{{Short description|Protein-coding gene in the species Homo sapiens}} {{cs1 config|name-list-style=vanc}} {{Infobox_gene}}
''Megf8'' also known as '''Multiple Epidermal Growth Factor-like Domains 8''', is a protein coding gene that encodes a single pass membrane protein, known to participate in developmental regulation and cellular communication.<ref name="Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy">{{cite journal | vauthors = Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, Gunn TM, Kramer KL, De Jong PJ, Pennacchio LA, Lo CW | title = Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 106 | issue = 9 | pages = 3219–24 | date = March 2009 | pmid = 19218456 | pmc = 2651267 | doi = 10.1073/pnas.0813400106 | bibcode = 2009PNAS..106.3219Z | doi-access = free }}</ref> It is located on chromosome 19 at the 49th open reading frame in humans (19q13.2).<ref name=GeneCard-MEGF8>{{cite web|title=Multiple Epidermal Growth Factor-like Domains 8 Gene|url=https://www.genecards.org/cgi-bin/carddisp.pl?gene=MEGF8|work=MEGF8 Gene Card|publisher=Weizmann Institute of Science in Israel|access-date=4 February 2014}}</ref> There are two isoform constructs known for MEGF8, which differ by a 67 amino acid indel. The isoform 2 splice version (analyzed throughout this page) is 2785 amino acids long, and predicted to be 296.6 kdal in mass. Isoform 1 is composed of 2845 amino acids and predicted to weigh 303.1 kdal. Using BLAST searches, orthologs were found primarily in mammals, but MEGF8 is also conserved in invertebrates and fishes, and rarely in birds, reptiles, and amphibians. A notably important paralog to multiple epidermal growth factor-like domains 8 is ATRNL1 (Attractin-like 1), which is also a single pass transmembrane protein, with several of the same key features and motifs as MEGF8, as indicated by Simple Modular Architecture Research Tool<ref name="Proc. Natl. Acad. Sci. U.S.A.">{{cite journal | vauthors = Schultz J, Milpetz F, Bork P, Ponting CP | title = SMART, a simple modular architecture research tool: identification of signaling domains | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 95 | issue = 11 | pages = 5857–64 | date = May 1998 | pmid = 9600884 | pmc = 34487 | doi = 10.1073/pnas.95.11.5857 | bibcode = 1998PNAS...95.5857S | doi-access = free }}</ref> (SMART) which is hosted by the European Molecular Biology Laboratory located in Heidelberg, Germany. MEGF8 has been predicted to be a key player in several developmental processes, such as left-right patterning and limb formation. Currently, researchers have found MEGF8 SNP mutations to be the cause of Carpenter syndrome subtype 2.
==Gene==
=== Evolution & Orthologs=== A fairly highly conserved protein, MEGF8 has conserved orthologs from P. paniscus to N. vectensis. Orthologs are found in mammals, amphibians, fish, insects, crustaceans, and invertebrates.<ref name=Orthologs>{{cite web |title= BLAST |url= https://blast.ncbi.nlm.nih.gov/Blast.cgi | access-date = 8 March 2014}}</ref> Organization of the data showed that as time since divergence between humans and orthologs increased, the sequence identity decreased. {| border="1" |+ '''Table 1: MEGF8 Orthologs''' |-style="background:#F5FFFA;" |'''Genus/Species'''||'''Organism Common Name'''||'''Accession Number'''||'''Sequence Identity'''||'''Sequence Similarity'''||'''Length (AAs)''' |- style="background:#FFC1CC;" | Pan Paniscus||Pygmy Chimpanzee||XP_003811808 ||99%||99%||2778 |- style="background:#FFC1CC;" | Bos Mutus||Yak||XP_005909034||79%||82% ||2842 |- style="background:#FFC1CC;" | Orcinius Orca||Orca Whale||XP_004271289||93%||94%||2789 |- style="background:#FFC1CC;" | Trichechus manatus latirostris||Florida Manatee||XP_004388865||88%||89% ||2708 |- style="background:#FFC1CC;" | Leptonychotes weddellii||Weddell Seal||XP_006748348||91%||92% ||2068 |- style="background:#FFC1CC;" | Rattus norvegicus||Rat||NP_446080.1||88%||89% ||2789 |- style="background:#FFC1CC;" | Mus musculus||Mouse||NP_001153872.1||89%||90% ||2789 |- style="background:#F7E98E;" | Ophiophagus hannah||King Cobra||ETE71721||63%||70% ||404 |- style="background:#F7E98E;" | Alligator mississippiensis||American Alligator||XP_006273703||63%||71% ||2793 |- style="background:#F7E98E;" | Alligator sinensis||Chinese alligator||XP_006038171||67%||75% ||2465 |- style="background:#7FFFD4;" | Xenopus