Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-8-235
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dc.titleThe 10 sea urchin receptor for egg jelly proteins (SpREJ) are members of the polycystic kidney disease-1 (PKD1) family.
dc.contributor.authorGunaratne, H.J
dc.contributor.authorMoy, G.W
dc.contributor.authorKinukawa, M
dc.contributor.authorMiyata, S
dc.contributor.authorMah, S.A
dc.contributor.authorVacquier, V.D
dc.date.accessioned2020-10-20T04:48:32Z
dc.date.available2020-10-20T04:48:32Z
dc.date.issued2007
dc.identifier.citationGunaratne, H.J, Moy, G.W, Kinukawa, M, Miyata, S, Mah, S.A, Vacquier, V.D (2007). The 10 sea urchin receptor for egg jelly proteins (SpREJ) are members of the polycystic kidney disease-1 (PKD1) family.. BMC genomics 8 : 235. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-8-235
dc.identifier.issn14712164
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178005
dc.description.abstractBACKGROUND: Mutations in the human polycystic kidney disease-1 (hPKD1) gene result in ~85% of cases of autosomal dominant polycystic kidney disease, the most frequent human monogenic disease. PKD1 proteins are large multidomain proteins involved in a variety of signal transduction mechanisms. Obtaining more information about members of the PKD1 family will help to clarify their functions. Humans have five hPKD1 proteins, whereas sea urchins have 10. The PKD1 proteins of the sea urchin, Strongylocentrotus purpuratus, are referred to as the Receptor for Egg Jelly, or SpREJ proteins. The SpREJ proteins form a subfamily within the PKD1 family. They frequently contain C-type lectin domains, PKD repeats, a REJ domain, a GPS domain, a PLAT/LH2 domain, 1-11 transmembrane segments and a C-terminal coiled-coil domain. RESULTS: The 10 full-length SpREJ cDNA sequences were determined. The secondary structures of their deduced proteins were predicted and compared to the five human hPKD1 proteins. The genomic structures of the 10 SpREJs show low similarity to each other. All 10 SpREJs are transcribed in either embryos or adult tissues. SpREJs show distinct patterns of expression during embryogenesis. Adult tissues show tissue-specific patterns of SpREJ expression. CONCLUSION: Possession of a REJ domain of about 600 residues defines this family. Except for SpREJ1 and 3, that are thought to be associated with the sperm acrosome reaction, the functions of the other SpREJ proteins remain unknown. The sea urchin genome is one-fourth the size of the human genome, but sea urchins have 10 SpREJ proteins, whereas humans have five. Determination of the tissue specific function of each of these proteins will be of interest to those studying echinoderm development. Sea urchins are basal deuterostomes, the line of evolution leading to the vertebrates. The study of individual PKD1 proteins will increase our knowledge of the importance of this gene family.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcomplementary DNA
dc.subjectegg protein
dc.subjectpolycystic kidney disease 1 protein
dc.subjectpolycystin
dc.subjectunclassified drug
dc.subjectanimal
dc.subjectarticle
dc.subjectbiological model
dc.subjectchemistry
dc.subjectDNA sequence
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjecthuman
dc.subjectmetabolism
dc.subjectmolecular cloning
dc.subjectmultigene family
dc.subjectmutation
dc.subjectprotein secondary structure
dc.subjectprotein tertiary structure
dc.subjectsea urchin
dc.subjecttissue distribution
dc.subjectAnimals
dc.subjectCloning, Molecular
dc.subjectDNA, Complementary
dc.subjectEgg Proteins
dc.subjectGene Expression Regulation
dc.subjectHumans
dc.subjectModels, Genetic
dc.subjectMultigene Family
dc.subjectMutation
dc.subjectProtein Structure, Secondary
dc.subjectProtein Structure, Tertiary
dc.subjectSea Urchins
dc.subjectSequence Analysis, DNA
dc.subjectTissue Distribution
dc.subjectTRPP Cation Channels
dc.typeArticle
dc.contributor.departmentANATOMY
dc.description.doi10.1186/1471-2164-8-235
dc.description.sourcetitleBMC genomics
dc.description.volume8
dc.description.page235
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