Slit (protein)

Last updated
slit
Identifiers
Organism Drosophila melanogaster
Symbolsli
Entrez 36746
RefSeq (mRNA) NM_057381.3
RefSeq (Prot) NP_476729.1
UniProt P24014
Other data
Chromosome 2R: 11.75 - 11.82 Mb
slit homolog 1
Identifiers
Symbol SLIT1
Alt. symbolsSLIL1
NCBI gene 6585
HGNC 11085
OMIM 603742
RefSeq NM_003061
UniProt O75093
Other data
Locus Chr. 10 q23.3-q24
slit homolog 2
Identifiers
Symbol SLIT2
Alt. symbolsSLIL3
NCBI gene 9353
HGNC 11086
OMIM 603746
RefSeq NM_004787
UniProt O94813
Other data
Locus Chr. 4 p15.2
slit homolog 3
Identifiers
Symbol SLIT3
Alt. symbolsSLIL2
NCBI gene 6586
HGNC 11087
OMIM 603745
RefSeq NM_003062
UniProt O75094
Other data
Locus Chr. 5 q35

Slit is a family of secreted extracellular matrix proteins which play an important signalling role in the neural development of most bilaterians (animals with bilateral symmetry). While lower animal species, including insects and nematode worms, possess a single Slit gene, humans, mice and other vertebrates possess three Slit homologs: Slit1, Slit2 and Slit3. Human Slits have been shown to be involved in certain pathological conditions, such as cancer and inflammation. [1]

Contents

The ventral midline of the central nervous system is a key place where axons can either decide to cross and laterally project or stay on the same side of the brain. [2] The main function of Slit proteins is to act as midline repellents, preventing the crossing of longitudinal axons through the midline of the central nervous system of most bilaterian animal species, including mice, chickens, humans, insects, nematode worms and planarians. [3] It also prevents the recrossing of commissural axons. Its canonical receptor is Robo but it may have other receptors. The Slit protein is produced and secreted by cells within the floor plate (in vertebrates) or by midline glia (in insects) and diffuses outward. Slit/Robo signaling is important in pioneer axon guidance. [4]

Discovery

Slit mutations were first discovered in the Nuesslein-Volhard/Wieschaus patterning screen where they were seen to affect the external midline structures in the embryos of Drosophila melanogaster , also known as the common fruit fly. In this experiment, researchers screened for different mutations in D. melanogaster embryos that affected the neural development of axons in the central nervous system. They found that the mutations in commissureless genes (Slit genes) lead to the growth cones that typically cross the midline remaining on their own side. The findings from this screening suggest that Slit genes are responsible for repulsive signaling along the neuronal midline. [5]

Structure

Slit1, Slit2, and Slit3 each have the same basic structure. A major identifying feature of the Slit protein is the four leucine-rich repeat (LRR) domains and the N-terminus. Slits are one of only two protein families that contain multiple LRR domains. These LRRs are followed by six repeats similar to epidermal growth factors (EGF) as well as a β-sandwich domain similar to laminin G. Directly after these sequences, invertebrates have one EGF repeat, whereas vertebrates have three EGF repeats. In each case, the EGF is followed by a C-terminal cystine knot (CT) domain. [6]

It is possible for Slits to be cleaved into fragments of the N-terminus and C-terminus as a result of an assumed proteolytic site between the fifth and sixth EGFs in Drosophila Slit, Caenorhabditis elegans Slit, rat Slit1, rat Slit3 and human Slit2. [7]

LRR domains

Horseshoe-shaped LRR Domain 2bnh topview.png
Horseshoe-shaped LRR Domain

Slit LRR domains are thought to assist in controlling neurite outgrowth. The domains consist of five to seven LRRs each with disulfide-rich cap segments. Each LRR motif contains a LXXLXLXXN sequence (where L = leucine, N = asparagine, X = any amino acid) which is one strand to a parallel β-sheet on the concave face of the LRR domain, while the back side of the domain consists of irregular loops. Each of the four domains of Slit are connected by short "linkers" which attach to the domains via a disulfide bridge, allowing the LRR region of Slit to remain very compact. [6]

