User:Alisa Cario

Introduction and Background

The cytoskeleton brings structure to the cell, is integral in cell division, and aids in migration. One of the constitutive parts of the cytoskeleton are microtubules. Microtubules are polymerized from tubulin subunits that incorporate into a hollow cylindrical structure linked together by lateral and vertical hydrogen bonds between heterodimers. Each tubulin subunit is made from a heterodimer of alpha and beta tubulin. Both alpha and beta tubulin are known to bind to GTP. However, only the beta subunit hydrolyzes GTP once incorporated into microtubules. The beta tubulin hydrolysis of GTP to GDP is known to destabilize microtubules. Microtubules have polarity where one end of microtubule, called the plus end, has more a greater affinity to add tubulin subunits than the other end, called the minus end. Microtubules are inherently dynamic, going through periods of depolymerization, known as catastrophe, and then return to polymerization, known as rescue. Microtubules can also go through a process called tread milling, where the length of the microtubule does not change but the rate of polymerization at the plus end equals the rate of depolymerization at the minus end. There are a number of microtubule associated proteins (MAPs) that are known to regulate the dynamics of microtubules. Some examples of this are KIF family kinesin motors, tau, MAP2 and stathmin.

Figure XXX. Stathmin in purple can bind to tubulin dimers to prevent polymerization or to microtubules to increase catastrophe

Function

Stathmin, also known as oncoprotein 18 or metablastin, is a 19kDa microtubule associated protein known to destabilize microtubules. Stathmin's many names come from the fact that different labs discovered the protein during the same time. Stathmin is a cell cycle and developmentally regulated protein and is known to play a role in proliferation, differentiation and function of cells. ( ) Stathmin can bind to tubulin dimers to inhibit polymerization or it can bind to the microtubule to enhance the rate of catastrophe. This is shown in Figure XXX. Stathmin, shown in purple, can bind to tubulin heterodimers or microtubules , shown in green.

Figure XXX. Stathmin in purple can bind to tubulin dimers to prevent polymerization or to microtubules to increase catastrophe

Mitosis Stathmin's role in the cell cycle progression is well characterized. During interphase, microtubules are relatively stable. However during the onset of mitosis, stathmin is upregulated to increase the rate of catastrophe of microtubules, causing them to become more dynamic (1). Stathmin has also been shown to bind and sequester two tubulin heterodimers, reducing the amount of available tubulin to polymerize microtubules (2). However, as mitosis progresses, microtubules must repolymerize to form the mitotic spindle. Stathmin is regulated during this process by phosphorylation ( ). There are four known phosphorylation sites of stathmin, serine 16, serine 25, serine 38, and serine 63. Stathmin is the known target of cyclin-dependent kinases ( ). Stathmin overexpression prevents mitotic spindle formation where inhibition interferes with later stages in mitosis.

Figure XXX.

Migration

The cytoskeleton is a vital part of cell migration. The leading edge is driven by actin polymerization. However, microtubules are needed to retract from the trailing edge to move the cell forward. Stathmin is thought to have a similar role in migration, allowing to microtubules to depolymerize to aid in movement. Stathmin is part of the integrin alpha5 beta1/FAK/ ERK pathway.

Differentiation

Stathmin expression is regulated during stages of development. It is regulated in early and late embryogenesis. It is also regulated in differentiating muscle cells, T lymphocytes, and oligodendryocytes.

Structural highlights

How does the structure relate to it's function?

Stathmin is not A structurally complicated the protein, consisting of a single alpha helix, that binds across two tubulin heterodimers, and a mostly disordered N-terminal region that also has some beta strand properties. These different regions of the protein are known to have different functions.

The N-terminal region is known to increase tubulin catastrophe. This region helps destabilize the ends of the microtubule filaments by curving the tubulin dimers at the end, and disrupting lateral hydrogen bonds. The N-terminal region is known as the regulatory domain of the protein, because it is subject to most of the post-translational modifications. This region binds and caps alpha tubulin to accomplish this task. ( ) 4.