tropicalis||Western clawed frog||XP_002936442||56%||67% ||2730 |- style="background:#00BFFF;" | Neolamprologus brichardi||African Cichlid||XP_006808273||55%||67% ||2813 |- style="background:#00BFFF;" | Danio rerio||Zebra fish||XP_005158088||54%||66% ||2870 |- style="background:#00BFFF;" | IIctalurus punctatus||Channel Catfish||AHI50432||54%||77% ||2875 |- style="background:#00BFFF;" | Oryzias latipes||Japanese Rice Fish||XP_004078282||54%||67% ||2952 |- style="background:#CCCCFF;" | Apis mellifera||Western Honey Bee||XP_006568067||31%||45%||2913 |- style="background:#CCCCFF;" | Ceratitis capitata||Mediterranean Fruit Fly||JAB95791||32%||45%||2959 |- style="background:#D8BFD8;" | Daphnia pulex||Common Water Flea||EFX84934||35%||48%||2888 |- style="background:#6699CC;" | Strongylocentrotus purpuratus||Purple Sea Urchin||XP_789561||37%||51% ||194 |- style="background:#6699CC;" | Nematostella vectensis||Starlet Sea Anemone||XP_001635521||38%||51%||2534 |}
===Paralogs=== MEGF8 has one known paralog: ATRNL1. The ATRNL1 protein is approximately half the length of MEGF8, and contains several of the same conserved domains, including the CUB domain and transmembrane sequence. ATRNL1 is found in many birds and amphibians, where MEGF8 is not found in any birds, and only one amphibian.
===Promoters=== Genomatix's ElDorado (http://www.genomatix.de/ {{Webarchive|url=https://web.archive.org/web/20211202010908/https://www.genomatix.de/ |date=2021-12-02 }}), a gene promoter database, predicted ten different possible promoters for ''megf8.'' The promoter having promoter ID number GXP_1262882 and transcript ID GXT_22531930, was predicted with the highest confidence. This promoter is located on the plus strand of chromosome 19, ranging from nucleotide 42829077 to 42830497, making it a 1421 nucleotide long sequence. The promoter sequence overlaps with the transcriptional start codon in the gene.
===Transcription Factors=== More than one hundred transcription factor binding sites were predicted to be found in the ''megf8'' promoter region through Genomatix. The top twenty most confidently predicted factors include the following:
{{columns-list|colwidth=22em| * Ccaat/Enhancer Binding Protein * Vertebrate TATA binding protein factor * CCAAT binding factors * Activator-, mediator- and TBP-dependent core promoter element for RNA polymerase II transcription from TATA-less promoters * Chorion-specific transcription factors with a GCM DNA binding domain *Signal transducer and activator of transcription *Heat shock factors (2 sites) *GC-Box factors SP1/GC *Estrogen response elements *KRAB domain zinc finger protein 57 *Neuron-specific olfactory factor (2 sites) *Nuclear respiratory factor 1 *RXR heterodimer binding sites *GATA binding factors *Nuclear receptor subfamily 2 factors *Octamer binding protein *EGR/nerve growth factor induced protein C & related factors *Neuron-restrictive silencer factor }}
== Protein Architecture ==
===Primary Structure===
MEGF8 is composed of either 2845 amino acids (Isoform 1) or 2778 amino acids (Isoform 2). Isoform 2 undergoes a 67 amino acid removal from 700-766, which accounts for its shortened length; otherwise, the two isoforms are identical. Using SAPS, a Statistical Analysis of Protein Sequence <ref>{{cite web|last=Brendel|first=Volker|title=Statistical Analysis of PS|url=http://seqtool.sdsc.edu/CGI/BW.cgi#!|work=SAPS|publisher=Department of Mathematics, Stanford University|access-date=27 April 2014}}{{dead link|date=February 2018 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> software, amino acid bias was able to be determined. Isoform one is rich in cysteine and glycine, and deficient in isoleucine and lysine. Isoform 2 of MEGF8 was found to have very high levels of cysteine, moderately high levels of glycine, and low levels of isoleucine and lysine. The high levels of cysteine residues contributes to the numerous disulfide bonds found in the mature protein's folded structure. Overall, MEGF8 has a pH between 6.4 and 7.0, depending on the organism's sequence. Human MEGF8's pH is 6.4. This nearly neutral pH enables the protein to fold properly and inhibits denaturation. The twenty most conserved amino acids, found through a multiple sequence alignment of 20 orthologs, were found to be located in the CUB and transmembrane domains.