Vertebrate homologs

Slit1, Slit2, and Slit3 are all a human homologs of the 'Slit' gene found in Drosophila. Each of these genes secretes a protein containing protein-protein interaction regions with leucine-rich repeats and EFGs. Slit2 is mainly expressed in the spinal cord, where it repels motor axons. Slit1 functions in the brain, and Slit3 in the thyroid. Both Slit1 and Slit2 are found in the murine postnatal septum as well as in the neocortex. Further, Slit2 participates in inhibiting leukocyte chemotaxis. In rats, Slit1 was found in the neurons of adult and fetal forebrains. This shows that Slit proteins in mammals most likely contribute to the process of forming and maintaining the endocrine and nervous systems through interactions between proteins. [8] Slit3 is primarily expressed in the thyroid, in human umbilical vein endothelial cells (HUVECs), as well as in endothelial cells from the lung and diaphragm of the mouse. Slit3 interacts with Robo1 and Robo4. [9]

Function

Guidance molecules

Slit and Robo Interactions Slit and Robo Interactions.png
Slit and Robo Interactions

Guidance molecules act as cues by carrying information to receptive cells; administering this information which tells the cell and its entities how to properly align. [10] Slit proteins behave as such when working in axonal guidance during the development of the nervous system. Similarly, these proteins help to orchestrate the development of various networks of tissues throughout the body. This role, also described as cell migration, is the primary role of Slit when interacting with Robo. It is most commonly found acting in neurons, endothelial cells and cancer cells. [10]

Axon guidance

A diagram illustrating the role of Slit in axon guidance: When bound to the cells of the midline, Slit acts by signaling with Robo to repel growing axons away from the midline. Slit and Axon Guidance.png
A diagram illustrating the role of Slit in axon guidance: When bound to the cells of the midline, Slit acts by signaling with Robo to repel growing axons away from the midline.

Chemorepellents help to direct growing axons toward the correct regions by directing them away from inappropriate regions. Slit genes, as well as their roundabout receptors, act as chemorepellents by helping prevent the wrong types of axons from crossing the midline of the central nervous system during establishment or remodeling of the neural circuits. The binding of Slit to any member of the Roundabout receptor family results in axon repelling through changes in the axon growth cone. The resulting repelling of axons is collectively termed as axonal guidance. Slit1 and Slit2 have both been seen to collapse and repel olfactory axons. Further evidence suggests that Slit also directs interneurons, particularly acting in the cortex. [11] Positive effects are also correlated with slits. Slit2 begins the formation of axon branches through neural growth factor genes of the dorsal root ganglia.

Organogenesis

Several studies have shown that the interaction of Slit with its receptors is crucial in regulating the processes involved with the formation of organs. As previously discussed, these interactions play a key role in cell migration. Not surprisingly then, this gene has been found expressed during the development of tightly regulated tissues, such as the heart, lungs, gonads, and ovaries. For example, in early development of the heart tube in Drosophila, Slit and two of its Robo receptors guide migrating cardioblasts and pericardial cells in the dorsal midline. [7] In addition, research on mice has shown that Slit3 and its interaction with Robo1 may be crucial to the development and maturation of lung tissue. Similarly, the expression of Slit3 is upregulated when aligning airway epithelium with endothelium. [10] Due to its regulating function in tissue development, absence or mutations in the expression of these genes can result in abnormalities of these tissues. Several studies in mice and other vertebrates have shown that this deficit results in death almost immediately after birth.

Angiogenesis

The Slit2 protein has recently been discovered to be associated with the development of new blood vessels from pre-existing vessels, or angiogenesis. Recent research has debated on whether this gene inhibits or stimulates this process. There has been significant proof to conclude that both are true, depending on the context. It has been concluded that the role of Slit in this process depends on which receptor it binds, the cellular context of its target cells, and/or other environmental factors. [12] Slit2 has been implicated in promoting angiogenesis in mice (both in vitro and in vivo), in the human placenta, [12] and in tumorigenesis. [13]

Clinical importance

Because of their part in forebrain development, during which they contribute to axonal guidance and guiding signals in the movement of cortical interneurons, Slit-Robo signal transduction mechanisms could possibly be used in therapy and treatment of neurological disorders and certain types of cancer. [11] Procedures have been found in which Slit genes allow for precise control over vascular guidance cues influencing the organization of blood vessels during development. [14] Slit also plays a large role in angiogenesis. With increased knowledge of this relationship, treatments could be developed for complications with development of embryo vasculature, female reproductive cycling, tumor grown, and metastasis, ischemic cardiovascular diseases, or ocular disorders. [15]

Cancer

Due to its pivotal role in controlling cell migration, abnormalities or absences in the expression of Slit1, Slit2 and Slit3 are associated with a variety of cancers. In particular, Slit-Robo interaction has been implicated in reproductive and hormone dependent cancers, particularly in females. Under normal function, these genes act as tumor suppressors. Therefore, deletion or lack of expression of these genes is associated with tumorigenesis, particularly tumors within the epithelium of the ovaries, endometrium, and cervix. Samples of surface epithelium in cancer ridden ovaries has exhibited that these cells show decreased expression of Slit2 and Slit3. In addition, absence of these genes allows the migration of cancer cells and thus is associated with increased cancer progression and increased metastasis. [7] The role of this gene and its place in cancer treatment and development is becoming increasingly unraveled but increasingly complex.

