Radial spoke

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The radial spoke is a multi-unit protein structure found in the axonemes of eukaryotic cilia and flagella. [1] Although experiments have determined the importance of the radial spoke in the proper function of these organelles, its structure and mode of action remain poorly understood.

Contents

Cellular location and structure

The radial spoke shown in an axoneme cross-section Eukaryotic flagellum.svg
The radial spoke shown in an axoneme cross-section

Radial spokes are T-shaped structures present inside the axoneme. Each spoke consists of a "head" and a "stalk," while each of these sub-structures is itself made up of many protein subunits. [2] In all, the radial spoke is known to contain at least 17 different proteins, [3] with 5 located in the head and at least 12 making up the stalk. The spoke stalk binds to the A-tubule of each microtubule outer doublet, and the spoke head faces in towards the center of the axoneme (see illustration at right).

Function

The radial spoke is known to play a role in the mechanical movement of the flagellum/cilium. For example, mutant organisms lacking properly functioning radial spokes have flagella and cilia that are immotile. Radial spokes also influence the cilium "waveform"; that is, the exact bending pattern the cilium repeats.

How the radial spoke carries out this function is poorly understood. Radial spokes are believed to interact with both the central pair microtubules and the dynein arms, perhaps in a way that maintains the rhythmic activation of the dynein motors. For example, one of the radial spoke subunits, RSP3, is an anchor protein predicted to hold another protein called protein kinase A (PKA). PKA would theoretically then be able to activate/inactivate the adjacent dynein arms via its kinase activity.

However, the identities and functions of the many radial spoke subunits are just beginning to be elucidated.

Related Research Articles

Microtubule Polymer of tubulin that forms part of the cytoskeleton

Microtubules are polymers of tubulin that form part of the cytoskeleton and provide structure and shape to eukaryotic cells. Microtubules can grow as long as 50 micrometres and are highly dynamic. The outer diameter of a microtubule is between 23 and 27 nm while the inner diameter is between 11 and 15 nm. They are formed by the polymerization of a dimer of two globular proteins, alpha and beta tubulin into protofilaments that can then associate laterally to form a hollow tube, the microtubule. The most common form of a microtubule consists of 13 protofilaments in the tubular arrangement.

Flagellum

A flagellum is a lash-like appendage that protrudes from the cell body of certain bacteria and eukaryotic cells termed as flagellates. A flagellate can have one or several flagella. The primary function of a flagellum is that of locomotion, but it also often functions as a sensory organelle, being sensitive to chemicals and temperatures outside the cell. The similar structure in the archaea functions in the same way but is structurally different and has been termed the archaellum.

Cilium

The cilium is an organelle found on eukaryotic cells in the shape of a slender protuberance that projects from the much larger cell body.

Evolution of flagella Origin of three known varieties of flagella

The evolution of flagella is of great interest to biologists because the three known varieties of flagella each represent a sophisticated cellular structure that requires the interaction of many different systems.

Cytoskeleton Network of filamentous proteins that forms the internal framework of cells

The cytoskeleton is a complex, dynamic network of interlinking protein filaments present in the cytoplasm of all cells, including bacteria and archaea. It extends from the cell nucleus to the cell membrane and is composed of similar proteins in the various organisms. In eukaryotes, it is composed of three main components, microfilaments, intermediate filaments and microtubules, and these are all capable of rapid growth or disassembly dependent on the cell's requirements.

The microtubule-organizing center (MTOC) is a structure found in eukaryotic cells from which microtubules emerge. MTOCs have two main functions: the organization of eukaryotic flagella and cilia and the organization of the mitotic and meiotic spindle apparatus, which separate the chromosomes during cell division. The MTOC is a major site of microtubule nucleation and can be visualized in cells by immunohistochemical detection of γ-tubulin. The morphological characteristics of MTOCs vary between the different phyla and kingdoms. In animals, the two most important types of MTOCs are 1) the basal bodies associated with cilia and flagella and 2) the centrosome associated with spindle formation.

Dynein

Dynein is a family of cytoskeletal motor proteins that move along microtubules in cells. They convert the chemical energy stored in ATP to mechanical work. Dynein transports various cellular cargos, provides forces and displacements important in mitosis, and drives the beat of eukaryotic cilia and flagella. All of these functions rely on dynein's ability to move towards the minus-end of the microtubules, known as retrograde transport, thus, they are called "minus-end directed motors". In contrast, most kinesin motor proteins move toward the microtubules' plus end.

Basal body Protein structure found at the base of cilium or flagellum).

A basal body is a protein structure found at the base of a eukaryotic undulipodium. It is formed from a centriole and several additional protein structures, and is, essentially, a modified centriole. The basal body serves as a nucleation site for the growth of the axoneme microtubules. Centrioles, from which basal bodies are derived, act as anchoring sites for proteins that in turn anchor microtubules, and are known as the microtubule organizing center (MTOC). These microtubules provide structure and facilitate movement of vesicles and organelles within many eukaryotic cells.

