US20190119679A1

US20190119679A1 - METHODS AND MEANS FOR EFFICIENT SKIPPING OF EXON 45 IN DUCHENNE MUSCULAR DYSTROPHY PRE-mRNA

Info

Publication number: US20190119679A1
Application number: US16/229,821
Authority: US
Inventors: Josephus Johannes De Kimpe; Adriana Marie Rus; Gerard Johannes Platenburg; Judith Christina Theodora Van Deutekom; Garrit-Jan Boudewijn van Ommen
Original assignee: Leids Universitair Medisch Centrum LUMC; Biomarin Technologies BV
Current assignee: Leids Universitair Medisch Centrum LUMC; Biomarin Technologies BV
Priority date: 2007-10-26
Filing date: 2018-12-21
Publication date: 2019-04-25
Also published as: JP2017141296A; ES2692886T3; CN102256606A; US20210139904A1; JP5600064B2; EP2614827A2; EP2614827A3; JP2016033140A; CN102264903B; IL284321B; JP2021113229A; JP7107622B2; US20230151362A1; ES2914775T3; PT2203173E; EP3238737A1; US20200239886A1; JP6885620B2; ES2639852T3; JP6579629B2

Abstract

The. invention relates to a method for inducing or promoting skipping of exon 45 of DMD pre-mRNA in a Duchenne Muscular Dystrophy patient, preferably in an isolated (muscle) cell, the method comprising providing said cell with an antisense molecule that binds to a continuous stretch of at least 21 nucleotides within said exon. The invention further relates to such antisense molecule used in said method.

Description

FIELD

The invention relates to the field of genetics, more specifically human genetics. The invention in particular relates to the modulation of splicing of the human Duchenne Muscular Dystrophy pre-mRNA.

BACKGROUND OF THE INVENTION

Myopathies are disorders that result in functional impairment of muscles. Muscular dystrophy (MD) refers to genetic diseases that are characterized by progressive weakness and degeneration of skeletal muscles. Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are the most common childhood forms of muscular dystrophy. They are recessive disorders and because the gene responsible for DMD and BMD resides on the X-chromosome, mutations mainly affect males with an incidence of about 1 in 3500 boys.
DMD and BMD are caused by genetic defects in the DMD gene encoding dystrophin, a muscle protein that is required for interactions between the cytoskeleton and the extracellular matrix to maintain muscle fiber stability during contraction. DMD is a severe, lethal neuromuscular disorder resulting in a dependency on wheelchair support before the age of 12 and DMD patients often die before the age of thirty due to respiratory- or heart failure. In contrast, BMD patients often remain ambulatory until later in life, and have near normal life expectancies. DMD mutations in the DMD gene are mainly characterized by frame shifting insertions or deletions or nonsense point mutations, resulting in the absence of functional dystrophin. BMD mutations in general keep the reading frame intact, allowing synthesis of a partly functional dystrophin. During the last decade, specific modification of splicing in order to restore the disrupted reading frame of the DMD transcript has emerged as a promising therapy for Duchenne muscular dystrophy (DMD) (van Ommen, van Deutekom, Aartsma-Rus, Curr Opin Mol Ther. 2008;10(2)140-9, Yokota, Duddy, Partidge, Acta Myol. 2007;26(3)179-84, van Deutekom et al., N Engl J Med. 2007;357(26)2677-86).
Using antisense oligonucleotides (AONs) interfering with splicing signals the skipping of specific exons can be induced in the DMD pre-mRNA, thus restoring the open reading frame and converting the severe DMD into a milder BMD phenotype (van Deutekom et al. Hum Mol Genet. 2001; 10: 1547-54; Aartsma-Rus et al., Hum Mol Genet 2003; 12(8)907-14.). In vivo proof-of-concept was first obtained in the mdx mouse model, which is dystrophin-deficient due to a nonsense mutation in exon 23. Intramuscular and intravenous injections of AONs targeting the mutated exon 23 restored dystrophin expression for at least three months (Lu et al. Nat Med. 2003; 8: 1009-14; Lu et al., Proc Natl Acad Sci U S A. 2005;102(1)198-203). This was accompanied by restoration of dystrophin-associated proteins at the fiber membrane as well as functional improvement of the treated muscle. In vivo skipping of human exons has also been achieved in the hDMD mouse model, which contains a complete copy of the human DMD gene integrated in chromosome 5 of the mouse (Bremmer-Bout et al. Molecular Therapy. 2004; 10: 232-40; 't Hoen et al. J Biol Chem. 2008; 283: 5899-907).
As the majority of DMD patients have deletions that cluster in hotspot regions, the skipping of a small number of exons is applicable to relatively large numbers of patients. The actual applicability of exon skipping can be determined for deletions, duplications and point mutations reported in DMD mutation databases such as the Leiden DMD mutation database available at www.dmd.nl. Therapeutic skipping of exon 45 of the DMD pre-mRNA would restore the open reading frame of DMD patients having deletions including but not limited to exons 12-44, 18-44, 44, 46, 46-47, 46-48, 46-49, 46-51, 46-53, 46-55, 46-59, 46-60 of the DMD pre-mRNA, occurring in a total of 16% of all DMD patients with a deletion (Aartsma-Rus and van Deutekom, 2007, Antisense Elements (Genetics) Research Focus, 2007 Nova Science Publishers, Inc). Furthermore, for some DMD patients the simultaneous skipping of one of more exons in addition to exon 45, such as exons 51 or 53 is required to restore the correct reading frame. None-limiting examples include patients with a deletion of exons 46-50 requiring the co-skipping of exons 45 and 51, or with a deletion of exons 46-52 requiring the co-skipping of exons 45 and 53.
Recently, a first-in-man study was successfully completed where an AON inducing the skipping of exon 51 was injected into a small area of the tibialis anterior muscle of four DMD patients. Novel dystrophin expression was observed in the majority of muscle fibers in all four patients treated, and the AON was safe and well tolerated (van Deutekom et al. N Engl J Med. 2007; 357: 2677-86).
Most AONs studied contain up to 20 nucleotides, and it has been argued that this relatively short size improves the tissue distribution and/or cell penetration of an AON. However, such short AONs will result in a limited specificity due to an increased risk for the presence of identical sequences elsewhere in the genome, and a limited target binding or target affinity due to a low free energy of the AON-target complex. Therefore the inventors decided to design new and optionally improved oligonucleotides that would not exhibit all of these drawbacks.

