ΔExon4 locus encodes mouse ZBP-89

Copyright information:Taken from "An isoform of ZBP-89 predisposes the colon to colitis"Nucleic Acids Research 2006;34(5):1342-1350.Published online 3 Mar 2006PMCID:PMC1390687.© The Author 2006. Published by Oxford University Press. All rights reserved () RT–PCR analysis was used to determ...

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Hauptverfasser: Law, David J., Labut, Edwin M., Adams, Rachael D., Merchant, Juanita L.
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Sprache:eng
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Zusammenfassung:Copyright information:Taken from "An isoform of ZBP-89 predisposes the colon to colitis"Nucleic Acids Research 2006;34(5):1342-1350.Published online 3 Mar 2006PMCID:PMC1390687.© The Author 2006. Published by Oxford University Press. All rights reserved () RT–PCR analysis was used to determine the variant mRNA structure in recombinant mice. Spleen whole-cell RNA was reverse-transcribed and amplified with primers within the indicated exons. RT–PCR of another ubiquitously expressed zinc-finger transcription factor, Sp1, was used for comparison and showed that the RNA samples were of uniform quality. Control experiments showed that PCR products were RT-dependent (data not shown), indicating that they were indeed derived from mRNA rather than possibly resulting from amplification of ZBP-89 related processed pseudogene sequences, such as ΨBERF1 (). () DNA sequencing of recombinant cDNA showed that deletion of exon 4 resulted in direct splicing of exon 3 to exon 5, excluding the Neo cassette. The resulting reading frameshift predicts an alternative initiation codon corresponding to M128 of FL protein, similar to the naturally occurring human ZBP-89 variant. () 2D immunoblot analysis of whole-cell spleen protein extracts from FL/FL, FL/ΔN and ΔN/ΔN mice, using conditions identical to those used for analysis of human samples ().
DOI:10.6084/m9.figshare.14866