===Secondary Structure===
Prediction software PELE<ref>{{cite web|last=Pappas Jr..|first=Georgios J.|title=PELE-Protein Structure Prediction|url=http://seqtool.sdsc.edu/CGI/BW.cgi#!|publisher=SDSC Biology Workbench|access-date=24 April 2014}}{{dead link|date=February 2018 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> from UCSC Biology Workbench indicated that MEGF8 is primarily composed of beta-folded sheets, with occasional short alpha helix segments. PELE uses eight different prediction programs to compare and confirm predictions, enhancing the confidence level. The beta-folded sheets occur at many of the key domains, including the EGF-domains, kelch domains, and EGF-laminin domains. This information from PELE also corresponded with the secondary structure and 3D structure predictions made by PHYRE2<ref>{{cite journal|title=Protein structure prediction on the web: a case study using the Phyre server|url=http://www.sbg.bio.ic.ac.uk/phyre2/html/page.cgi?id=index|access-date=27 April 2014|vauthors=Kelley LA, Sternberg MJ | journal=Nature Protocols | author-link=Nature Protocols|pages=363–371|date=26 February 2009| volume=4 | issue=3 | doi=10.1038/nprot.2009.2 | pmid=19247286 | hdl=10044/1/18157 | hdl-access=free }}</ref>
=== Predicted Key Domains & Features ===
MEGF8 is predicted to contain several different types of features, domains, and motifs that play a key role in the protein's function, structure, and location. These are listed in Table 1. Functions, found through SMART<ref name="Proc. Natl. Acad. Sci. U.S.A."/> analysis, as well as NCBI Conserved Domains Search<ref name="NCBI">{{cite journal |vauthors=Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, DeWeese-Scott C, Fong JH, Geer LY, Geer RC, Gonzales NR, Gwadz M, Hurwitz DI, Jackson JD, Ke Z, Lanczycki CJ, Lu F, Marchler GH, Mullokandov M, Omelchenko MV, Robertson CL, Song JS, Thanki N, Yamashita RA, Zhang D, Zhang N, Zheng C, Bryant SH |title=CDD: a Conserved Domain Database for the functional annotation of proteins |journal=Nucleic Acids Research |volume=39 |issue=Database issue |pages=D225–9 |date=January 2011 |pmid=21109532 |pmc=3013737 |doi=10.1093/nar/gkq1189 |url=https://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi?INPUT_TYPE=live&SEQUENCE=BAA32469.2 }}</ref> include: *CUB domain: extracellular domain: present in proteins mostly known to be involved in development. *Epidermal Growth Factor Domain: a short peptide with a distinctive motif of six cysteines, which is found in many different proteins of diverse functions<ref name=PubMed>{{cite journal |vauthors=Davis CG |title=The many faces of epidermal growth factor repeats |journal=The New Biologist |volume=2 |issue=5 |pages=410–9 |date=May 1990 |pmid=2288911}}</ref> *EGF-like domain: contains several sub-families of different functions according to location and protein; not specified for MEGF8. *Calcium EGF-like domain: Calcium-binding EGF-like domain, present in a large number of membrane-bound and extracellular (mostly animal) proteins. Many of these proteins require calcium for their biological function and calcium-binding sites have been found to be located at the N-terminus of particular EGF-like domains. *Kelch motif: Galactose oxidase, central domain; Found to cause formation of ß propeller tertiary structure of the protein. *Leucine Zipper: A motif found in regulatory proteins, as predicted by PSORT II<ref>{{cite journal | vauthors = Nakai K, Horton P | title = PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization | journal = Trends in Biochemical Sciences | volume = 24 | issue = 1 | pages = 34–6 | date = January 1999 | pmid = 10087920 | doi = 10.1016/S0968-0004(98)01336-X }}</ref> *Laminin EGF-like domain: laminins are the major noncollagenous components of basement membranes that mediate cell adhesion, growth migration, and differentiation; the laminin-type epidermal growth factor-like module occurs in tandem arrays; the domain contains 4 disulfide bonds (loops a-d) the first three resemble epidermal growth factor (EGF). *PSI domain: domain found in plexins, semaphorins and integrins. Plexin are involved in the development of neural and epithelial tissues; semaphorins induce the collapse and paralysis of neuronal growth cones; and integrins may mediate adhesive or migratory functions of epithelial cells.