DESCRIPTION OF THE INVENTION

Method
In a first aspect, the invention provides a method for inducing and/or promoting skipping of exon 45 of DMD pre-mRNA in a patient, preferably in an isolated cell of said patient, the method comprising providing said cell and/or said patient with a molecule that binds to a continuous stretch of at least 21 nucleotides within said exon.
Accordingly, a method is herewith provided for inducing and/or promoting skipping of exon 45 of DMD pre-mRNA, preferably in an isolated cell of a patient, the method comprising providing said cell and/or said patient with a molecule that binds to a continuous stretch of at least 21 nucleotides within said exon.
It is to be understood that said method encompasses an in vitro, in vivo or ex vivo method.
As defined herein a DMD pre-mRNA preferably means the pre-mRNA of a DMD gene of a DMD or BMD patient. The DMD gene or protein corresponds to the dystrophin gene or protein.
A patient is preferably intended to mean a patient having DMD or BMD as later defined herein or a patient susceptible to develop DMD or BMD due to his or her genetic background.
Exon skipping refers to the induction in a cell of a mature mRNA that does not contain a particular exon that is normally present therein. Exon skipping is achieved by providing a cell expressing the pre-mRNA of said mRNA with a molecule capable of interfering with sequences such as, for example, the splice donor or splice acceptor sequence that are both required for allowing the enzymatic process of splicing, or a molecule that is capable of interfering with an exon inclusion signal required for recognition of a stretch of nucleotides as an exon to be included in the mRNA. The term pre-mRNA refers to a non-processed or partly processed precursor mRNA that is synthesized from a DNA template in the cell nucleus by transcription.
Within the context of the invention inducing anchor promoting skipping of an exon as indicated herein means that at least 1%, 10%, 20%, 30%, 40%,50%, 60%, 70%, 80%, 90% or more of the DMD mRNA in one or more (muscle) cells of a treated patient will not contain said exon. This is preferably assessed by PCR as described in the examples.
Preferably, a method of the invention by inducing or promoting skipping of exon 45 of the DMD pre-mRNA in one or more cells of a patient provides said patient with a functional dystrophin protein and/or decreases the production of an aberrant dystrophin protein in said patient. Therefore a preferred method is a method, wherein a patient or a cell of said patient is provided with a functional dystrophin protein and/or wherein the production of an aberrant dystrophin protein in said patient or in a cell of said patient is decreased
Decreasing the production of an aberrant dystrophin may be assessed at the mRNA level and preferably means that 99%, 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10%, 5% or less of the initial amount of aberrant dystrophin mRNA, is still detectable by RT PCR. An aberrant dystrophin mRNA or protein is also referred to herein as a non-functional dystrophin mRNA or protein. A non functional dystrophin protein is preferably a dystrophin protein which is not able to bind actin and/or members of the DGC protein complex. A non-functional dystrophin protein or dystrophin mRNA does typically not have, or does not encode a dystrophin protein with an intact C-terminus of the protein.
Increasing the production of a functional dystrophin in said patient or in a cell of said patient may be assessed at the mRNA level (by RT-PCR analysis) and preferably means that a detectable amount of a functional dystrophin mRNA is detectable by RT PCR. In another embodiment, 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the detectable dystrophin mRNA is a functional dystrophin mRNA. Increasing the production of a functional dystrophin in said patient or in a cell of said patient may be assessed at the protein level (by immuno fluorescence and western blot analyses) and preferably means that a detectable amount of a functional dystrophin protein is detectable by immunofluorescence or western blot analysis. In another embodiment, 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the detectable dystrophin protein is a functional dystrophin protein.
As defined herein, a functional dystrophin is preferably a wild type dystrophin corresponding to a protein having the amino acid sequence as identified in SEQ ID NO: 1. A functional dystrophin is preferably a dystrophin, which has an actin binding domain in its N terminal part (first 240 amino acids at the N terminus), a cystein-rich domain (amino acid 3361 till 3685) and a C terminal domain (last 325 amino acids at the C terminus) each of these domains being present in a wild type dystrophin as known to the skilled person. The amino acids indicated herein correspond to amino acids of the wild type dystrophin being represented by SEQ ID NO:l. In other words, a functional dystrophin is a dystrophin which exhibits at least to some extent an activity of a wild type dystrophin. “At least to some extent” preferably means at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% of a corresponding activity of a wild type functional dystrophin. In this context, an activity of a functional dystrophin is preferably binding to actin and to the dystrophin-associated glycoprotein complex (DGC) (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). Binding of dystrophin to actin and to the DGC complex may be visualized by either co-immunoprecipitation using total protein extracts or immunofluorescence analysis of cross-sections, from a muscle biopsy, as known to the skilled person.
Individuals or patients suffering from Duchenne muscular dystrophy typically have a mutation in the DMD gene that prevent synthesis of the complete dystrophin protein, i.e of a premature stop prevents the synthesis of the C-terminus. In Becker muscular dystrophy the DMD gene also comprises a mutation compared to the wild type gene but the mutation does typically not induce a premature stop and the C-terminus is typically synthesized. As a result a functional dystrophin protein is synthesized that has at least the same activity in kind as the wild type protein, not although not necessarily the same amount of activity. The genome of a BMD individual typically encodes a dystrophin protein comprising the N terminal part (first 240 amino acids at the N terminus), a cystein-rich domain (amino acid 3361 till 3685) and a C terminal domain (last 325 amino acids at the C terminus) but its central rod shaped domain may be shorter than the one of a wild type dystrophin (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). Exon—skipping for the treatment of DMD is typically directed to overcome a premature stop in the pre-mRNA by skipping an exon in the rod-shaped domain to correct the reading frame and allow synthesis of the remainder of the dystrophin protein including the C-terminus, albeit that the protein is somewhat smaller as a result of a smaller rod domain. In a preferred embodiment, an individual having DMD and being treated by a method as defined herein will be provided a dystrophin which exhibits at least to some extent an activity of a wild type dystrophin. More preferably, if said individual is a Duchenne patient or is suspected to be a Duchenne patient, a functional dystrophin is a dystrophin of an individual having BMD: typically said dystrophin is able to interact with both actin and the DGC, but its central rod shaped domain may be shorter than the one of a wild type dystrophin (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). The central rod-shaped domain of wild type dystrophin comprises 24 spectrin-like repeats (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). For example, a central rod-shaped domain of a dystrophin as provided herein may comprise 5 to 23, 10 to 22 or 12 to 18 spectrin-like repeats as long as it can bind to actin and to DGC.
