DAAM1

DAAM1
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2J1D, 2Z6E
Identifiers
Aliases	DAAM1, dishevelled associated activator of morphogenesis 1
External IDs	OMIM: 606626 MGI: 1914596 HomoloGene: 36635 GeneCards: DAAM1
Gene location (Human)
Chr.	Chromosome 14 (human)[1]
End	59,371,405 bp[1]
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)[2]
End	71,992,333 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• Rho GTPase binding; • actin binding; • GO:0001948 protein binding; • identical protein binding;
Cellular component	• cell membrane; • membrane; • stress fiber; • ciliary basal body; • motile cilium; • cytoplasm; • cytosol; • cytoskeleton; • cell projection;
Biological process	• actin cytoskeleton organization; • cellular component organization; • Wnt signaling pathway, planar cell polarity pathway; • Wnt signaling pathway;
	Sources:Amigo / QuickGO
Orthologs
	23002
	208846
	ENSG00000100592
	ENSMUSG00000034574
	Q9Y4D1
	Q8BPM0
	NM_001270520; NM_014992
	NM_001286452; NM_026102; NM_172464
	NP_001257449; NP_055807
	NP_001273381; NP_080378; NP_766052
	Wikidata
View/Edit Human	View/Edit Mouse

Disheveled-associated activator of morphogenesis 1 is a protein that in humans is encoded by the DAAM1 gene.[5][6][7] Evidence of alternative splicing has been observed for this gene but the full-length nature of these variants has not been determined.

Function

Cell motility, adhesion, and cytokinesis, and other functions of the cell cortex are mediated by the reorganization of the actin cytoskeleton and recent evidence suggests a role for formin homology (FH) proteins in these processes. The protein encoded by this gene contains FH domains and belongs to a novel FH protein subfamily implicated in cell polarity. Wnt/Fz signaling activates the small GTPase Rho, a key regulator of cytoskeleton architecture, to control cell polarity and movement during development. Activation requires Dvl-Rho complex formation, an assembly mediated by this gene product, which is thought to function as a scaffolding protein.[7]

Clinical significance

The deletion of a single copy of this gene has been associated with congenital heart defects.[8]

References

GRCh38: Ensembl release 89: ENSG00000100592 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000034574 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Habas R, Kato Y, He X (Jan 2002). "Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1". Cell. 107 (7): 843–54. doi:10.1016/S0092-8674(01)00614-6. PMID 11779461.
Liu W, Sato A, Khadka D, Bharti R, Diaz H, Runnels LW, Habas R (Jan 2008). "Mechanism of activation of the Formin protein Daam1". Proc Natl Acad Sci U S A. 105 (1): 210–5. doi:10.1073/pnas.0707277105. PMC 2224188. PMID 18162551.
"Entrez Gene: DAAM1 dishevelled associated activator of morphogenesis 1".
Bao B, Zhang L, Hu H, Yin S, Liang Z (August 2012). "Deletion of a single-copy DAAM1 gene in congenital heart defect: a case report". BMC Med. Genet. 13 (1): 63. doi:10.1186/1471-2350-13-63. PMC 3482563. PMID 22857009.

Tanaka K (2000). "Formin family proteins in cytoskeletal control". Biochem. Biophys. Res. Commun. 267 (2): 479–81. doi:10.1006/bbrc.1999.1707. PMID 10631086.
Ishikawa K, Nagase T, Suyama M, et al. (1998). "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Res. 5 (3): 169–76. doi:10.1093/dnares/5.3.169. PMID 9734811.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Heilig R, Eckenberg R, Petit JL, et al. (2003). "The DNA sequence and analysis of human chromosome 14". Nature. 421 (6923): 601–7. doi:10.1038/nature01348. PMID 12508121.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Aspenström P, Richnau N, Johansson AS (2006). "The diaphanous-related formin DAAM1 collaborates with the Rho GTPases RhoA and Cdc42, CIP4 and Src in regulating cell morphogenesis and actin dynamics". Exp. Cell Res. 312 (12): 2180–94. doi:10.1016/j.yexcr.2006.03.013. PMID 16630611.
Sato A, Khadka DK, Liu W, et al. (2007). "Profilin is an effector for Daam1 in non-canonical Wnt signaling and is required for vertebrate gastrulation". Development. 133 (21): 4219–31. doi:10.1242/dev.02590. PMID 17021034.
Lu J, Meng W, Poy F, et al. (2007). "Structure of the FH2 domain of Daam1: implications for formin regulation of actin assembly". J. Mol. Biol. 369 (5): 1258–69. doi:10.1016/j.jmb.2007.04.002. PMC 1939941. PMID 17482208.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000100592 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000034574 - 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.

[pmid11779461-5] Habas R, Kato Y, He X (Jan 2002). "Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1". Cell. 107 (7): 843–54. doi:10.1016/S0092-8674(01)00614-6. PMID 11779461.

[pmid18162551-6] Liu W, Sato A, Khadka D, Bharti R, Diaz H, Runnels LW, Habas R (Jan 2008). "Mechanism of activation of the Formin protein Daam1". Proc Natl Acad Sci U S A. 105 (1): 210–5. doi:10.1073/pnas.0707277105. PMC 2224188. PMID 18162551.

[entrez-7] "Entrez Gene: DAAM1 dishevelled associated activator of morphogenesis 1".

[pmid22857009-8] Bao B, Zhang L, Hu H, Yin S, Liang Z (August 2012). "Deletion of a single-copy DAAM1 gene in congenital heart defect: a case report". BMC Med. Genet. 13 (1): 63. doi:10.1186/1471-2350-13-63. PMC 3482563. PMID 22857009.

DAAM1

Function

Clinical significance

References

Further reading