Cordon-bleu protein

Protein found in humans

COBL

| Available structures

PDB| Ortholog search: PDBe RCSB
| List of PDB id codes

4PL8

Identifiers
Aliases| COBL, cordon-bleu WH2 repeat protein
External IDs| OMIM: 610317; MGI: 105056; HomoloGene: 9058; GeneCards: COBL; OMA:COBL - orthologs
| Gene location (Human)

Chr.| Chromosome 7 (human)[1]

Band| 7p12.1| Start| 51,016,212 bp[1]
End| 51,316,818 bp[1]
| Gene location (Mouse)

Chr.| Chromosome 11 (mouse)[2]

Band| 11 A1|11 7.3 cM| Start| 12,186,608 bp[2]
End| 12,414,960 bp[2]
| RNA expression pattern

Bgee| | Human| Mouse (ortholog)

|

| Top expressed in

* inferior ganglion of vagus nerve

* parotid gland

* external globus pallidus

* Brodmann area 46

* gastrocnemius muscle

* middle frontal gyrus

* postcentral gyrus

* orbitofrontal cortex

* muscle of thigh

* pars reticulata

| Top expressed in

* muscle of thigh

* esophagus

* temporal muscle

* knee joint

* vastus lateralis muscle

* sternocleidomastoid muscle

* triceps brachii muscle

* ankle

* medial head of gastrocnemius muscle

* skeletal muscle tissue

More reference expression data
BioGPS| | n/a

| Gene ontology

Molecular function|

* actin monomer binding
* actin binding

Cellular component|

* cytoplasm
* dendritic growth cone
* cell projection
* membrane
* ruffle
* plasma membrane
* axonal growth cone
* axon
* soma
* dendrite
* cell cortex
* actin filament
* perinuclear region of cytoplasm
* cytoskeleton

Biological process|

* positive regulation of ruffle assembly
* somite specification
* actin filament network formation
* notochord development
* embryonic axis specification
* positive regulation of dendrite development
* floor plate development
* actin filament polymerization
* neural tube closure
* collateral sprouting in absence of injury
* liver development
* digestive tract development

Sources:Amigo / QuickGO
| Orthologs

Species| Human| Mouse
Entrez| |

23242

12808

Ensembl| |

ENSG00000106078

ENSMUSG00000020173

UniProt| |

O75128

Q5NBX1

RefSeq (mRNA)| | NM_001287436
NM_001287438
NM_015198
NM_001346441
NM_001346442

NM_001346443
NM_001346444

| NM_001282993
NM_001282994
NM_172496
NM_001401095
NM_001401096

NM_001401097
NM_001401098
NM_001401099
NM_001401100

RefSeq (protein)| | NP_001274365
NP_001274367
NP_001333370
NP_001333371
NP_001333372

NP_001333373
NP_056013

| NP_001269922
NP_001269923
NP_766084
NP_001388024
NP_001388025

NP_001388026
NP_001388027
NP_001388028
NP_001388029

Location (UCSC)| Chr 7: 51.02 – 51.32 Mb| Chr 11: 12.19 – 12.41 Mb
PubMed search| [3]| [4]
Wikidata
| View/Edit Human| View/Edit Mouse

|

Protein cordon-bleu is a protein that in humans is encoded by the COBL gene.

The Cordon-bleu protein was first described in 2007.[5] Cobl was demonstrated to be a brain-enriched, Wiskott-Aldrich Homology 2 WH2 domain–based actin nucleator playing a pivotal role in morphogenetic processes in the vertebrate central nervous system (CNS) that give rise to the complex dendritic arbor of neuronal cells.[5][6][7][8][9]

The Cobl gene was originally identified in lacZ-gene-trap experiments in mice.[10] Cobl mRNA was detected as early as at day 7.5 post-coitum (E7.5) in the gastrula organizer and extended towards the axial midline at E8. The organizer is a small group of embryonal cells that organizes the entire body plan because it gives rise to the axial midline – an important source of patterning and morphogenesis cues.