A method of the invention may alleviate one or more characteristics of a muscle cell from a DMD patient comprising deletions including but not limited to exons 12-44, 18-44, 44, 46, 46-47, 46-48, 46-49, 46-51, 46-53, 46-55, 46^-59, 46^-60 of the DMD pre-mRNA of said patient (Aartsma-Rus and van Deutekom, 2007, Antisense Elements (Genetics) Research Focus, 2007 Nova Science Publishers, Inc) as well as from DMD patients requiring the simultaneous skipping of one of more exons in addition to exon 45 including but not limited to patients with a deletion of exons 46-50 requiring the co-skipping of exons 45 and 51, or with a deletion of exons 46-52 requiring the co-skipping of exons 45 and 53.
In a preferred method, one or more symptom(s) or characteristic(s) of a myogenic cell or muscle cell from a DMD patient is/are alleviated. Such symptoms or characteristics may be assessed at the cellular, tissue level or on the patient self.
An alleviation of one or more symptoms or characteristics may be assessed by any of the following assays on a myogenic cell or muscle cell from a patient: reduced calcium uptake by muscle cells, decreased collagen synthesis, altered morphology, altered lipid biosynthesis, decreased oxidative stress, and/or improved muscle fiber function, integrity, and/or survival. These parameters are usually assessed using immunofluorescence and/or histochemical analyses of cross sections of muscle biopsies.
The improvement of muscle fiber function, integrity and/or survival may also be assessed using at least one of the following assays: a detectable decrease of creatine kinase in blood, a detectable decrease of necrosis of muscle fibers in a biopsy cross-section of a muscle suspected to be dystrophic, and/or a detectable increase of the homogeneity of the diameter of muscle fibers in a biopsy cross-section of a muscle suspected to be dystrophic. Each of these assays is known to the skilled person.
Creatine kinase may be detected in blood as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). A detectable decrease in creatine kinase may mean a decrease of 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more compared to the concentration of creatine kinase in a same DMD patient before treatment.
A detectable decrease of necrosis of muscle fibers is preferably assessed in a muscle biopsy, more preferably as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006) using biopsy cross-sections. A detectable decrease of necrosis may be a decrease of 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the area wherein necrosis has been identified using biopsy cross-sections. The decrease is measured by comparison to the necrosis as assessed in a same DMD patient before treatment.
A detectable increase of the homogeneity of the diameter of muscle fibers is preferably assessed in a muscle biopsy cross-section, more preferably as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). The increase is measured by comparison to the homogeneity of the diameter of muscle fibers in a muscle biopsy cross-section of a same DMD patient before treatment.
An alleviation of one or more symptoms or characteristics may be assessed by any of the following assays on the patient self: prolongation of time to loss of walking, improvement of muscle strength, improvement of the ability to lift weight, improvement of the time taken to rise from the floor, improvement in the nine-meter walking time, improvement in the time taken for four-stairs climbing, improvement of the leg function grade, improvement of the pulmonary function, improvement of cardiac function, improvement of the quality of life. Each of these assays is known to the skilled person. As an example, the publication of Manzur at al (Manzur A Y et al, (2008), Glucocorticoid corticosteroids for Duchenne muscular dystrophy (review), Wiley publishers, The Cochrane collaboration.) gives an extensive explanation of each of these assays. For each of these assays, as soon as a detectable improvement or prolongation of a parameter measured in an assay has been found, it will preferably mean that one or more symptoms of Duchenne Muscular Dystrophy has been alleviated in an individual using a method of the invention. Detectable improvement or prolongation is preferably a statistically significant improvement or prolongation as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). Alternatively, the alleviation of one or more symptom(s) of Duchenne Muscular Dystrophy may be assessed by measuring an improvement of a muscle fiber function, integrity and/or survival as later defined herein.
A treatment in a method according to the invention may have a duration of at least one week, at least one month, at least several months, at least one year, at least 2, 3, 4, 5, 6 years or more. The frequency of administration of an oligonucleotide, composition, compound of the invention may depend on several parameters such as the age of the patient, the type of mutation, the number of molecules (dose), the formulation of said molecule. The frequency may be ranged between at least once in a two weeks, or three weeks or four weeks or five weeks or a longer time period. Each molecule or oligonucleotide or equivalent thereof as defined herein for use according to the invention may be suitable for direct administration to a cell, tissue and/or an organ in vivo of individuals affected by or at risk of developing DMD and may be administered directly in vivo, ex vivo or in vitro. An oligonucleotide as used herein may be suitable for administration to a cell, tissue and/or an organ in vivo of individuals affected by or at risk of developing DMD, and may be administered in vivo, ex vivo or in vitro. Said oligonucleotide may be directly or indirectly administrated to a cell, tissue and/or an organ in vivo of an individual affected by or at risk of developing DMD, and may be administered directly or indirectly in vivo, ex vivo or in vitro. As Duchenne muscular dystrophy has a pronounced phenotype in muscle cells, it is preferred that said cells are muscle cells, it is further preferred that said tissue is a muscular tissue and/or it is further preferred that said organ comprises or consists of a muscular tissue. A preferred organ is the heart. Preferably said cells comprise a gene encoding a mutant dystrophin protein. Preferably said cells are cells of an individual suffering from DMD.