====Predicted Domain & Motif Locations====
{| border="1" |+ '''Table 2: Predicted Key Features, Domains, & Motifs Found in MEGF8 Human Protein''' <small><br /> Found through the use of Simple Modular Architecture Research Tool for the Human MEGF8 Sequence, with the NCBI accession number BAA32469.2. </small> |-style="background:#F5FFFA;" | ''''' Feature, Domain, or Motif Name ''''' || ''''' Number in MEGF8''''' || '''''Amino Acid Location Range (1-2785)''''' |- | Signal Peptide || 1 || 1-34 |- | CUB Domain || 1 ||40-147 |- | Epidermal Growth Factor (EGF) Domain || 6 || 148-177; 180-210; 1057-1100; 2121-2160; 2162-2190; 2200-2240 |- | D1k3ia Structural Domain || 2 || 233-550; 1449-1801 |- | Kelch Repeat || 9 || 241-276; 340-388; 454-504; 519-575; 1450-1492; 1505-1552; 1724-1764; 1780-1820; 2239-2255 |- |Leucine Zipper Pattern || 1 || 1698-1719 |- | PSI Domain || 6 || 787-839; 889-931; 945-1013; 1864-1919; 2008-2058; 2060-2117 |- | EGF_Ca Domain || 1 || 1014-1055 |- | EGF_Like Domain || 4 || 1103-1148; 1346-1485; 2244-2317; 2320-2381 |- | EGF_LAM Domain || 1 || 1151-1199 |- | Transmembrane Region || 1 || 2588-2610 |}
thumb|center | 1150x1100px |Scaled Map of MEGF8 Features along protein
thumb|center | 550x500px | Human ATRNL1 (Paralog to MEGF8) Protein Feature Map
===Tertiary Structure=== One of the key attributes of MEGF8's tertiary structure is its 7-bladed beta propeller which is formed by the kelch motif found in its D1k3ia3 structural domain, which was identified by SCOP. SCOP<ref name="pmid18000004">{{cite journal | vauthors = Andreeva A, Howorth D, Chandonia JM, Brenner SE, Hubbard TJ, Chothia C, Murzin AG | title = Data growth and its impact on the SCOP database: new developments | journal = Nucleic Acids Research | volume = 36 | issue = Database issue | pages = D419–25 | year = 2008 | pmid = 18000004 | pmc = 2238974 | doi = 10.1093/nar/gkm993 }}</ref> also indicated that the beta-propeller in MEGF8 is a member of the galactose oxidase super family. Each of the seven blades are made up of a four stranded beta-folded motifs. It is also important to note that although many phosphorylation sites are predicted at high confidence, several other topographic predictions (i.e. disulfide bonds, glycosylation, other extracellular features), do not support these predictions.
==== Predicted Post Translational Modifications ==== {| border="1" |+ '''Table 3: Key Predicted Post Translational Modifications Found in MEGF8 Human Protein''' |-style="background:#F5FFFA;" | ''''' Feature ''''' || ''''' Number Predicted in MEGF8''''' || '''''Amino Acid Location Range (1-2785)''''' || '''''Source''''' |- | Cysteine involved in Disulfide Bond || 99+ Possible Sites || - || DISULFIND<ref>{{cite journal | vauthors = Ceroni A, Passerini A, Vullo A, Frasconi P | title = DISULFIND: a disulfide bonding state and cysteine connectivity prediction server | journal = Nucleic Acids Research | volume = 34 | issue = Web Server issue | pages = W177–81 | date = July 2006 | pmid = 16844986 | pmc = 1538823 | doi = 10.1093/nar/gkl266 }}</ref> & UniProt |- | SUMOylation || 3 (confidently) || K886; K1681; K1737 || SUMOplot<ref>{{cite journal|last=Gramatikoff|first=Kosi|title=In Frontiers of Biotechnology and Pharmaceuticals|journal=Science Press|date=2004|issue=4|page=181|display-authors=etal}}</ref> |- | Phosphorylation || 116 || - || NetPhos<ref>{{cite journal | vauthors = Blom N, Gammeltoft S, Brunak S | title = Sequence and structure-based prediction of eukaryotic protein phosphorylation sites | journal = Journal of Molecular Biology | volume = 294 | issue = 5 | pages = 1351–62 | date = December 1999 | pmid = 10600390 | doi = 10.1006/jmbi.1999.3310 }}</ref> |- | Internal Repeats || 1 || CQCNGH 1144-1149 & 2313-2318 || SAPS<ref name="pmid7583634">{{cite journal | vauthors = Karlin S | title = Statistical