Axoneme

An axoneme is the microtubule-based cytoskeletal structure that forms the core of a cilium or flagellum. Cilia and flagella are found on many cells, organisms, and microorganisms, to provide motility. The axoneme serves as the "skeleton" of these organelles, both giving support to the structure and, in some cases, the ability to bend. Though distinctions of function and length may be made between cilia and flagella, the internal structure of the axoneme is common to both.

Motor protein

Motor proteins are a class of molecular motors that can move along the cytoplasm of animal cells. They convert chemical energy into mechanical work by the hydrolysis of ATP. Flagellar rotation, however, is powered by a proton pump.

Intraflagellar transport

Intraflagellar transport or IFT is a bidirectional motility along axonemal microtubules that is essential for the formation (ciliogenesis) and maintenance of most eukaryotic cilia and flagella. It is thought to be required to build all cilia that assemble within a membrane projection from the cell surface. Plasmodium falciparum cilia and the sperm flagella of Drosophila are examples of cilia that assemble in the cytoplasm and do not require IFT. The process of IFT involves movement of large protein complexes called IFT particles or trains from the cell body to the ciliary tip and followed by their return to the cell body. The outward or anterograde movement is powered by kinesin-2 while the inward or retrograde movement is powered by cytoplasmic dynein 2/1b. The IFT particles are composed of about 20 proteins organized in two subcomplexes called complex A and B.

Undulipodium Organelle in locomotion

An undulipodium or a 9+2 organelle is a motile filamentous extracellular projection of eukaryotic cells. It is basically synonymous to flagella and cilia which are differing terms for similar molecular structures used on different types of cells.

Sperm motility describes the ability of sperm to move properly through the female reproductive tract or through water to reach the egg. Sperm motility can also be thought of as the quality, which is a factor in successful conception; sperm that do not "swim" properly will not reach the egg in order to fertilize it. Sperm motility in mammals also facilitates the passage of the sperm through the cumulus oophorus and the zona pellucida, which surround the mammalian oocyte.

Dynactin A 20S multiprotein assembly of total mass about 1.2 MDa that activates dynein-based activity in vivo. A large structural component of the complex is an actin-like 40 nm filament composed of actin-related protein, to which other components attach.

Dynactin is a 23 subunit protein complex that acts as a co-factor for the microtubule motor cytoplasmic dynein-1. It is built around a short filament of actin related protein-1 (Arp1).

KIF3A protein-coding gene in the species Homo sapiens

Kinesin-like protein KIF3A is a protein that in humans is encoded by the KIF3A gene.

DNAI1 protein-coding gene in the species Homo sapiens

Dynein intermediate chain 1, axonemal is a protein that in humans is encoded by the DNAI1 gene.

RSPH4A protein-coding gene in the species Homo sapiens

Radial spoke head protein 4 homolog A, also known as radial spoke head-like protein 3, is a protein that in humans is encoded by the RSPH4A gene.

RSPH6A protein-coding gene in the species Homo sapiens

Radial spoke head protein 6 homolog A (RSPH6A) also known as radial spoke head-like protein 1 (RSHL1) is a protein that in humans is encoded by the RSPH6A gene.

Ciliogenesis is defined as the building of the cell's antenna or extracellular fluid mediation mechanism. It includes the assembly and disassembly of the cilia during the cell cycle. Cilia are important organelles of cells and are involved in numerous activities such as cell signaling, processing developmental signals, and directing the flow of fluids such as mucus over and around cells. Due to the importance of these cell processes, defects in ciliogenesis can lead to numerous human diseases related to non-functioning cilia. Ciliogenesis may also play a role in the development of left/right handedness in humans.

Ian R. Gibbons English biophysicist and cell biologist

Ian Read Gibbons, was a biophysicist and cell biologist. He discovered and named dynein, and demonstrated energy source as ATP is sufficient for dynein to walk on microtubules. In 2017, he and Ronald Vale received the Shaw Prize for their research on microtubule motor proteins.

References

  1. Karp G (19 October 2009). Cell and Molecular Biology: Concepts and Experiments. John Wiley and Sons. pp. 342–. ISBN   978-0-470-48337-4 . Retrieved 25 November 2010.
  2. Yang P, Diener DR, Yang C, Kohno T, Pazour GJ, Dienes JM, Agrin NS, King SM, Sale WS, Kamiya R, Rosenbaum JL, Witman GB (March 2006). "Radial spoke proteins of Chlamydomonas flagella". Journal of Cell Science. 119 (Pt 6): 1165–74. doi:10.1242/jcs.02811. PMC   1973137 . PMID   16507594.
  3. Yang P, Diener DR, Rosenbaum JL, Sale WS (June 2001). "Localization of calmodulin and dynein light chain LC8 in flagellar radial spokes". The Journal of Cell Biology. 153 (6): 1315–26. doi:10.1083/jcb.153.6.1315. PMC   2192029 . PMID   11402073.