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AssigneesInserm (Institut National De La Sante Et De La Recherche Medicale), Fondation Asile Des Aveugles, Universite De Paris, Assistance Publique-Hopitaux de Paris, Fondation Imagine
InventorsJean-Michel Rozet, Xavier Gerard, Iris Barny, Isabelle Perrault, Josseline Kaplan
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The invention relates to the skipping of the CEP290 exon 36 in an individual suffering from a retinal dystrophy accounted for by a nonsense mutation or a premature termination codon generated by a frameshift mutation in exon 36 or an upstream exon, including the c.4723A>T, c.4771C>T, c.4714G>T, c.4786_4790del, c.4791_4794del, c.4732G>T, c.4625_4626insCATG (35), c.4792_4795del, c.4801C>T, c.4805C>T, or c.4811G>A mutations, to bypass protein truncation and lessen retinal damages. Here, studying fibroblasts from control individuals, and two patients carrying the CEP290 c.4723A>T nonsense mutation, they show low levels of spontaneous skipping of exon 36 arising from both endogenous basal skipping and mutation-induced skipping. The minimally shortened and mutation-free CEP290 mRNA produced by skipping of exon 36 in the fibroblasts of the two patients is translated into a protein isoform that localizes at the centrosome and allows the formation of primary cilia, yet with elongated axonemes. Using an AON consisting of a sequence set forth as SEQ ID NO: 1, complementary to a nucleic acid sequence of CEP290 pre-mRNA, wherein said AON targeting an mRNA encoding the donor splice site (H36D) is capable to alter splicing by blocking the recognition of exon 36 and bypass protein truncation while maintaining the open reading frame, leading to the production of near full-length CEP290 protein, they were able to increase the abundance of the alternatively spliced mRNA and shortened protein and to reduce axonemal length in patient cells.
An antisense oligonucleotide consisting of a sequence set forth as SEQ ID NO:
A method for performing antisense oligonucleotide-mediated exon skipping in a subject in need thereof comprising delivering to target cells of the subject an amount of an antisense oligonucleotide, wherein the subject suffers from a retinal dystrophy caused by a mutation which modifies the splicing and/or creates a premature termination by a nonsense mutation in exon 36 of the CEP290 gene, or a frameshift mutation in exon 36 of the CEP290 gene, wherein said antisense oligonucleotide is complementary to a nucleic acid sequence of the CEP290 gene selected from the group consisting of the ESE sequences of said exon 36 and a sequence comprising the donor splice site around the exon 36/intron 36 boundary, and the antisense oligonucleotide performs antisense oligonucleotide-mediated exon skipping in the pre-mRNA from the CEP290 gene which mutation causes the retinal dystrophies in the target cells of the subject.
A method for restoring the function of CEP290 in a cell carrying a nonsense mutation in exon 36 of the CEP290 gene, or a frameshift mutation in exon 36, in a subject harbouring said mutation, comprising delivering to the subject an antisense oligonucleotide consisting of a sequence complementary to a nucleic acid sequence of the CEP290 gene that is necessary to alter splicing and excludes the exon encoding the premature termination codon inserted into CEP290 mRNA by a nonsense mutation in exon 36 or a frameshift mutation in exon 36 or an upstream exon, wherein the nucleic acid sequence of the CEP290 gene is selected from the group consisting of the exon splicing enhancer (ESE) sequences of said mutant exon 36 and a sequence comprising the donor splice site of CEP290 exon 36.
A method of treating a retinal dystrophy in a subject harbouring a nonsense mutation, located in exon 36 of the CEP290 gene or a frameshift mutation in exon 36 of the CEP290 gene or an upstream exon resulting in the apparition of a premature termination codon in exon 36, leading to a truncated protein, wherein said method comprises the step of modulating the splicing of the exon 36 which contains a nonsense mutation or a premature termination codon generated by a frameshift mutation within the same exon wherein said method is carried out by exposing CEP290 pre-mRNA to an antisense oligonucleotide (AONs) which is complementary to the exon splicing enhancer (ESE) sequences of said mutant exon 36 and a sequence comprising the donor splice site of CEP290 exon 36.
A method of treating a retinal dystrophy comprising delivering a pharmaceutical composition containing antisense oligonucleotide alone or in association with a vector, to a subject harbouring a nonsense mutation or a premature termination codon in exon 36 generated by a frameshift mutation within the same or an upstream exon mutation in the CEP290 gene, wherein the antisense oligonucleotide consists of a sequence complementary to a nucleic acid sequence of CEP290 gene that is necessary to alter splicing and exclude the exon encoding the premature termination codon inserted into the CEP290 mRNA by a nonsense mutation in exon 36 or a frameshift mutation in exon 36 or an upstream exon, and wherein said nucleic acid sequence of CEP290 gene is selected from the group consisting of the exon splicing enhancer (ESE) sequences of said mutant exon 36 and a sequence comprising the donor splice site of CEP290 exon 36.
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