significance of sequence patterns in proteins | journal = Current Opinion in Structural Biology | volume = 5 | issue = 3 | pages = 360–71 | date = June 1995 | pmid = 7583634 | doi = 10.1016/0959-440X(95)80098-0 }}</ref> |- | N-linked Glycosylation || 20 || 56; 223; 267; 427; 699; 749; 968; 987; 1054; 1140; 1210; 1539; 1908; 1929; 2006; 2153; 2168; 2340; 2778 || NetNGlyc<ref>{{cite journal | vauthors = Blom N, Sicheritz-Pontén T, Gupta R, Gammeltoft S, Brunak S | title = Prediction of post-translational glycosylation and phosphorylation of proteins from the amino acid sequence | journal = Proteomics | volume = 4 | issue = 6 | pages = 1633–49 | date = June 2004 | pmid = 15174133 | doi = 10.1002/pmic.200300771 | s2cid = 18810164 | url = http://orbit.dtu.dk/en/publications/prediction-of-posttranslational-glycosylation-and-phosphorylation-of-proteins-from-the-amino-acid-sequence(f32116cb-58e4-4fb8-b130-d22328e8e5e4).html | url-access = subscription }}</ref> |- | Signal Peptide Cleavage || 1 || between amino acids 34 and 35 || SignalP<ref>{{cite journal | vauthors = Bendtsen JD, Nielsen H, von Heijne G, Brunak S | title = Improved prediction of signal peptides: SignalP 3.0 | journal = Journal of Molecular Biology | volume = 340 | issue = 4 | pages = 783–95 | date = July 2004 | pmid = 15223320 | doi = 10.1016/j.jmb.2004.05.028 | citeseerx = 10.1.1.165.2784 }}</ref> |- | Hydrophobic Domain || 1 || 2588-2610 || SAPS |- | Extracellular Domain || 1 || 1- 2587 || Phobius<ref>{{cite journal | vauthors = Käll L, Krogh A, Sonnhammer EL | title = Advantages of combined transmembrane topology and signal peptide prediction--the Phobius web server | journal = Nucleic Acids Research | volume = 35 | issue = Web Server issue | pages = W429–32 | date = July 2007 | pmid = 17483518 | pmc = 1933244 | doi = 10.1093/nar/gkm256 }}</ref> |- | Transmembrane Region || 1 || 2588-2610 || Phobius, SAPS, SMART |- | Intracellular Domain || 1 || 2611-2785 || Phobius, SMART |}
==Expression== MEGF8 is found to be expressed at high levels in cardiac myocytes and fetal brain tissue, according to GeoProfiles,<ref>{{cite web|title=MEGF8 - Large-scale analysis of the human transcriptome (HG-U133A)|url=https://www.ncbi.nlm.nih.gov/geoprofiles/4694154|work=GeoProfiles|publisher=NCBI|access-date=15 April 2014}}</ref> from NCBI. This GeoProfile also indicated that MEGF8 was found to be at moderate to moderately low expression levels in all other tissues examined. NCBI GeoProfile data also provided the tissue expression graph for MEGF8 in humans, which is displayed to the right, further illustrating specific sites and levels of expression<ref>{{cite journal | vauthors = Barrett T, Troup DB, Wilhite SE, Ledoux P, Evangelista C, Kim IF, Tomashevsky M, Marshall KA, Phillippy KH, Sherman PM, Muertter RN, Holko M, Ayanbule O, Yefanov A, Soboleva A | title = NCBI GEO: archive for functional genomics data sets--10 years on | journal = Nucleic Acids Research | volume = 39 | issue = Database issue | pages = D1005–10 | date = January 2011 | pmid = 21097893 | pmc = 3013736 | doi = 10.1093/nar/gkq1184 }}</ref>
thumb|center | 1150x1100px| NCBI GeoProfile for MEGF8 Tissues Expression in Humans
===Function and Mechanisms in Cellular Processes===
====Molecular Function==== According to BioGPS<ref name="10.1186/gb-2009-10-11-r130">{{cite journal | vauthors = Wu C, Orozco C, Boyer J, Leglise M, Goodale J, Batalov S, Hodge CL, Haase J, Janes J, Huss JW, Su AI | title = BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources | journal = Genome Biology | volume = 10 | issue = 11 | article-number = R130 | date = 2009 | pmid = 19919682 | pmc = 3091323 | doi = 10.1186/gb-2009-10-11-r130 | doi-access = free }}</ref> gene ontology information, MEGF8 is an active participant in receptor activity, calcium ion binding, protein binding.
