On 3 mutations in MM patients may contribute to aberrant splicing of HAS1 in malignant cells from patients, where HAS1Vb is more frequent than HAS1Vd.DiscussionIn this work we show that mutations and deletions in introns 3 and 4 of HAS1 can alter pre-mRNA splicing events to promote aberrant splicing of the type detected in malignant cells from patients with MM. Among splice variants, although HAS1Va (exon 4 skipped) is common, HAS1Vb (exon 4 skipped and 59 bp downstream intron 4 retained) appears to be clinically more relevant because in MM, its overexpression correlates with the worst clinical outcome. Since aberrant splicing involves exons 3-45, it seems likely that frequent mutations in introns 3 and 4 may be involved in the selection of splice sites for pre-mRNA splicing. We utilized HAS1 minigene transfection to evaluate splicing profiles. A newly identified intronic splice variant, HAS1Vd, utilizes an otherwise cryptic splice site in intron 4 to generate a transcript including a segment of intron 4 and encoding a truncated protein. For constructs with unaltered introns 3 and 4, KS-176 HAS1Vd transcripts are readily detectable, frequently to the exclusion of HAS1Vb which utilizes the same intron 4 splice site. In contrast, HAS1Vb isTable 2. Splicing enhancers (ISE) and silencers (ESS) in the Grich region of HAS1 intron 3.Locations1 G7, G15, G16, G20, G28 G8?, G11?2, G26, G27?8 G26, GSequence GGGGCTG GGGGTTGGGA GGGATGGGGTType of element References ISE (SF1) ESS ESS [28,34] [35,36] [35]Location of each G-motif is shown in Figure 3. doi:10.1371/journal.pone.0053469.tIntronic Changes Alter HAS1 SplicingFigure 5. Mutagenesis of G-repeat motifs in del1 promotes HAS1Vb expression. Selected G-repeat motifs in del1 (striped line) were mutagenized according to sequences shown in Figure 3. Splicing profiles driven by various del1 derivatives were analyzed by RT-PCR using E3/E5 primer set and products were analyzed by agarose gel electrophoresis. doi:10.1371/journal.pone.0053469.gFigure 4. Mutagenesis of G-repeat motifs in HAS1 intron 3 enhances exon 4 skipping. Selected G-repeat motifs in G345 (striped line) were mutagenized according to sequences shown in Figure 3. Splicing profiles driven by various G345 derivatives were analyzed by RT-PCR using E3/E5 primer set and agarose gel electrophoresis (A). Product in box is not FL as determined by DNA fragment analysis (data not shown). Abnormal HAS1 transcripts driven by G345/G1?8 are summarized in (B). PCR products of G345/G1?8 m transfectants were cloned and spliced junctions were identified by sequencing of subclones. Arrows indicate authentic and cryptic donor sites which located 144 and 279 bp downstream of authentic donor site. The strength of each donor site is determined according to splice site prediction by a neural network (http://www.fruitfly.org/seq_tools/ splice.html). doi:10.1371/journal.pone.0053469.gdetected more frequently in patient cells where HAS1Vd is infrequent. For nearly half of MM patients, HAS1Vb is expressed in the MM clone at the time of diagnosis [19,21]. For patients lacking HAS1 splice variants at diagnosis, these transcripts were often detected at later stages of disease [19]. Analysis of a series of directed deletions in HAS1 intron 4 showed that splicing of HAS1Vd could be elevated, but HAS1Vb remained unaffected, despite their use of the same 39 splice site in intron 4. Thus, changes in intron 4 alone were insufficient to promote the splicing pattern observed in 115103-85-0 patien.On 3 mutations in MM patients may contribute to aberrant splicing of HAS1 in malignant cells from patients, where HAS1Vb is more frequent than HAS1Vd.DiscussionIn this work we show that mutations and deletions in introns 3 and 4 of HAS1 can alter pre-mRNA splicing events to promote aberrant splicing of the type detected in malignant cells from patients with MM. Among splice variants, although HAS1Va (exon 4 skipped) is common, HAS1Vb (exon 4 skipped and 59 bp downstream intron 4 retained) appears to be clinically more relevant because in MM, its overexpression correlates with the worst clinical outcome. Since aberrant splicing involves exons 3-45, it seems likely that frequent mutations in introns 3 and 4 may be involved in the selection of splice sites for pre-mRNA splicing. We utilized HAS1 minigene transfection to evaluate splicing profiles. A newly identified intronic splice variant, HAS1Vd, utilizes an otherwise cryptic splice site in intron 4 to generate a transcript including a segment of intron 4 and encoding a truncated protein. For constructs with unaltered introns 3 and 4, HAS1Vd transcripts are readily detectable, frequently to the exclusion of HAS1Vb which utilizes the same intron 4 splice site. In contrast, HAS1Vb isTable 2. Splicing enhancers (ISE) and silencers (ESS) in the Grich region of HAS1 intron 3.Locations1 G7, G15, G16, G20, G28 G8?, G11?2, G26, G27?8 G26, GSequence GGGGCTG GGGGTTGGGA GGGATGGGGTType of element References ISE (SF1) ESS ESS [28,34] [35,36] [35]Location of each G-motif is shown in Figure 3. doi:10.1371/journal.pone.0053469.tIntronic Changes Alter HAS1 SplicingFigure 5. Mutagenesis of G-repeat motifs in del1 promotes HAS1Vb expression. Selected G-repeat motifs in del1 (striped line) were mutagenized according to sequences shown in Figure 3. Splicing profiles driven by various del1 derivatives were analyzed by RT-PCR using E3/E5 primer set and products were analyzed by agarose gel electrophoresis. doi:10.1371/journal.pone.0053469.gFigure 4. Mutagenesis of G-repeat motifs in HAS1 intron 3 enhances exon 4 skipping. Selected G-repeat motifs in G345 (striped line) were mutagenized according to sequences shown in Figure 3. Splicing profiles driven by various G345 derivatives were analyzed by RT-PCR using E3/E5 primer set and agarose gel electrophoresis (A). Product in box is not FL as determined by DNA fragment analysis (data not shown). Abnormal HAS1 transcripts driven by G345/G1?8 are summarized in (B). PCR products of G345/G1?8 m transfectants were cloned and spliced junctions were identified by sequencing of subclones. Arrows indicate authentic and cryptic donor sites which located 144 and 279 bp downstream of authentic donor site. The strength of each donor site is determined according to splice site prediction by a neural network (http://www.fruitfly.org/seq_tools/ splice.html). doi:10.1371/journal.pone.0053469.gdetected more frequently in patient cells where HAS1Vd is infrequent. For nearly half of MM patients, HAS1Vb is expressed in the MM clone at the time of diagnosis [19,21]. For patients lacking HAS1 splice variants at diagnosis, these transcripts were often detected at later stages of disease [19]. Analysis of a series of directed deletions in HAS1 intron 4 showed that splicing of HAS1Vd could be elevated, but HAS1Vb remained unaffected, despite their use of the same 39 splice site in intron 4. Thus, changes in intron 4 alone were insufficient to promote the splicing pattern observed in patien.