Related Research Articles

<span class="mw-page-title-main">Retinal ganglion cell</span> Type of cell within the eye

A retinal ganglion cell (RGC) is a type of neuron located near the inner surface of the retina of the eye. It receives visual information from photoreceptors via two intermediate neuron types: bipolar cells and retina amacrine cells. Retina amacrine cells, particularly narrow field cells, are important for creating functional subunits within the ganglion cell layer and making it so that ganglion cells can observe a small dot moving a small distance. Retinal ganglion cells collectively transmit image-forming and non-image forming visual information from the retina in the form of action potential to several regions in the thalamus, hypothalamus, and mesencephalon, or midbrain.

<span class="mw-page-title-main">Notch signaling pathway</span> Series of molecular signals

The Notch signaling pathway is a highly conserved cell signaling system present in most animals. Mammals possess four different notch receptors, referred to as NOTCH1, NOTCH2, NOTCH3, and NOTCH4. The notch receptor is a single-pass transmembrane receptor protein. It is a hetero-oligomer composed of a large extracellular portion, which associates in a calcium-dependent, non-covalent interaction with a smaller piece of the notch protein composed of a short extracellular region, a single transmembrane-pass, and a small intracellular region.

Axon guidance is a subfield of neural development concerning the process by which neurons send out axons to reach their correct targets. Axons often follow very precise paths in the nervous system, and how they manage to find their way so accurately is an area of ongoing research.

<span class="mw-page-title-main">Netrin</span> Class of proteins involved in axon guidance

Netrins are a class of proteins involved in axon guidance. They are named after the Sanskrit word "netr", which means "one who guides". Netrins are genetically conserved across nematode worms, fruit flies, frogs, mice, and humans. Structurally, netrin resembles the extracellular matrix protein laminin.

<span class="mw-page-title-main">Floor plate</span> Embryonic structure

The floor plate is a structure integral to the developing nervous system of vertebrate organisms. Located on the ventral midline of the embryonic neural tube, the floor plate is a specialized glial structure that spans the anteroposterior axis from the midbrain to the tail regions. It has been shown that the floor plate is conserved among vertebrates, such as zebrafish and mice, with homologous structures in invertebrates such as the fruit fly Drosophila and the nematode C. elegans. Functionally, the structure serves as an organizer to ventralize tissues in the embryo as well as to guide neuronal positioning and differentiation along the dorsoventral axis of the neural tube.

<span class="mw-page-title-main">Ephrin receptor</span> Protein family

Eph receptors are a group of receptors that are activated in response to binding with Eph receptor-interacting proteins (Ephrins). Ephs form the largest known subfamily of receptor tyrosine kinases (RTKs). Both Eph receptors and their corresponding ephrin ligands are membrane-bound proteins that require direct cell-cell interactions for Eph receptor activation. Eph/ephrin signaling has been implicated in the regulation of a host of processes critical to embryonic development including axon guidance, formation of tissue boundaries, cell migration, and segmentation. Additionally, Eph/ephrin signaling has been identified to play a critical role in the maintenance of several processes during adulthood including long-term potentiation, angiogenesis, and stem cell differentiation and cancer.

<span class="mw-page-title-main">Netrin receptor DCC</span> Protein-coding gene in the species Homo sapiens

Netrin receptor DCC, also known as DCC, or colorectal cancer suppressor is a protein which in humans is encoded by the DCC gene. DCC has long been implicated in colorectal cancer and its previous name was Deleted in colorectal carcinoma. Netrin receptor DCC is a single transmembrane receptor.

Pioneer axon is the classification given to axons that are the first to grow in a particular region. They originate from pioneer neurons, and have the main function of laying down the initial growing path that subsequent growing axons, dubbed follower axons, from other neurons will eventually follow.