====Role in Biological Processes==== Analysis of gene ontology information by BioGPS<ref name="10.1186/gb-2009-10-11-r130" /> was able to produce a list of biological processes in each of which MEGF8 plays a significant role:
{{columns-list|colwidth=30em| *embryonic heart tube morphogenesis (GO:0003143) *regulation of gene expression (GO:0010468) *embryonic limb morphogenesis (GO:0030326) *BMP signaling pathway (GO:0030509) *limb morphogenesis (GO:0035108) *cell migration involved in gastrulation (GO:0042074) *embryonic skeletal system morphogenesis (GO:0048704) *positive regulation of axon extension involved in axon guidance (GO:0048842) *epiboly involved in gastrulation with mouth forming second (GO:0055113) *embryonic heart tube left/right pattern formation (GO:0060971) *left/right pattern formation (GO:0060972) *determination of heart left/right asymmetry (GO:0061371) *determination of digestive tract left/right asymmetry (GO:0071907) *craniofacial suture morphogenesis (GO:0097094) *fasciculation of sensory neuron axon (GO:0097155) }}
====Putative Interactions==== In the table below, all predicted interactions, except SMARCD3, are supported by two-hybrid screen experimental data. This information is supported by both NextProt<ref>{{cite journal | vauthors = Lane L, Argoud-Puy G, Britan A, Cusin I, Duek PD, Evalet O, Gateau A, Gaudet P, Gleizes A, Masselot A, Zwahlen C, Bairoch A | title = neXtProt: a knowledge platform for human proteins | journal = Nucleic Acids Research | volume = 40 | issue = Database issue | pages = D76–83 | date = January 2012 | pmid = 22139911 | pmc = 3245017 | doi = 10.1093/nar/gkr1179 }}</ref> database and IntAct database.<ref>{{cite journal | vauthors = Kerrien S, Aranda B, Breuza L, Bridge A, Broackes-Carter F, Chen C, Duesbury M, Dumousseau M, Feuermann M, Hinz U, Jandrasits C, Jimenez RC, Khadake J, Mahadevan U, Masson P, Pedruzzi I, Pfeiffenberger E, Porras P, Raghunath A, Roechert B, Orchard S, Hermjakob H | title = The IntAct molecular interaction database in 2012 | journal = Nucleic Acids Research | volume = 40 | issue = Database issue | pages = D841–6 | date = January 2012 | pmid = 22121220 | pmc = 3245075 | doi = 10.1093/nar/gkr1088 }}</ref> The two interactions with the highest confidence value are also supported by materials found by text-mining in STRING.<ref>{{cite journal | vauthors = Jensen LJ, Kuhn M, Stark M, Chaffron S, Creevey C, Muller J, Doerks T, Julien P, Roth A, Simonovic M, Bork P, von Mering C | title = STRING 8--a global view on proteins and their functional interactions in 630 organisms | journal = Nucleic Acids Research | volume = 37 | issue = Database issue | pages = D412–6 | date = January 2009 | pmid = 18940858 | pmc = 2686466 | doi = 10.1093/nar/gkn760 }}</ref> Together, it is with reasonably high confidence that the proteins in red are interacting with MEGF8, and with moderate confidence that the proteins in green interact with MEGF8. The confidence level for the proteins in blue is much lower, which may mean that the two-hybrid assay provided a false positive, or that they actually are interacting. {| border="1" |+<big> ''' Table 4: Putative Protein Interactions with Human MEGF8 ''' </big> |-style="background:#F5FFFA;" | ''''' Predicted Interacting Protein ''''' || ''''' Confidence''''' || '''''Location''''' || '''''Description''''' || '''''Experimental/Text Support''''' || '''''Function''''' || '''''Source''''' |- |<span style="color:red">GFI1B</span> || Conf:0.866 || Found in Endothelial & Erythroid || GFI1B is a growth factor independent 1B transcription repressor || Two-Hybrid (IntAct) Text-mining (STRING/OMIM) || Essential proto-oncogenic transcriptional regulator; Transcriptional repressor or activator depending on both promoter and cell type context; represses promoter activity of SOCS1 and SOCS3 and thus, may regulate cytokine signaling pathways. || IntAct, STRING, NextProt |- |<span style="color:#0f0">ATN1</span> || Conf: 0.538 || Everywhere ||Atrophin 1 (ATN1) || Two Hybrid Assay || Transcriptional corepressor. Recruits NR2E1 to repress transcription. Promotes vascular smooth cell (VSMC) migration and orientation || IntAct, STRING |- | <span style="color:#0f0">ATXN7</span> || Conf: 0.510 || Mod-High Everywhere || Apinocerebellar ataxia type 7 protein (ATXN7) || Two Hybrid, Pull-Down || Acts as component of the STAGA transcription coactivator-HAT