The human COBL gene encodes a 1261-amino acid protein with a mass of about 136 kDa. The mouse protein is 1337 amino acids long. The cobl gene in mice and human gives rise to a variety of putative splice variants, which, however, have not yet been analyzed at the protein level. Cobl genes seem to be restricted to vertebrates.[11][12][13]

Cobl was discovered as an actin nucleator in F-actin formation assays with brain cytosol depleted for the Arp2/3 complex (the only other actin nucleator known at this time) and with beads coated with the SH3 domain of the actin binding protein 1 (Abp1) mAbp1|SH3P7|HIP-55|drebin-like[14] and with the SH3 domain of syndapin I, respectively, and subsequent yeast-two hybrid screen for putatively responsible components using a brain cDNA library. Cobl was then cloned fully and its neuronal functions were characterized in primary neuronal cultures[5][7][8][9] in functional slices of the cerebellum,[7] at the animal level in zebra fish,[15] and in mice.[16]

The WH2 domain-based actin nucleator Cobl turned out to be critical for the induction of dendritic branches in both hippocampal neurons and Purkinje cells of the cerebellum, as revealed by RNAi experiments.[5][7] Cobl hereby specifically accumulates at nascent dendritic branch sites prior to a burst of local F-actin formation at these sites.[8]

Cobl gives rise to actin filaments by bringing together three actin monomers by the use of its three C-terminal WH2 domains, as shown by in vitro reconstitutions with the purified C-terminus of Cobl. In addition to the three C-terminal WH2 domains, the presence of the linker region L2 between the second and third WH2 domain was also of importance for Cobl-mediated actin nucleation. Cobl assembles non-bundled, unbranched actin filaments.[5]

In contrast to other actin nucleators, which are directly or indirectly via their activators controlled by Rho type GTPases, Cobl hereby is controlled by calcium/calmodulin signalling and by arginine methylation brought about by the arginine methyltransferase 2 PRMT2.[9] Consistently, both CaM inhibitors and inhibitors of arginine methylation fully suppressed Cobl-induced dendritic branch induction. Furthermore, Cobl mutants lacking the PRMT2 binding site or lacking CaM-binding regions failed to power dendritic branching.[8][9] The molecular mechanisms, by which Ca2+ signals control the actin nucleator Cobl, are quite complex and may reflect a high level of fine-tuning Cobl's physiological functions to Ca2+ transients in neuronal cells. Cobl is regulated by Ca2+ signals in at least three distinct ways (Izadi and Hou et al., 2018). These modes involve all three WH2 domains of Cobl, which closely need to work together to nucleate actin effectively.[5] Interestingly, Ca2+/CaM controls not only the actin cytoskeletal aspects of Cobl functions but also its targeting to the plasma membrane - a prerequisite for F-actin-driven force generation shaping the morphology of cells. Mutational analyses showed that both individual CaM-dependent regulatory mechanisms are crucial for Cobl-mediated dendritogenesis.[8] The required recruitment of Cobl to the dendritic plasma membrane is brought about by Cobl's own ability to associate with membrane lipids and by the membrane-binding protein syndapin I, which is critical for Cobl's membrane targeting and function.[6]

## Structure

[edit]

Motifs and domains in Cordon-bleu protein.

An important functional part of this actin-nucleating protein is the C-terminus, which contains 3 Wiskott-Aldrich syndrome protein (WASp) homology 2 (WH2) domains.[5] WH2 domains are able to associate with actin monomers to funnel them into actin filament formation processes. Cobl in humans contains three WH2 domains located at the C-terminus (the first WH2 domain, WH2.1, lies between 1109 and 1129, WH2.2 between 1149 and 1169 and WH2.3 between 1237 and 1257), that are responsible for forming an "actin nucleus" composed of 3 actin monomers from which an actin filament can be further elongated. The cobl-actin-nucleus is thought to remain at the pointed end of the emerging filament leaving the barbed end free for rapid polymerization. Other critical functional parts are the N-terminal Cobl Homology domain, which can also be found in the ancestor of Cobl, Cobl-like \- a protein that is also expressed highly in the nervous system and able to give rise to actin filaments by a mechanism different to Cobl, yet, using in part similar associated components and molecular mechanisms.[17] Cobl Homology domains contain three motifs following the consensus KrRAPpPP (first described as "KRAP" motif of unknown function by Caroll et al., 2003), which represent syndapin I binding sites[6] The polypeptide also contains several further proline-rich sequences, which e.g. bind the SH3 domain of Abp1 and PRMT2.[6][7] Also binding sites for profilin-actin heterodimers have been suggested, selected Ser residues are phosphorylated and two Arginines in the second WH2 domain, which is considered the pace maker of the actin nucleation process were detected to be methylated.[9] In humans there are 5 isoforms of Cobl generated though alternative splicing.