A molecule or oligonucleotide or equivalent thereof can be delivered as is to a cell. When administering said molecule, oligonucleotide or equivalent thereof to an individual, it is preferred that it is dissolved in a solution that is compatible with the delivery method. For intravenous, subcutaneous, intramuscular, intrathecal and/or intraventricular administration it is preferred that the solution is a physiological salt solution. Particularly preferred for a method of the invention is the use of an excipient that will further enhance delivery of said molecule, oligonucleotide or functional equivalent thereof as defined herein, to a cell and into a cell, preferably a muscle cell. Preferred excipient are defined in the section entitled “pharmaceutical composition”. In vitro, we obtained very good results using polyethylenimine (PEI, ExGen500, MBI Fermentas) as shown in the example.
In a preferred method of the invention, an additional molecule is used which is able to induce and/or promote skipping of a distinct exon of the DMD pre-mRNA of a patient. Preferably, the second exon is selected from: exon 7, 44, 46, 51, 53, 59, 67 of the dystrophin pre-mRNA of a patient. Molecules which can be used are depicted in table 2. Preferred molecules comprise or consist of any of the oligonucleotides as disclosed in table 2. Several oligonucleotides may also be used in combination.This way, inclusion of two or more exons of a DMD pre-mRNA in mRNA produced from this pre-mRNA is prevented. This embodiment is further referred to as double- or multi-exon skipping (Aartsma-Rus A, Janson A A, Kaman W E, et al. Antisense-induced multiexon skipping for Duchenne muscular dystrophy makes more sense. Am J Hum Genet 2004;74(1):83-92, Aartsma-Rus A, Kaman W E, Weij R, den Dunnen J T, van Ommen G J, van Deutekom J C. Exploring the frontiers of therapeutic exon skipping for Duchenne muscular dystrophy by double targeting within one or multiple exons. Mol Ther 2006;14(3):401-7). In most cases double-exon skipping results in the exclusion of only the two targeted exons from the dystrophin pre-mRNA. However, in other cases it was found that the targeted exons and the entire region in between said exons in said pre-mRNA were not present in the produced mRNA even when other exons (intervening exons) were present in such region. This multi-skipping was notably so for the combination of oligonucleotides derived from the DMD gene, wherein one oligonucleotide for exon 45 and one oligonucleotide for exon 51 was added to a cell transcribing the DMD gene. Such a set-up resulted in mRNA being produced that did not contain exons 45 to 51. Apparently, the structure of the pre-mRNA in the presence of the mentioned oligonucleotides was such that the splicing machinery was stimulated to connect exons 44 and 52 to each other.
It is possible to specifically promote the skipping of also the intervening exons by providing a linkage between the two complementary oligonucleotides. Hence, in one embodiment stretches of nucleotides complementary to at least two dystrophin exons are separated by a linking moiety. The at least two stretches of nucleotides are thus linked in this embodiment so as to form a single molecule.
In case, more than one compounds are used in a method of the invention, said compounds can be administered to an individual in any order. In one embodiment, said compounds are administered simultaneously (meaning that said compounds are administered within 10 hours, preferably within one hour). This is however not necessary. In another embodiment, said compounds are administered sequentially.
Molecule
In a second aspect, there is provided a molecule for use in a method as described in the previous section entitled “Method”. This molecule preferably comprises or consists of an oligonucleotide, Said oligonucleotide is preferably an antisense oligonucleotide (AON) or antisense oligoribonucleotide.
It was found by the present investigators that especially exon 45 is specifically skipped at a high frequency using a molecule that binds to a continuous stretch of at least 21 nucleotides within said exon. Although this effect can be associated with a higher binding affinity of said molecule, compared to a molecule that binds to a continuous stretch of less than 21 nucleotides, there could be other intracellular parameters involved that favor thermodynamic, kinetic, or structural characteristics of the hybrid duplex. In a preferred embodiment, a molecule that binds to a continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides within said exon is used.
In a preferred embodiment, a molecule or an oligonucleotide of the invention which comprises a sequence that is complementary to a part of exon 45 of DMD pre-mRNA is such that the complementary part is at least 50% of the length of the oligonucleotide of the invention, more preferably at least 60%, even more preferably at least 70%, even more preferably at least 80%, even more preferably at least 90% or even more preferably at least 95%, or even more preferably 98% and most preferably up to 100%. “A part of exon 45” preferably means a stretch of at least 21 nucleotides. In a most preferred embodiment, an oligonucleotide of the invention consists of a sequence that is complementary to part of exon 45 dystrophin pre-mRNA as defined herein. Alternatively, an oligonucleotide may comprise a sequence that is complementary to part of exon 45 dystrophin pre-mRNA as defined herein and additional flanking sequences. In a more preferred embodiment, the length of said complementary part of said oligonucleotide is of at least 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50 nucleotides. Several types of flanking sequences may be used. Preferably, additional flanking sequences are used to modify the binding of a protein to said molecule or oligonucleotide, or to modify a thermodynamic property of the oligonucleotide, more preferably to modify target RNA binding affinity. In another preferred embodiment, additional flanking sequences are complementary to sequences of the DMD pre-mRNA which are not present in exon 45. Such flanking sequences are preferably complementary to sequences comprising or consisting of the splice site acceptor or donor consensus sequences of exon 45. In a preferred embodiment, such flanking sequences are complementary to sequences comprising or consisting of sequences of an intron of the DMD pre-mRNA which is adjacent to exon 45; i.e. intron 44 or 45.
A continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides within exon 45 is preferably selected from the sequence:

	(SEQ ID NO 2)
	5′-CCAGGAUGGCAUUGGGCAGCGGCAAACUGUUGUCAGA
	ACAUUGAAUGCAACUGGGGAAGAAAUAAUUCAGCAAUC-3′.

It was found that a molecule that binds to a nucleotide sequence comprising or consisting of a continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides of SEQ ID NO. 2 results in highly efficient skipping of exon 45 in a cell provided with this molecule. Molecules that bind to a nucleotide sequence comprising a continuous stretch of less than 21 nucleotides of SEQ ID NO:2 were found to induce exon skipping in a less efficient way than the molecules of the invention. Therefore, in a preferred embodiment, a method is provided wherein a molecule binds to a continuous stretch of at least 21, 25, 30, 35 nucleotides within SEQ ID NO:2. Contrary to what was generally thought, the inventors surprisingly found that a higher specificity and efficiency of exon skipping may be reached using an oligonucleotides having a length of at least 21 nucleotides. None of the indicated sequences is derived from conserved parts of splice-junction sites. Therefore, said molecule is not likely to mediate differential splicing of other exons from the DMD pre-mRNA or exons from other genes.
In one embodiment, a molecule of the invention capable of interfering with the inclusion of exon 45 of the DMD pre-mRNA is a compound molecule that binds to the specified sequence, or a protein such as an RNA-binding protein or a non-natural zinc-finger protein that has been modified to be able to bind to the indicated nucleotide sequence on a RNA molecule. Methods for screening compound molecules that bind specific nucleotide sequences are for example disclosed in PCT/NL01/00697 and US patent 6875736, which are herein enclosed by reference. Methods for designing RNA-binding Zinc-finger proteins that bind specific nucleotide sequences are disclosed by Friesen and Darby, Nature Structural Biology 5: 543-546 (1998) which is herein enclosed by reference.
In a further embodiment, a molecule of the invention capable of interfering with the inclusion of exon 45 of the DMD pre-mRNA comprises an antisense oligonucleotide that is complementary to and can base-pair with the coding strand of the pre-mRNA of the DMD gene. Said antisense oligonucleotide preferably contains a RNA residue, a DNA residue, and/or a nucleotide analogue or equivalent, as will be further detailed herein below.
A preferred molecule of the invention comprises a nucleotide-based or nucleotide or an antisense oligonucleotide sequence of between 21 and 50 nucleotides or bases, more preferred between 21 and 40 nucleotides, more preferred between 21 and 30 nucleotides, such as 21 nucleotides, 22 nucleotides, 23 nucleotides, 24 nucleotides, 25 nucleotides, 26 nucleotides, 27 nucleotides, 28 nucleotides, 29 nucleotides, 30 nucleotides, 31 nucleotides, 32 nucleotides, 33 nucleotides, 34 nucleotides, 35 nucleotides, 36 nucleotides, 37 nucleotides, 38 nucleotides, 39 nucleotides, 40 nucleotides, 41 nucleotides, 42 nucleotides, 43 nucleotides, 44 nucleotides, 45 nucleotides, 46 nucleotides, 47 nucleotides, 48 nucleotides, 49 nucleotides or 50 nucleotides.
A most preferred molecule of the invention comprises a nucleotide-based sequence of 25 nucleotides.
In a preferred embodiment, a molecule of the invention binds to a continuous stretch of or is complementary to or is antisense to at least a continuous stretch of at least 21 nucleotides within the nucleotide sequence SEQ ID NO:2.
In a certain embodiment, the invention provides a molecule comprising or consisting of an antisense nucleotide sequence selected from the antisense nucleotide sequences as depicted in Table 1, except SEQ ID NO:68. A molecule of the invention that is antisense to the sequence of SEQ ID NO 2, which is present in exon 45 of the DMD gene preferably comprises or consists of the antisense nucleotide sequence of SEQ ID NO 3; SEQ ID NO 4, SEQ ID NO 5, SEQ ID NO 6, SEQ ID NO 7, SEQ ID NO 8, SEQ ID NO 9, SEQ ID NO 10, SEQ ID NO 11, SEQ ID NO 12, SEQ ID NO 13, SEQ ID NO 14, SEQ ID NO 15, SEQ ID NO 16, SEQ ID NO 17, SEQ ID NO 18, SEQ ID NO 19, SEQ ID NO 20, SEQ ID NO 21, SEQ ID NO 22, SEQ ID NO 23, SEQ ID NO 24, SEQ ID NO 25, SEQ ID NO 26, SEQ ID NO 27, SEQ ID NO 28, SEQ ID NO 29, SEQ ID NO 30, SEQ ID NO 31, SEQ ID NO 32, SEQ ID NO 33, SEQ ID NO 34, SEQ ID NO 35, SEQ ID NO 36, SEQ ID NO 37, SEQ ID NO 38, SEQ ID NO 39, SEQ ID NO 40, SEQ ID NO 41, SEQ ID NO 42, SEQ ID NO 43, SEQ ID NO 44, SEQ ID NO 45, SEQ ID NO 46, SEQ ID NO 47, SEQ ID NO 48, SEQ ID NO 49, SEQ ID NO 50, SEQ ID NO 51, SEQ ID NO 52, SEQ ID NO 53, SEQ ID NO 54, SEQ ID NO 55, SEQ ID NO 56, SEQ ID NO 57, SEQ ID NO 58, SEQ ID NO 59, SEQ ID NO 60, SEQ ID NO 61, SEQ ID NO 62, SEQ ID NO 63, SEQ ID NO 64, SEQ ID NO 65, SEQ ID NO 66 and/or SEQ ID NO:67.
In a more preferred embodiment, the invention provides a molecule comprising or consisting of the antisense nucleotide sequence of SEQ ID NO 3; SEQ ID NO 4, SEQ ID NO 5, SEQ ID NO 6, SEQ ID NO 7 and/or SEQ ID NO 8.
In a most preferred embodiment, the invention provides a molecule comprising or consisting of the antisense nucleotide sequence of SEQ ID NO 3. It was found that this molecule is very efficient in modulating splicing of exon 45 of the DMD pre-mRNA in a muscle cell.
A nucleotide sequence of a molecule of the invention may contain a RNA residue, a DNA residue, a nucleotide analogue or equivalent as will be further detailed herein below. In addition, a molecule of the invention may encompass a functional equivalent of a molecule of the invention as defined herein.
