beta-Spectrin Campinas: A novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosis

dc.creatorBasseres, DS
dc.creatorPranke, PHL
dc.creatorSales, TSI
dc.creatorCosta, FF
dc.creatorSaad, STO
dc.date1997
dc.dateJUN
dc.date2014-12-16T11:36:53Z
dc.date2015-11-26T16:25:45Z
dc.date2014-12-16T11:36:53Z
dc.date2015-11-26T16:25:45Z
dc.date.accessioned2018-03-28T23:06:29Z
dc.date.available2018-03-28T23:06:29Z
dc.identifierBritish Journal Of Haematology. Blackwell Science Ltd, v. 97, n. 3, n. 579, n. 585, 1997.
dc.identifier0007-1048
dc.identifierWOS:A1997XC93400013
dc.identifier10.1046/j.1365-2141.1997.932906.x
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/55436
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/55436
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/55436
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1268699
dc.descriptionbeta-Spectrin Campinas is a novel spectrin variant associated with a shortened beta-chain in a kindred with hereditary elliptocytosis (HE). The propositus and her mother exhibited increased amounts of spectrin dimers and an increase in the alpha I 74 kD fragment from the alpha-chain after partial tryptic digestion of spectrin. The shortened beta-chain appeared as an additional band of approximately 200kD on SDS-PAGE. In order to delineate the molecular defect of this abnormality at the gene level, reticulocyte mRNA was transcribed into cDNA and the last four exons of the beta-spectrin gene were amplified. Agarose gel of the amplification product of the propositus revealed the expected band of 487 bp as well as a shortened band of approximately 300 bp (size determined on gel). This shortened cDNA amplification product was cloned and nucleotide sequencing revealed the absence of the entire exon 30. In order to determine the underlying mutation responsible for this abnormal splicing, a genomic DNA fragment containing exons 30 and 31 was amplified and nucleotide sequencing revealed a G --> A substitution at the 5' donor splice site consensus sequence of intron 30 (nt+1 IVS30). The skip splicing observed in this study results in a frameshift, creating a new stop codon and causing a deletion of 129 aminoacids at the very COOH-terminus of the protein, thus impairing spectrin dimers self-association. We classified this HE as spherocytic HE because the propositus presented a few spherocytes in addition to many elliptocytes in the blood smear, whereas her mother, who was splenectomized, showed many schizocytes, poikilocytes and spherocytes.
dc.description97
dc.description3
dc.description579
dc.description585
dc.languageen
dc.publisherBlackwell Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationBritish Journal Of Haematology
dc.relationBr. J. Haematol.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectred cell membrane
dc.subjecthereditary elliptocytosis
dc.subjecttruncated beta-spectrin
dc.subjectsplicing
dc.subjectexon skipping
dc.subjectDeletional Frameshift Mutation
dc.subjectSplice Site Mutation
dc.subjectClinical Expression
dc.subjectErythrocyte-membrane
dc.subjectNice Beta-220/216
dc.subjectMolecular Defect
dc.subjectSelf-association
dc.subjectGene
dc.subjectProteins
dc.subjectPyropoikilocytosis
dc.titlebeta-Spectrin Campinas: A novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosis
dc.typeArtículos de revistas


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