### WH2 domain

[edit]

The WH2 domain is an ~18-21 amino acids actin-binding motif. This domain was first recognized as an essential element for the regulation of the cytoskeleton by the mammalian Wiskott-Aldrich syndrome protein (WASp) and is present in at least 6 classes of proteins WIP/Verprolin, Cibulot, Svv2/CAP, β-Thymosines, WAVE/Scar.[18] WH2 proteins occur in eukaryotes from yeast to mammals, in insect viruses, and in some bacteria. The WH2 domain is found as a modular part of larger proteins and can occur as a tandem repeat. The WH2 domain binds actin monomers and can facilitate the assembly of actin monomers into newly forming actin filaments.[19]

## Function

[edit]

Working model of Cobl-induced actin nucleation.[5][20]

Cobl is responsible for the actin polymerization of filaments with fast-growing barbed ends. Cobl stabilizes a longitudinal actin-GTP dimer by two consecutive WH2 domains and it can interact laterally with another actin monomer to form an actin trimer. Rearrangements of the actin–actin contacts have to occur within this trimer to make a helical nucleus; the third WH2 domain of Cobl has been proposed to interact with the third actin subunit of this trimer. This Cobl-actin tetramer is forming a nucleus to facilitate further G-actin addition. Cobl-mediated actin nucleation is very efficient. In fact already low nanomolar concentrations of Cobl can generate unbranched filaments with similar characteristics as WASp–Arp2/3-complex-mediated actin nucleation.[5] Like Spire-1,[13] The expression of Cobl is mainly restricted to the brain; much weaker expression was detected in other tissues.[5] In neurons, Cobl can be found to be enriched at axonal and dendritic growth cones[5] and at dendritic branch induction sites.[8] Cobl The role of Cobl in neural morphogenesis has been investigated ex vivo in hippocampal neurons in rat-brain[5] and in cerebellar slice cultures using a gene gun approach.[7] Overexpression leads to a strong increase in dendrite formation and branching, whereas RNAi-mediated Cobl depletion results in a reduction of dendrites and of dendritic branching.[5][7] Critical roles of Cobl have also been suggested for microvilli formation of colon cells (Grega-Larson et al.,) and in the organization of sensory systems.[15][16] For further details see section "Cobl deficiencies in different animal systems" below.

## Diseases

[edit]

Recent reports don't give a significant insight on a pivotal clinical role of Cobl. Due to its role in vertebrate neural morphogenesis we can speculate that some neurodegenative disorders may be a consequence of a mutated or less functional Cobl. Cobl seems to play a role in the skeletal asymmetry of the Silver-Russel syndrome; the disease is caused by the duplication of the p11.2-p13 segment of the chromosome 7.[21] Screening studies on patients having neurological disorders didn't report until now (June 2009) a specific involvement of Cobl.

## Cobl deficiencies in different animal systems

[edit]

The cobl gene was originally identified in lacZ-gene-trap experiments.[10] Cobl mRNA was detected as early as at day 7.5 post-coitum (E7.5) in the gastrula organizer and extended towards the axial midline at E8. The organizer is a small group of embryonal cells that organizes the entire body plan because it gives rise to the axial midline – an important source of patterning and morphogenesis cues. The striking accumulation and restriction of Cobl mRNA to the organizer and axial midline structures led to the idea that Cobl is involved in vertebrate axis formation.[10] Unfortunately, the CoblC101 allele obtained by the genetrap experiments[10] is only a weakly hypomorphic allele (Caroll et al., 2003) and mice homozygous for the CoblC101 gene-trap allele did not show any obvious phenotype.[10] A genetic interaction with Vangl2 suggested that Cobl has some role in midbrain neural tube closure (Caroll et al., 2003). Cobl knockout mice were viable and showed no obvious defects in neural tube closure and/or body laterality. Instead, Cobl knock out mice were reported to show defects in the inner ear suggesting a role of Cobl in postnatal planar cell polarity refinements and in the organization of the sensory structures in the cochlea. In line, Cobl KO mice showed defects in cochlear amplification.[16] Zebra fish deficient for Cobl showed severe defects in body laterality and balance keeping.[15]