It is preferred that a molecule of the invention comprises a or at least one residue that is modified to increase nuclease resistance, and/or to increase the affinity of the antisense nucleotide for the target sequence. Therefore, in a preferred embodiment, an antisense nucleotide sequence comprises a or at least one nucleotide analogue or equivalent, wherein a nucleotide analogue or equivalent is defined as a residue having a modified base, and/or a modified backbone, and/or a non-natural internucleoside linkage, or a combination of these modifications.
In a preferred embodiment, a nucleotide analogue or equivalent comprises a modified backbone. Examples of such backbones are provided by morpholino backbones, carbamate backbones, siloxane backbones, sulfide, sulfoxide and sulfone backbones, formacetyl and thioformacetyl backbones, methyleneformacetyl backbones, riboacetyl backbones, alkene containing backbones, sulfamate, sulfonate and sulfonamide backbones, methyleneimino and methylenehydrazino backbones, and amide backbones. Phosphorodiamidate morpholino oligomers are modified backbone oligonucleotides that have previously been investigated as antisense agents. Morpholino oligonucleotides have an uncharged backbone in which the deoxyribose sugar of DNA is replaced by a six membered ring and the phosphodiester linkage is replaced by a phosphorodiamidate linkage. Morpholino oligonucleotides are resistant to enzymatic degradation and appear to function as antisense agents by arresting translation or interfering with pre-mRNA splicing rather than by activating RNase H. Morpholino oligonucleotides have been successfully delivered to tissue culture cells by methods that physically disrupt the cell membrane, and one study comparing several of these methods found that scrape loading was the most efficient method of delivery; however, because the morpholino backbone is uncharged, cationic lipids are not effective mediators of morpholino oligonucleotide uptake in cells. A recent report demonstrated triplex formation by a morpholino oligonucleotide and, because of the non-ionic backbone, these studies showed that the morpholino oligonucleotide was capable of triplex formation in the absence of magnesium.
It is further preferred that the linkage between a residue in a backbone does not include a phosphorus atom, such as a linkage that is formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages.
A preferred nucleotide analogue or equivalent comprises a Peptide Nucleic Acid (PNA), having a modified polyamide backbone (Nielsen, et al. (1991) Science 254, 1497-1500). PNA-based molecules are true mimics of DNA molecules in terms of base-pair recognition. The backbone of the PNA is composed of N-(2-aminoethyl)-glycine units linked by peptide bonds, wherein the nucleobases are linked to the backbone by methylene carbonyl bonds. An alternative backbone comprises a one-carbon extended pyrrolidine PNA monomer (Govindaraju and Kumar (2005) Chem. Commun, 495-497). Since the backbone of a PNA molecule contains no charged phosphate groups, PNA-RNA hybrids are usually more stable than RNA-RNA or RNA-DNA hybrids, respectively (Egholm et al (1993) Nature 365, 566-568).
A further preferred backbone comprises a morpholino nucleotide analog or equivalent, in which the ribose or deoxyribose sugar is replaced by a 6-membered morpholino ring. A most preferred nucleotide analog or equivalent comprises a phosphorodiamidate morpholino oligomer (PMO), in which the ribose or deoxyribose sugar is replaced by a 6-membered morpholino ring, and the anionic phosphodiester linkage between adjacent morpholino rings is replaced by a non-ionic phosphorodiamidate linkage.
In yet a further embodiment, a nucleotide analogue or equivalent of the invention comprises a substitution of at least one of the non-bridging oxygens in the phosphodiester linkage. This modification slightly destabilizes base-pairing but adds significant resistance to nuclease degradation. A preferred nucleotide analogue or equivalent comprises phosphorothioate, chiral phosphorothioate, phosphorodithioate, phosphotriester, aminoalkylphosphotriester, H-phosphonate, methyl and other alkyl phosphonate including 3′-alkylene phosphonate, 5′-alkylene phosphonate and chiral phosphonate, phosphinate, phosphoramidate including 3′-amino phosphoramidate and aminoalkylphosphoramidate, thionophosphoramidate, thionoalkylphosphonate, thionoalkylphosphotriester, selenophosphate or boranophosphate.
A further preferred nucleotide analogue or equivalent of the invention comprises one or more sugar moieties that are mono- or disubstituted at the 2′, 3′ and/or 5′ position such as a —OH; —F; substituted or unsubstituted, linear or branched lower (C1-C10) alkyl, alkenyl, alkynyl, alkaryl, allyl, aryl, or aralkyl, that may be interrupted by one or more heteroatoms; O—, S—, or N-alkyl; O—, S—, or N-alkenyl; O—, S-or N-alkynyl; O—, S—, or N-allyl; O-alkyl-O-alkyl, -methoxy, -aminopropoxy; aminoxy, methoxyethoxy; -dimethylaminooxyethoxy; and -dimethylaminoethoxyethoxy. The sugar moiety can be a pyranose or derivative thereof, or a deoxypyranose or derivative thereof, preferably a ribose or a derivative thereof, or deoxyribose or derivative thereof. Such preferred derivatized sugar moieties comprise Locked Nucleic Acid (LNA), in which the 2′-carbon atom is linked to the 3′ or 4′ carbon atom of the sugar ring thereby forming a bicyclic sugar moiety. A preferred LNA comprises 2′-O,4′-C-ethylene-bridged nucleic acid (Morita et al. 2001. Nucleic Acid Res Supplement No. 1: 241-242). These substitutions render the nucleotide analogue or equivalent RNase H and nuclease resistant and increase the affinity for the target RNA.
