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      A Critical Analysis of Atoh7 (Math5) mRNA Splicing in the Developing Mouse Retina

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      PLoS ONE
      Public Library of Science

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          Abstract

          The Math5 ( Atoh7) gene is transiently expressed during retinogenesis by progenitors exiting mitosis, and is essential for ganglion cell (RGC) development. Math5 contains a single exon, and its 1.7 kb mRNA encodes a 149-aa polypeptide. Mouse Math5 mutants have essentially no RGCs or optic nerves. Given the importance of this gene in retinal development, we thoroughly investigated the possibility of Math5 mRNA splicing by Northern blot, 3′RACE, RNase protection assays, and RT-PCR, using RNAs extracted from embryonic eyes and adult cerebellum, or transcribed in vitro from cDNA clones. Because Math5 mRNA contains an elevated G+C content, we used graded concentrations of betaine, an isostabilizing agent that disrupts secondary structure. Although ∼10% of cerebellar Math5 RNAs are spliced, truncating the polypeptide, our results show few, if any, spliced Math5 transcripts exist in the developing retina (<1%). Rare deleted cDNAs do arise via RT-mediated RNA template switching in vitro, and are selectively amplified during PCR. These data differ starkly from a recent study (Kanadia and Cepko 2010), which concluded that the vast majority of Math5 and other bHLH transcripts are spliced to generate noncoding RNAs. Our findings clarify the architecture of the Math5 gene and its mechanism of action. These results have implications for all members of the bHLH gene family, for any gene that is alternatively spliced, and for the interpretation of all RT-PCR experiments.

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          Most cited references69

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          Splicing regulation: from a parts list of regulatory elements to an integrated splicing code.

          Alternative splicing of pre-mRNAs is a major contributor to both proteomic diversity and control of gene expression levels. Splicing is tightly regulated in different tissues and developmental stages, and its disruption can lead to a wide range of human diseases. An important long-term goal in the splicing field is to determine a set of rules or "code" for splicing that will enable prediction of the splicing pattern of any primary transcript from its sequence. Outside of the core splice site motifs, the bulk of the information required for splicing is thought to be contained in exonic and intronic cis-regulatory elements that function by recruitment of sequence-specific RNA-binding protein factors that either activate or repress the use of adjacent splice sites. Here, we summarize the current state of knowledge of splicing cis-regulatory elements and their context-dependent effects on splicing, emphasizing recent global/genome-wide studies and open questions.
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            Exon recognition in vertebrate splicing.

            S Berget (1995)
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              Vertebrate neural cell-fate determination: lessons from the retina.

              Postmitotic neurons are produced from a pool of cycling progenitors in an orderly fashion during development. Studies of cell-fate determination in the vertebrate retina have uncovered several fundamental principles by which this is achieved. Most notably, a model for vertebrate cell-fate determination has been proposed that combines findings on the relative roles of extrinsic and intrinsic regulators in controlling cell-fate choices. At the heart of the model is the proposal that progenitors pass through intrinsically determined competence states, during which they are capable of giving rise to a limited subset of cell types under the influence of extrinsic signals.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2010
                24 August 2010
                14 September 2010
                : 5
                : 8
                : e12315
                Affiliations
                [1 ]Departments of Human Genetics and Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America
                [2 ]Division of Developmental Biology, Department of Pediatrics and Ophthalmology, Cincinnati Children's Research Foundation, University of Cincinnati School of Medicine, Cincinnati, Ohio, United States of America
                Stanford University, United States of America
                Author notes

                Conceived and designed the experiments: LP NLB TG. Performed the experiments: LP NLB. Analyzed the data: LP NLB TG. Wrote the paper: LP NLB TG.

                Article
                10-PONE-RA-20081
                10.1371/journal.pone.0012315
                2927423
                20808762
                adcb5a66-b7d2-4463-b831-321f314121f2
                Prasov et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 22 June 2010
                : 25 June 2010
                Page count
                Pages: 13
                Categories
                Research Article
                Developmental Biology/Molecular Development
                Developmental Biology/Neurodevelopment
                Developmental Biology/Organogenesis
                Genetics and Genomics/Gene Expression
                Molecular Biology/RNA Splicing
                Neuroscience/Neurodevelopment
                Developmental Biology/Molecular Development
                Developmental Biology/Neurodevelopment
                Developmental Biology/Organogenesis
                Genetics and Genomics/Gene Expression
                Molecular Biology/RNA Splicing
                Neuroscience/Neurodevelopment

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