## Comparison with Spire and Arp2/3 complex

[edit]

Several actin nucleators are present in mammalian cells. Cobl, Spire and Leiomodin form one group of such proteins because of their molecular mechanisms of actin nucleation all critically require their WH2 domain(s) - a common motif found in all of these nucleators.[12] Other protein containing WH2 domain have other functions. And other nucleators, such as formins, nucleate actin filaments using a different actin-binding motif, e.g. the FH2 (formin homology 2) domain.

Cordon-bleu protein, uses two WH2 motifs (blue segment) for the recruitment of ATP-actin monomers (dark orange) to form a linear actin dimer (Fig. 3). A short linker (short green segment) permits a close association between the linearly arranged actin subunits; a longer linker (long green segment) permits a third ATP-actin monomer to bind to the most carboxy-terminal WH2 motif to assemble in a cross-filament orientation, creating a trimeric actin nucleus.[22][12]

In contrast, Spire, which contains four closely spaced WH2s, is proposed to nucleate actin filaments by stabilizing the association of four actin monomers along a single, linear strand. Additional four ATP-actin monomers associate laterally along this tetramer to form a short typical two-strand helical actin filament (cf. Fig. 2C).

In the case of the WASp-Arp2/3-complex, WASp (yellow segment, Fig. 3) binds to and activates the Arp2/3 complex (purple structures, the nucleator complex) by orienting the two ARP subunits in a conformation similar to the barbed end of an actin filament. The WH2 motif in WASp recruits ATP-G-actin that binds to either Arp2 or Arp3 to complete the formation of a trimeric actin nucleus.[22]

## References

[edit]