It is understood by a skilled person that it is not necessary for all positions in an antisense oligonucleotide to be modified uniformly. In addition, more than one of the aforementioned analogues or equivalents may be incorporated in a single antisense oligonucleotide or even at a single position within an antisense oligonucleotide. In certain embodiments, an antisense oligonucleotide of the invention has at least two different types of analogues or equivalents.
A preferred antisense oligonucleotide according to the invention comprises a 2′-O -alkyl phosphorothioate antisense oligonucleotide, such as 2′-O-methyl modified ribose (RNA), 2′-O-ethyl modified ribose, 2′-O-propyl modified ribose, and/or substituted derivatives of these modifications such as halogenated derivatives.
A most preferred antisense oligonucleotide according to the invention comprises a 2′-O-methyl phosphorothioate ribose.
A functional equivalent of a molecule of the invention may be defined as an oligonucleotide as defined herein wherein an activity of said functional equivalent is retained to at least some extent. Preferably, an activity of said functional equivalent is inducing exon 45 skipping and providing a functional dystrophin protein. Said activity of said functional equivalent is therefore preferably assessed by detection of exon 45 skipping and quantifying the amount of a functional dystrophin protein. A functional dystrophin is herein preferably defined as being a dystrophin able to bind actin and members of the DGC protein complex. The assessment of said activity of an oligonucleotide is preferably done by RT-PCR or by immunofluorescence or Western blot analysis. Said activity is preferably retained to at least some extent when it represents at least 50%, or at least 60%, or at least 70% or at least 80% or at least 90% or at least 95% or more of corresponding activity of said oligonucleotide the functional equivalent derives from. Throughout this application, when the word oligonucleotide is used it may be replaced by a functional equivalent thereof as defined herein.
It will also be understood by a skilled person that distinct antisense oligonucleotides can be combined for efficiently skipping of exon 45 of the human DMD pre-mRNA. In a preferred embodiment, a combination of at least two antisense oligonucleotides are used in a method of the invention, such as two distinct antisense oligonucleotides, three distinct antisense oligonucleotides, four distinct antisense oligonucleotides, or five distinct antisense oligonucleotides or even more. It is also encompassed by the present invention to combine several oligonucleotides or molecules as depicted in table 1 except SEQ ID NO:68.
An antisense oligonucleotide can be linked to a moiety that enhances uptake of the antisense oligonucleotide in cells, preferably myogenic cells or muscle cells. Examples of such moieties are cholesterols, carbohydrates, vitamins, biotin, lipids, phospholipids, cell-penetrating peptides including but not limited to antennapedia, TAT, transportan and positively charged amino acids such as oligoarginine, poly-arginine, oligolysine or polylysine, antigen-binding domains such as provided by an antibody, a Fab fragment of an antibody, or a single chain antigen binding domain such as a cameloid single domain antigen-binding domain.
A preferred antisense oligonucleotide comprises a peptide-linked PMO.
A preferred antisense oligonucleotide comprising one or more nucleotide analogs or equivalents of the invention modulates splicing in one or more muscle cells, including heart muscle cells, upon systemic delivery. In this respect, systemic delivery of an antisense oligonucleotide comprising a specific nucleotide analog or equivalent might result in targeting a subset of muscle cells, while an antisense oligonucleotide comprising a distinct nucleotide analog or equivalent might result in targeting of a different subset of muscle cells. Therefore, in one embodiment it is preferred to use a combination of antisense oligonucleotides comprising different nucleotide analogs or equivalents for modulating skipping of exon 45 of the human DMD pre-mRNA.
A cell can be provided with a molecule capable of interfering with essential sequences that result in highly efficient skipping of exon 45 of the human DMD pre-mRNA by plasmid-derived antisense oligonucleotide expression or viral expression provided by viral-based vector. Such a viral-based vector comprises an expression cassette that drives expression of an antisense molecule as defined herein. Preferred virus-based vectors include adenovirus- or adeno-associated virus-based vectors. Expression is preferably driven by a polymerase III promoter, such as a U1, a U6, or a U7 RNA promoter. A muscle or myogenic cell can be provided with a plasmid for antisense oligonucleotide expression by providing the plasmid in an aqueous solution. Alternatively, a plasmid can be provided by transfection using known transfection agentia such as, for example, LipofectAMINETM 2000 (Invitrogen) or polyethyleneimine (PEI; ExGen500 (MBI Fermentas)), or derivatives thereof.
One preferred antisense oligonucleotide expression system is an adenovirus associated virus (AAV)-based vector. Single chain and double chain AAV-based vectors have been developed that can be used for prolonged expression of small antisense nucleotide sequences for highly efficient skipping of exon 45 of the DMD pre-mRNA.
A preferred AAV-based vector comprises an expression cassette that is driven by a polymerase III-promoter (Pol III). A preferred Pol III promoter is, for example, a U1, a U6, or a U7 RNA promoter.
The invention therefore also provides a viral-based vector, comprising a Pol III-promoter driven expression cassette for expression of one or more antisense sequences of the invention for inducing skipping of exon 45 of the human DMD pre-mRNA.

