Human Molecular Genetics Advance Access published online on September 20, 2008
Human Molecular Genetics, doi:10.1093/hmg/ddn305
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HnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
1 Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan 2 Department of Neurology and Neuromuscular Research Laboratory, Mayo Clinic, Rochester, Minnesota
To whom correspondence should be addressed at: Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya 466-8550, Japan, Phone: +81-52-744-2446, Fax: +81-52-744-2449, e-mail: ohnok{at}med.nagoya-u.ac.jp
Received May 19, 2008; Revised September 1, 2008; Accepted September 17, 2008
In humans and great apes, CHRNA1 encoding the muscle nicotinic acetylcholine receptor 
subunit carries an inframe exon P3A, the inclusion of which yields a nonfunctional subunit. In muscle, the P3A(-) and P3A(+) transcripts are generated in a 1:1 ratio but the functional significance and regulation of the alternative splicing remain elusive. An intronic mutation (IVS3-8G>A), identified in a patient with congenital myasthenic syndrome, disrupts an intronic splicing silencer (ISS) and results in exclusive inclusion of the downstream P3A exon. We found that the ISS-binding splicing trans-factor was hnRNP H and the mutation attenuated the affinity of hnRNP for the ISS 
100 fold. We next showed that direct placement of hnRNP H to the 3’ end of intron 3 silences, and siRNA-mediated downregulation of hnRNP H enhances recognition of exon P3A. Analysis of the human genome suggested that the hnRNP H-binding UGGG motif is overrepresented close to the 3’ ends of introns. Pursuing this clue, we showed that alternative exons of GRIP1, FAS, VPS13C, and NRCAM are downregulated by hnRNP H. Our findings imply that presence of the hnRNP H-binding motif close to the 3’ end of an intron is an essential but underestimated splicing regulator of the downstream exon.
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