The C-terminal region, also known as the interaction domain, is known to sequester tubulin heterodimers. This region is comprised of a coiled-coil single alpha helix. This region of stathmin is known to bind to helix 10 of alpha tubulin. Helix 10 of alpha tubulin is known to be important for incorporation into microtubules.

The structure of stathmin, in 4eb6, is stabilized by outside ligands. Vinblastine, is a _____. Also, there are two known mutations in the protein.

TALK ABOUT VBL TALK ABOUT MUTATIONS

Figure XXX.

Disease relevance

Multiple Schlerosis Brain tissue samples from people suffering from multiple schlerosis found that stathmin is unregulated in oligodendrocytes. The up-regulation of stathmin showed instability in oligodendrocyte microtubules leading to a more globular morphology of the cells. Oligodendrocyte ability to myelinate axons in the central nervous system was greatly reduced (REFERENCE).

Cancer Due to stathmin's role in mitosis and cell migration, it is not surprising that is has been implicated in many cancers and is an active target of cancer therapeutics. Overexpression of stathmin has been shown to increase metastasis, worse prognosis, and increased chemoresistance. Stathmin levels are known to be increasesd in a number of cancers including but not limited to breast cancer, ovarian cancer, bladder cancer, etc. Stathmin was seen to be upregulated in breast cancer tissue comparative with normal breast tissue ( ). Other study was done to show stathmin-1 upregulation in esophageal squamous cell carcinomas ( ). Studies using a non-phosphorylatable stathmin mutant shows that cells arrest during mitosis (Marklund, Larson)

Evolutionary conservation

Stathmin belongs to a gene family. This family includes SCG10 and SCILP, which are neuronal proteins. Other members of this family of proteins include XB3, which was discovered in Xenopus (34 from https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1432-1033.1997.t01-2-00794.x)

Isoforms

There are four isoforms of stathmin which are alternatively spliced from a single gene in . Stathmin 1-3 are expressed early in development DEVELOPMENTAL REGULATION LOCATION OF ISOFORMS HOW THEY DIFFER

Links to available structures

References

1. Belmont LD, Mitchison TJ. 1996. Identification of a proteinthat interacts with tubulin dimers and increases thecatastrophe rate of microtubules. Cell 84:623–631

2. Jourdain L, Curmi P, Sobel A, Pantaloni D, Carlier M-F.1997. Stathmin: A tubulin-sequestering protein whichforms a ternary T2S complex with two tubulin molecules.Biochemistry 36:10817–10821.

3. Howell B, Larsson N, Gullberg M, Cassimeris L. 1999.Dissociation of the tubulin-sequestering and microtubulecatastrophe-promoting activities of oncoprotein 18/stath-min. Mol Biol Cell 10:105–118.

Tournebize, R., Andersen, S. S., Verde, F., Dore ́e, M., Karsenti, E., andHyman, A. A. (1997) EMBO J. 16, 5537–5549

L arssonN,MelanderH,MarklundU,Osterman0andGullbergM (1995)G2/M transition requires multisite phosphorylation of oncoprotein 18 by two distinct protein kinase systems. J Biol Chem 270: 14175-14183

LarssonN,MarklundU,GradinHM,BrattsandGandGullbergM (1997)Controlof microtubule dynamics by oncoprotein 18: dissection of the regulatory role of multisite phosphorylation during mitosis. Mol Cell Biol 17: 553(-5539

Lawler S, Gavet 0, Rich T and Sobel A (1998) Stathmin overexpression in 293 cells affectssignaltransductionandthecelcycle.FEBS Lett421:55-60

StrahlerJR,LambBJ,UngarDR,FoxDA andHanashSM (1992)Cellcycle progressionisassociatedwithdistinctpatternsofphosphorylationofOp18. BiochemBiophvsResCommun 185:197-203

http://www.jbc.org/content/268/22/16420.full.pdf