<span class="mw-page-title-main">Ephrin</span>

Ephrins are a family of proteins that serve as the ligands of the Eph receptor. Eph receptors in turn compose the largest known subfamily of receptor protein-tyrosine kinases (RTKs).

<span class="mw-page-title-main">Plexin</span> Protein

A plexin is a protein which acts as a receptor for semaphorin family signaling proteins. It is classically known for its expression on the surface of axon growth cones and involvement in signal transduction to steer axon growth away from the source of semaphorin. Plexin also has implications in development of other body systems by activating GTPase enzymes to induce a number of intracellular biochemical changes leading to a variety of downstream effects.

<span class="mw-page-title-main">Neurexin</span>

Neurexins (NRXN) are a family of presynaptic cell adhesion proteins that have roles in connecting neurons at the synapse. They are located mostly on the presynaptic membrane and contain a single transmembrane domain. The extracellular domain interacts with proteins in the synaptic cleft, most notably neuroligin, while the intracellular cytoplasmic portion interacts with proteins associated with exocytosis. Neurexin and neuroligin "shake hands," resulting in the connection between the two neurons and the production of a synapse. Neurexins mediate signaling across the synapse, and influence the properties of neural networks by synapse specificity. Neurexins were discovered as receptors for α-latrotoxin, a vertebrate-specific toxin in black widow spider venom that binds to presynaptic receptors and induces massive neurotransmitter release. In humans, alterations in genes encoding neurexins are implicated in autism and other cognitive diseases, such as Tourette syndrome and schizophrenia.

Faint little ball (flb) is a Drosophila gene that encodes the Drosophila epidermal growth factor receptor (DER) homolog. The gene is also called torpedo and Ellipse. The gene is located at 3-26 of the Drosophila melanogaster genome. It is named faint little ball because when the gene is mutated the embryo forms a ball of dorsal hypoderm. flb is necessary for several processes to occur during embryonic development, specifically in central nervous system development. It is expressed as quickly as 4 hours after fertilization of the egg. The peak of expression of the flb gene is between 4–8 hours into development. In all processes that are facilitated by flb the same signal transduction pathway is used. Drosophila EGF receptor is involved in the development of embryos as well as larvae/pupae's wings, eyes, legs and ovaries.

<span class="mw-page-title-main">SLIT2</span>

Slit homolog 2 protein is a protein that in humans is encoded by the SLIT2 gene.

<span class="mw-page-title-main">ROBO1</span>

Roundabout homolog 1 is a protein that in humans is encoded by the ROBO1 gene.

<span class="mw-page-title-main">SLIT1</span> Mammalian protein found in Homo sapiens

Slit homolog 1 protein is a protein that in humans is encoded by the SLIT1 gene.

<span class="mw-page-title-main">ROBO2</span>

Roundabout homolog 2 is a protein that in humans is encoded by the ROBO2 gene.

<span class="mw-page-title-main">Roundabout family</span>

The Roundabout (Robo) family of proteins are single-pass transmembrane receptors that are highly conserved across many branches of the animal kingdom, from C. elegans to humans. They were first discovered in Drosophila, through a mutant screen for genes involved in axon guidance. The Drosophila roundabout mutant was named after its phenotype, which resembled the circular traffic junctions. The Robo receptors are most well known for their role in the development of the nervous system, where they have been shown to respond to secreted Slit ligands. One well-studied example is the requirement for Slit-Robo signaling in regulation of axonal midline crossing. Slit-Robo signaling is also critical for many neurodevelopmental processes including formation of the olfactory tract, the optic nerve, and motor axon fasciculation. In addition, Slit-Robo signaling contributes to cell migration and the development of other tissues such as the lung, kidney, liver, muscle and breast. Mutations in Robo genes have been linked to multiple neurodevelopmental disorders in humans.

<span class="mw-page-title-main">Death domain</span>

The death domain (DD) is a protein interaction module composed of a bundle of six alpha-helices. DD is a subclass of protein motif known as the death fold and is related in sequence and structure to the death effector domain (DED) and the caspase recruitment domain (CARD), which work in similar pathways and show similar interaction properties. DD bind each other forming oligomers. Mammals have numerous and diverse DD-containing proteins. Within these proteins, the DD domains can be found in combination with other domains, including: CARDs, DEDs, ankyrin repeats, caspase-like folds, kinase domains, leucine zippers, leucine-rich repeats (LRR), TIR domains, and ZU5 domains.

Slit-Robo is the name of a cell signaling protein complex with many diverse functions including axon guidance and angiogenesis.