complex. Mediates the interaction of STAGA complex with the CRX and is involved in CRX-dependent gene activation. Necessary for microtubule cytoskeleton stabilization || Int Act, NextProt |- | <span style="color:#0f0">CACNA1A</span> || Conf: 0.510 || Certain Brain Tissues || Calcium Channel, Voltage-Dependent, P/Q Type, Alpha 1A Subunit (Cav2.1)|| Two Hybrid Assay, Pull-Down || Mediates the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. || IntAct, NextProt |- | <span style="color:red"> SMARCD3 </span> || Conf: 0.778 || High Everywhere || SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member (SMARCD3)|| Text-mining (OMIM article for SMARCS3)|| Plays a role in ATP dependent nucleosome remodeling by SMARCA4 containing complexes. Stimulates nuclear receptor mediated transcription || STRING |- |<span style="color:#0000FF"> FIHB1</span> || Conf: 0.370 || || ||Two Hybrid Pooling || Uncharacterized || IntAct, NextProt |- | <span style="color:#0000FF"> Y3542</span>|| Conf: 0.370 || || (Q8CKF8 in UniProtKB) || Two Hybrid Pooling || Uncharacterized || IntAct, NextProt |- | <span style="color:#0000FF"> ProW</span>|| Conf: 0.370 || || || Two Hybrid Pooling || Uncharacterized || IntAct, NextProt | |}
==Alternative Splicing, Mutations, & Phenotypic Impacts==
===Splice Variants=== The four primary splice variants and their distinctions are described below (labels correspond to those in image below):
'''A:''' has spliced out Exon 13. Looking at the attached working conceptual translation, it can be seen that exon 3 does not code for any feature, domain, motif or other functional section of aa, and is likely therefore not key to the function of MEGF8 protein. This is the variant that corresponds to the splice model of the analyzed megf8.
'''B:''' Spliced out exons 1-6; these exons hold several key domains and motifs including the CUB domain, two PSI domains, a D1k3ia3 structural domain, and a kelch repeat. This may result in a misfolded protein without the structural segments, and inhibit participation in development events (loss of PSI and CUB). Still has signal and TMEM so may still be able to partially function
''' C:''' part of the D1k3ia3 structural domain remains in exon 29, but the kelch repeat has been excised, which could lead to structural issues. Also this variant contains almost 3 PSI domains, and an area of low complexity in exons 32-35, which may allow this variant to function in the cell, but no signal or TMEM to place in membrane so not a normal function
'''D:''' This variant is exons 36-40, excised 41, and a shortened 42 exon. It possesses EGF calcium domains and EGF/EGF-like domains. Loss of 41 will drastically alter the function as it possesses the TMEM segment. It depends on where 41 is lost and 42 is cleaved.
thumb|center| 750x700px |This diagram from AceView depicts the various forms of MEGF8 produced by alternative splicing
===Common Mutations===
====SNPs====
There are several SNPs, found through NCBI GeneView,<ref>{{cite journal | vauthors = Maglott D, Ostell J, Pruitt KD, Tatusova T | author-link1=Donna R. Maglott|title = Entrez Gene: gene-centered information at NCBI | journal = Nucleic Acids Research | volume = 39 | issue = Database issue | pages = D52–7 | date = January 2011 | pmid = 21115458 | pmc = 3013746 | doi = 10.1093/nar/gkq1237 }}</ref> that cause missense or silent mutations in MEGF8. However, three SNP mutations were identified as causes of Carpenter Syndrome 2 by Twigg et al.<ref name="10.1016/j.ajhg.2012.08.027">{{cite journal | vauthors = Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO | title = Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization | journal = American Journal of Human Genetics | volume = 91 | issue = 5 | pages = 897–905 | date = November 2012 | pmid = 23063620 | pmc = 3487118 | doi = 10.1016/j.ajhg.2012.08.027 }}</ref> The three SNP mutations are: Gly199 to Arg; Arg1499 to His; Ser2367 to Gly. The article by Twigg includes a supplementary data set that shows a multiple sequence alignment of the regions surrounding the SNPs and the domain in which the SNP lies. The Gly199 to Arg mutation is located inside an EGF-domain; the Arg1499 to His mutation is located within a kelch domain in the 7-bladed beta-sheet propeller; the Ser2367 to Gly is located within an EGF-Laminin domain. These domain are important to maintaining a properly folded protein and its function.
