GgaEX1014125 @ galGal4
Exon Skipping
Gene
ENSGALG00000000608 | CDH1
Description
cadherin-1 precursor [Source:RefSeq peptide;Acc:NP_001034347]
Coordinates
chr11:18323342-18324110:+
Coord C1 exon
chr11:18323342-18323586
Coord A exon
chr11:18323663-18323805
Coord C2 exon
chr11:18323886-18324110
Length
143 bp
Sequences
Splice sites
3' ss Seq
TGACTGCTCCCTCCGCCCAGGTA
3' ss Score
8.95
5' ss Seq
ATGGTGAGG
5' ss Score
7.61
Exon sequences
Seq C1 exon
GGCCTGGATTATGAGACCAAGAGCCGCTACGACCTGGTGGTGACGGTGGAGAACAAAGTGCCCCTGTCCGTGCCCATCACACTCTCCACCGCCAGCGTCCTGGTGACCGTCCTGGACGTGAATGAGCCCCCTGTCTTCGTGCCCCCTATCAAGAGGGTAGGGGTACCAGAGGACCTACCAGTGGGGCAGCAGGTTACATCCTACACGGCCCAAGACCCCGACAGGGACATGAGGCAGAAGATCAC
Seq A exon
GTACCGCATGGGCAGCGACCCAGCAGGCTGGCTGTACATTCACCCCGAGAATGGCATTGTCACGGCCACCCAGCCACTGGACCGCGAGTCGGTGCACGCCATCAACAGTACATACAAGGCCATCATCCTGGCTGTGGACAATG
Seq C2 exon
GGATACCGGATACCACCGGTACGGGGACGCTGCTGCTGCTCCTCCAGGATGTGAATGACAACGGGCCCACCCCAGAGCCCCGGTCCTTCGAGATCTGCAGCCGGCAGCCTGAGAAGCAGATACTGAGCATTGTGGACAAGGACCTGCCCCCACATACCTACCCCTTCAAGGCAGCACTGGAGCATGGTTCCAGCAACAACTGGACTGTTGAGATAAGGGGCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000608-'15-15,'15-13,16-15
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.256 A=0.122 C2=0.237
Domain overlap (PFAM):
C1:
PF0002812=Cadherin=PD(37.0=45.1),PF0002812=Cadherin=PU(32.6=37.8)
A:
PF0002812=Cadherin=FE(50.5=100)
C2:
PF0002812=Cadherin=PD(15.8=19.7),PF0002812=Cadherin=PU(55.2=63.2)

Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GCAGGTTACATCCTACACGGC
R:
AGTTGTTGCTGGAACCATGCT
Band lengths:
258-401
Functional annotations
There are 2 annotated functions for this event
PMID: 19745069
The study used a microarray technique to screen for genes that up-regulate their RNA signal upon nonsense-mediated decay pathway blockade in chronic lymphocytic leukemia (CLL) specimens and identified an E-cadherin transcript with premature termination codon (PTC). Sequencing revealed an aberrant E-cadherin transcript lacking exon 11 (HsaEX0014149), resulting in a frameshift and PTC. The aberrant E-cadherin transcript was also identified in normal B cells, but occurred at a much lower level compared with CLL cells. In CLL specimens, E-cadherin expression was depressed more than 50% in 62% cases (relative to normal B cells). By real-time polymerase chain reaction analysis, the relative amounts of wild-type transcript inversely correlated with amounts of aberrant transcript (P = .018). Ectopic expression of E-cadherin in CLL specimens containing high amounts of aberrant transcript resulted in down-regulation of the wnt?beta-catenin pathway reporter, a pathway known to be up-regulated in CLL. These data point to a novel mechanism of E-cadherin gene inactivation, with CLL cells displaying a higher proportion of aberrant nonfunctional transcripts and resulting up-regulation of the wnt?beta-catenin pathway.
PMID: 21764905
[Disease and regulation]. The study analyzed the role of E-cadherin missplicing as a mechanism of its downregulation by analyzing a misspliced E-cadherin transcript that lacks exon 11 (HsaEX0014149) of this gene. This results in a frameshift and a premature termination codon that targets this transcript for degradation. Tumor tissues, including breast (20%, n = 9), prostate (30%, n = 9) and head and neck (75%, n = 8) cancer, express the exon 11-skipped transcripts (vs. nonmalignant controls) and its levels inversely correlate with E-cadherin expression. This is a novel mechanism of E-cadherin downregulation by missplicing in tumor cells, which is observed in highly prevalent human tumors. In the head and neck cancer model, nontumorigenic keratinocytes express exon 11-skipped splice product two- to sixfold lower than the head and neck tumor cell lines. Mechanistic studies reveal that SFRS2 (SC35), a splicing factor, as one of the regulators that increases missplicing and downregulates E-cadherin expression. Furthermore, this splicing factor was found to be overexpressed in 5 of 7 head and neck cell lines and primary head and neck tumors. Also, methylation of E-cadherin gene acts as a regulator of this aberrant splicing process. In 2 head and neck cell lines, wild-type transcript expression increased 16- to 25-folds, whereas the percentage of exon 11-skipped transcripts in both the cell lines decreased five- to 30-folds when cells were treated with a hypomethylating agent, azacytidine. These findings reveal that promoter methylation and an upregulated splicing factor (SFRS2) are involved in the E-cadherin missplicing in tumors.
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]