<span class="mw-page-title-main">Tropic cues involved in growth cone guidance</span>

The growth cone is a highly dynamic structure of the developing neuron, changing directionality in response to different secreted and contact-dependent guidance cues; it navigates through the developing nervous system in search of its target. The migration of the growth cone is mediated through the interaction of numerous trophic and tropic factors; netrins, slits, ephrins and semaphorins are four well-studied tropic cues (Fig.1). The growth cone is capable of modifying its sensitivity to these guidance molecules as it migrates to its target; this sensitivity regulation is an important theme seen throughout development.

References

  1. Hohenester E (April 2008). "Structural insight into Slit-Robo signalling". Biochem. Soc. Trans. 36 (Pt 2): 251–6. doi:10.1042/BST0360251. PMID   18363568.
  2. Erskine L, Williams SE, Brose K, Kidd T, Rachel RA, Goodman CS, Tessier-Lavigne M, Mason CA (July 2000). "Retinal ganglion cell axon guidance in the mouse optic chiasm: expression and function of robos and slits". J. Neurosci. 20 (13): 4975–82. doi:10.1523/JNEUROSCI.20-13-04975.2000. PMC   6772295 . PMID   10864955.
  3. Brose K, Bland KS, Wang KH, Arnott D, Henzel W, Goodman CS, Tessier-Lavigne M, Kidd T (March 1999). "Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance". Cell. 96 (6): 795–806. doi: 10.1016/S0092-8674(00)80590-5 . PMID   10102268. S2CID   16301178.
  4. Farmer WT, Altick AL, Nural HF, Dugan JP, Kidd T, Charron F, Mastick GS (November 2008). "Pioneer longitudinal axons navigate using floor plate and Slit/Robo signals". Development. 135 (22): 3643–53. doi:10.1242/dev.023325. PMC   2768610 . PMID   18842816.
  5. Seeger M, Tear G, Ferres-Marco D, Goodman CS (March 1993). "Mutations affecting growth cone guidance in Drosophila: genes necessary for guidance toward or away from the midline". Neuron. 10 (3): 409–26. doi:10.1016/0896-6273(93)90330-T. PMID   8461134. S2CID   21594847.
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  7. 1 2 3 Dickinson RE, Duncan WC (April 2010). "The SLIT-ROBO pathway: a regulator of cell function with implications for the reproductive system". Reproduction. 139 (4): 697–704. doi:10.1530/REP-10-0017. PMC   2971463 . PMID   20100881.
  8. Online Mendelian Inheritance in Man (OMIM): 603746
  9. Online Mendelian Inheritance in Man (OMIM): 603745
  10. 1 2 3 Nasarre P, Potiron V, Drabkin H, Roche J (2010). "Guidance molecules in lung cancer". Cell Adh Migr. 4 (1): 130–45. doi:10.4161/cam.4.1.10882. PMC   2852570 . PMID   20139699.
  11. 1 2 Andrews WD, Barber M, Parnavelas JG (August 2007). "Slit-Robo interactions during cortical development". J. Anat. 211 (2): 188–98. doi:10.1111/j.1469-7580.2007.00750.x. PMC   2375773 . PMID   17553100.
  12. 1 2 Liao WX, Wing DA, Geng JG, Chen DB (September 2010). "Perspectives of SLIT/ROBO signaling in placental angiogenesis" (PDF). Histol. Histopathol. 25 (9): 1181–90. PMC   8900672 . PMID   20607660.
  13. Klagsbrun M, Eichmann A (2005). "A role for axon guidance receptors and ligands in blood vessel development and tumor angiogenesis". Cytokine Growth Factor Rev. 16 (4–5): 535–48. doi:10.1016/j.cytogfr.2005.05.002. PMID   15979925.
  14. Small EM, Sutherland LB, Rajagopalan KN, Wang S, Olson EN (November 2010). "MicroRNA-218 regulates vascular patterning by modulation of Slit-Robo signaling". Circ. Res. 107 (11): 1336–44. doi:10.1161/CIRCRESAHA.110.227926. PMC   2997642 . PMID   20947829.
  15. Chen H, Zhang M, Tang S, London NR, Li DY, Zhang K (2010). "Slit-Robo signaling in ocular angiogenesis". Adv. Exp. Med. Biol. Advances in Experimental Medicine and Biology. 664: 457–63. doi:10.1007/978-1-4419-1399-9_52. ISBN   978-1-4419-1398-2. PMID   20238047.