====Carpenter Syndrome 2==== Visit Carpenter syndrome for more extensive details related to the disease. Genetic mutations in MEGF8 have been found to be a principal cause of this rare genetic syndrome.
====Adverse Phenotypic Consequences==== Mutations in MEGF8 have been found to be linked to defective lateralization during development, as reported by Twigg et al.<ref name="10.1016/j.ajhg.2012.08.027" /> Common features of individuals with Carpenter Syndrome Subtype II include the following: {{columns-list|colwidth=30em| *Tower-shaped skull (craniosynostosis)<ref name="10.1002/ajmg.1320020210">{{cite journal | vauthors = Frias JL, Felman AH, Rosenbloom AL, Finkelstein SN, Hoyt WF, Hall BD | title = Normal intelligence in two children with Carpenter syndrome | journal = American Journal of Medical Genetics | volume = 2 | issue = 2 | pages = 191–9 | date = 1978 | pmid = 263437 | doi = 10.1002/ajmg.1320020210 }}</ref> *Intellectual disability<ref name="10.1002/ajmg.1320020210" /> *Polysyndactyly digits<ref name="10.1002/ajmg.1320020210" /> *High birth weight<ref name="pmid3322002">{{cite journal | vauthors = Cohen DM, Green JG, Miller J, Gorlin RJ, Reed JA | title = Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes | journal = American Journal of Medical Genetics | volume = 28 | issue = 2 | pages = 311–24 | date = October 1987 | pmid = 3322002 | doi = 10.1002/ajmg.1320280208 }}</ref> *Obesity in later life<ref name="pmid3322002" /> *congenital heart disease *Umbilical hernia<ref name="pmid3322002" /> *Cryptorchidism in males<ref name="pmid3322002" /> *Genu valgum ("knock-knee")<ref name="10.1016/j.ajhg.2012.08.027" /> }}
===Current Research=== There is no research being done currently to develop treatment or cures for Carpenter Syndrome 2. Researchers are still striving to understand the cause of the point mutations in MEGF8 that result in this extremely rare genetic disease.
== References == {{Reflist|33em}}
== Further reading == {{refbegin|33em}} * {{cite journal | vauthors = Victorine AS, Weida J, Hines KA, Robinson B, Torres-Martinez W, Weaver DD | title = Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactyly | journal = American Journal of Medical Genetics. Part A | volume = 164A | issue = 3 | pages = 820–3 | date = March 2014 | pmid = 24458945 | doi = 10.1002/ajmg.a.36362 | s2cid = 3040251 }} * {{cite journal | vauthors = Engelhard C, Sarsfield S, Merte J, Wang Q, Li P, Beppu H, Kolodkin AL, Sucov HM, Ginty DD | title = MEGF8 is a modifier of BMP signaling in trigeminal sensory neurons | journal = eLife | volume = 2 | article-number = e01160 | date = September 2013 | pmid = 24052814 | pmc = 3776557 | doi = 10.7554/eLife.01160 | doi-access = free }} * {{cite journal | vauthors = Nakayama M, Nakajima D, Nagase T, Nomura N, Seki N, Ohara O | title = Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening | journal = Genomics | volume = 51 | issue = 1 | pages = 27–34 | date = July 1998 | pmid = 9693030 | doi = 10.1006/geno.1998.5341 }} * {{cite journal | vauthors = Zhong J, Zou H | title = BMP signaling in axon regeneration | journal = Current Opinion in Neurobiology | volume = 27 | pages = 127–34 | date = August 2014 | pmid = 24713578 | doi = 10.1016/j.conb.2014.03.009 | pmc = 4122622 }} * {{cite journal | vauthors = Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO | title = Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization | journal = American Journal of Human Genetics | volume = 91 | issue = 5 | pages = 897–905 | date = November 2012 | pmid = 23063620 | pmc = 3487118 | doi = 10.1016/j.ajhg.2012.08.027 }} * {{cite journal | vauthors = Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, Gunn TM, Kramer KL, De Jong PJ, Pennacchio LA, Lo CW | title = Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 106 | issue = 9 | pages = 3219–24 | date = March 2009 | pmid = 19218456 | pmc = 2651267 | doi = 10.1073/pnas.0813400106 | bibcode = 2009PNAS..106.3219Z | doi-access = free }} {{refend}}
Category:Kelch proteins