Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2003-2-18
pubmed:abstractText
SPACRCAN is a novel proteoglycan present in the interphotoreceptor matrix (IPM) of the rat and human retina that resists aqueous extraction through its binding to hyaluronan. The purpose of this study was: to clone mouse Spacrcan; to characterize the promoter elements; to define the deduced amino acid sequence; to establish the time of Spacrcan expression during retinal development; and to determine the time of appearance and distribution of SPACRCAN protein. Spacrcan cDNA clone was obtained through PCR amplification of a mouse retina cDNA library, and RT-PCR amplification and 5'RACE of mouse retina RNA. The deduced polypeptide sequence of mouse SPACRCAN contains a signal peptide at the N-terminal, seven N-link glycosylation sites, numerous potential O-linked glycosylation sites in a central mucin-like domain, two glycosaminoglycan attachment sites, five potential hyaluronan-binding motifs, two epidermal growth factor-like domains, and a hydrophobic stretch of 23 amino acids near the C-terminal. Comparison of the genomic structure of mouse and human SPACRCAN showed significant structure conservation. Analysis of the promoter region revealed several important putative regulatory elements including a Ret-1/PCE-1 element, an 11 base motif for Crx binding, six copies of PIRE, a Ret-4 element, three copies of AP-1, a CRE element, and five copies of GATA3. Northern blot analysis and immunohistochemistry were used to determine the tissue specificity of Spacrcan mRNA and to localize SPACRCAN in developing retina. Spacrcan mRNA is expressed in both retina and pineal gland and was detectable as early as embryonic day 15. The protein is first detectable in the IPM at postnatal day 8 where it increases in concert with the extension of photoreceptor inner and outer segments from the outer retinal surface. The presence of several unique regulatory elements in the promoter region and characteristic molecular features shared with the orthologue in human and rat suggest an important functional role of SPACRCAN in the IPM. The time of appearance of the SPACRCAN protein during retinal development suggests that this matrix protein may establish the extracellular microenvironment into which photoreceptor outer segments are elaborated.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0014-4835
pubmed:author
pubmed:issnType
Print
pubmed:volume
76
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1-14
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12589770-Amino Acid Sequence, pubmed-meshheading:12589770-Animals, pubmed-meshheading:12589770-Base Sequence, pubmed-meshheading:12589770-Cloning, Molecular, pubmed-meshheading:12589770-DNA, Complementary, pubmed-meshheading:12589770-Gene Expression Regulation, Developmental, pubmed-meshheading:12589770-Genes, Regulator, pubmed-meshheading:12589770-Genome, pubmed-meshheading:12589770-Humans, pubmed-meshheading:12589770-Mice, pubmed-meshheading:12589770-Mice, Inbred BALB C, pubmed-meshheading:12589770-Mice, Inbred CBA, pubmed-meshheading:12589770-Molecular Sequence Data, pubmed-meshheading:12589770-Photoreceptor Cells, Vertebrate, pubmed-meshheading:12589770-Promoter Regions, Genetic, pubmed-meshheading:12589770-Proteoglycans, pubmed-meshheading:12589770-RNA, Messenger, pubmed-meshheading:12589770-Rats, pubmed-meshheading:12589770-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12589770-Species Specificity
pubmed:year
2003
pubmed:articleTitle
SPACRCAN in the interphotoreceptor matrix of the mouse retina: molecular, developmental and promoter analysis.
pubmed:affiliation
Cole Eye Institute (i31), The Cleveland Clinic Foundation, Cleveland, OH 44195, USA. chenq2@ccf.org
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't