1. ^ a b c GRCh38: Ensembl release 89: ENSG00000106078 - Ensembl, May 2017
2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020173 - Ensembl, May 2017
3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. ^ a b c d e f g h i j k l m Ahuja R, Pinyol R, Reichenbach N, Custer L, Klingensmith J, Kessels MM, Qualmann B (October 2007). "Cordon-bleu is an actin nucleation factor and controls neuronal morphology". Cell. 131 (2): 337–50\. doi:10.1016/j.cell.2007.08.030. PMC 2507594. PMID 17956734.
6. ^ a b c d Schwintzer L, Koch N, Ahuja R, Grimm J, Kessels MM, Qualmann B (July 2011). "The functions of the actin nucleator Cobl in cellular morphogenesis critically depend on syndapin I". The EMBO Journal. 30 (15): 3147–59\. doi:10.1038/emboj.2011.207. PMC 3160182. PMID 21725280.
7. ^ a b c d e f g Haag N, Schwintzer L, Ahuja R, Koch N, Grimm J, Heuer H, Qualmann B, Kessels MM (December 2012). "The actin nucleator Cobl is crucial for Purkinje cell development and works in close conjunction with the F-actin binding protein Abp1". The Journal of Neuroscience. 32 (49): 17842–56\. doi:10.1523/JNEUROSCI.0843-12.2012. PMC 6621670. PMID 23223303.
8. ^ a b c d e f Hou W, Izadi M, Nemitz S, Haag N, Kessels MM, Qualmann B (2015). "The Actin Nucleator Cobl Is Controlled by Calcium and Calmodulin". PLOS Biology. 13 (9): e1002233. doi:10.1371/journal.pbio.1002233. PMC 4559358. PMID 26334624.
9. ^ a b c d e Hou W, Nemitz S, Schopper S, Nielsen ML, Kessels MM, Qualmann B (April 2018). "Arginine Methylation by PRMT2 Controls the Functions of the Actin Nucleator Cobl". Developmental Cell. 45 (2): 262–275.e8. doi:10.1016/j.devcel.2018.03.007. PMID 29689199.
10. ^ a b c d e Gasca S, Hill DP, Klingensmith J, Rossant J (1995). "Characterization of a gene trap insertion into a novel gene, cordon-bleu, expressed in axial structures of the gastrulating mouse embryo". Developmental Genetics. 17 (2): 141–54\. doi:10.1002/dvg.1020170206. PMID 7586755.
11. ^ Chesarone MA, Goode BL (February 2009). "Actin nucleation and elongation factors: mechanisms and interplay". Review. Current Opinion in Cell Biology. 21 (1): 28–37\. doi:10.1016/j.ceb.2008.12.001. PMC 2671392. PMID 19168341.
12. ^ a b c Qualmann B, Kessels MM (June 2009). "New players in actin polymerization--WH2-domain-containing actin nucleators". Review. Trends in Cell Biology. 19 (6): 276–85\. doi:10.1016/j.tcb.2009.03.004. PMID 19406642.
13. ^ a b Renault L, Bugyi B, Carlier MF (October 2008). "Spire and Cordon-bleu: multifunctional regulators of actin dynamics". Review. Trends in Cell Biology. 18 (10): 494–504\. doi:10.1016/j.tcb.2008.07.008. PMID 18774717.
14. ^ Kessels MM, Engqvist-Goldstein AE, Drubin DG (January 2000). "Association of mouse actin-binding protein 1 (mAbp1/SH3P7), an Src kinase target, with dynamic regions of the cortical actin cytoskeleton in response to Rac1 activation". Molecular Biology of the Cell. 11 (1): 393–412\. doi:10.1091/mbc.11.1.393. PMC 14781. PMID 10637315.
15. ^ a b c Schüler S, Hauptmann J, Perner B, Kessels MM, Englert C, Qualmann B (January 2013). "Ciliated sensory hair cell formation and function require the F-BAR protein syndapin I and the WH2 domain-based actin nucleator Cobl". Journal of Cell Science. 126 (Pt 1): 196–208\. doi:10.1242/jcs.111674. PMID 23203810.
16. ^ a b c Haag N, Schüler S, Nietzsche S, Hübner CA, Strenzke N, Qualmann B, Kessels MM (August 2018). "The Actin Nucleator Cobl Is Critical for Centriolar Positioning, Postnatal Planar Cell Polarity Refinement, and Function of the Cochlea". Cell Reports. 24 (9): 2418–2431.e6. doi:10.1016/j.celrep.2018.07.087. PMID 30157434.
17. ^ Izadi M, Schlobinski D, Lahr M, Schwintzer L, Qualmann B, Kessels MM (January 2018). "Cobl-like promotes actin filament formation and dendritic branching using only a single WH2 domain". The Journal of Cell Biology. 217 (1): 211–230\. doi:10.1083/jcb.201704071. PMC 5748978. PMID 29233863.
18. ^ Paunola E, Mattila PK, Lappalainen P (February 2002). "WH2 domain: a small, versatile adapter for actin monomers". FEBS Letters. 513 (1): 92–7\. Bibcode:2002FEBSL.513...92P. doi:10.1016/S0014-5793(01)03242-2. PMID 11911886. S2CID 5914765.
19. ^ "WH2 domain (IPR003124)". InterPro.
20. ^ Quinlan ME, Heuser JE, Kerkhoff E, Mullins RD (January 2005). "Drosophila Spire is an actin nucleation factor". Nature. 433 (7024): 382–8\. Bibcode:2005Natur.433..382Q. doi:10.1038/nature03241. PMID 15674283. S2CID 4424757.
21. ^ Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE (December 2002). "DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed". Mammalian Genome. 13 (12): 686–91\. doi:10.1007/s00335-002-3028-z. PMID 12514746. S2CID 361009.
22. ^ a b Winckler B, Schafer DA (October 2007). "Cordon-bleu: a new taste in actin nucleation". Cell. 131 (2): 236–8\. doi:10.1016/j.cell.2007.10.003. PMID 17956726. S2CID 15489368.