selected publications

Kumar D, Golchoubian B, Belevich I, Jokitalo E, Schlaitz A. REEP3 and REEP4 Determine the Tubular Morphology of the Endoplasmic Reticulum during Mitosis. Mol Biol Cell, 2019.

Schlaitz AL. Microtubules as key coordinators of nuclear envelope and endoplasmic reticulum dynamics during mitosis. Bioessays, 2014.

Schlaitz AL, Thompson J, Wong CC, Yates JR and Heald R. REEP3/4 ensure endoplasmic reticulum clearance from metaphase chromatin and proper nuclear envelope architecture. Developmental Cell, 2013.

Schlaitz AL, Srayko M, Dammermann A, Quintin S, Wielsch N, MacLeod I, de Robillard Q, Zinke A, Yates III JR, Muller-Reichert T, Shevchenko A, Oegema K, Hyman AA. The C. elegans RSA complex localizes Protein Phosphatase 2A to centrosomes and regulates mitotic spindle assembly. Cell, 2007.



Reorganization of microtubules and endoplasmic reticulum (ER) during mitosis.

In interphase, microtubules and ER form extensive networks throughout the cytoplasm that appear unfocused or have one focus at the centrosome. In metaphase, the microtubule cytoskeleton forms the bipolar mitotic spindle. ER is enriched at spindle poles but remains excluded from the central spindle area and chromosomes.


The linker proteins REEP3 and REEP4 govern mitotic ER distribution.

In metaphase cells depleted of REEP3/4 ER invades the spindle area and accumulates on chromosomes.
(Figures modified from Schlaitz, AL, Bioessays, 2014)