Pharmaceutical Composition

If required, a molecule or a vector expressing an antisense oligonucleotide of the invention can be incorporated into a pharmaceutically active mixture or composition by adding a pharmaceutically acceptable carrier.
Therefore, in a further aspect, the invention provides a composition, preferably a pharmaceutical composition comprising a molecule comprising an antisense oligonucleotide according to the invention, and/or a viral-based vector expressing the antisense sequence(s) according to the invention and a pharmaceutically acceptable carrier.
A preferred pharmaceutical composition comprises a molecule as defined herein and/or a vector as defined herein, and a pharmaceutical acceptable carrier or excipient, optionally combined with a molecule and/or a vector which is able to modulate skipping of exon 7, 44, 46, 51, 53, 59, 67 of the DMD pre-mRNA.
Preferred excipients include excipients capable of forming complexes, vesicles and/or liposomes that deliver such a molecule as defined herein, preferably an oligonucleotide complexed or trapped in a vesicle or liposome through a cell membrane. Many of these excipients are known in the art. Suitable excipients comprise polyethylenimine and derivatives, or similar cationic polymers, including polypropyleneimine or polyethylenimine copolymers (PECs) and derivatives, synthetic amphiphils, lipofectin™, DOTAP and/or viral capsid proteins that are capable of self assembly into particles that can deliver such molecule, preferably an oligonucleotide as defined herein to a cell, preferably a muscle cell. Such excipients have been shown to efficiently deliver (oligonucleotide such as antisense) nucleic acids to a wide variety of cultured cells, including muscle cells. We obtained very good results using polyethylenimine (PEI, ExGen500, MBI Fermentas) as shown in the example. Their high transfection potential is combined with an excepted low to moderate toxicity in terms of overall cell survival. The ease of structural modification can be used to allow further modifications and the analysis of their further (in vivo) nucleic acid transfer characteristics and toxicity.
Lipofectin represents an example of a liposomal transfection agent. It consists of two lipid components, a cationic lipid N-[1-(2,3 dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) (cp. DOTAP which is the methylsulfate salt) and a neutral lipid dioleoylphosphatidylethanolamine (DOPE). The neutral component mediates the intracellular release. Another group of delivery systems are polymeric nanoparticles.
Polycations such like diethylaminoethylaminoethyl (DEAE)-dextran, which are well known as DNA transfection reagent can be combined with butylcyanoacrylate (PBCA) and hexylcyanoacrylate (PHCA) to formulate cationic nanoparticles that can deliver a molecule or a compound as defined herein, preferably an oligonucleotide across cell membranes into cells.
In addition to these common nanoparticle materials, the cationic peptide protamine offers an alternative approach to formulate a compound as defined herein, preferably an oligonucleotide as colloids. This colloidal nanoparticle system can form so called proticles, which can be prepared by a simple self-assembly process to package and mediate intracellular release of a compound as defined herein, preferably an oligonucleotide. The skilled person may select and adapt any of the above or other commercially available alternative excipients and delivery systems to package and deliver a compound as defined herein, preferably an oligonucleotide for use in the current invention to deliver said compound for the treatment of Duchenne Muscular Dystrophy in humans.
In addition, a compound as defined herein, preferably an oligonucleotide could be covalently or non-covalently linked to a targeting ligand specifically designed to facilitate the uptake in to the cell, cytoplasm and/or its nucleus. Such ligand could comprise (i) a compound (including but not limited to peptide(-like) structures) recognising cell, tissue or organ specific elements facilitating cellular uptake and/or (ii) a chemical compound able to facilitate the uptake in to cells and/or the intracellular release of an a compound as defined herein, preferably an oligonucleotide from vesicles, e.g. endosomes or lysosomes.
Therefore, in a preferred embodiment, a compound as defined herein, preferably an oligonucleotide are formulated in a medicament which is provided with at least an excipient and/or a targeting ligand for delivery and/or a delivery device of said compound to a cell and/or enhancing its intracellular delivery. Accordingly, the invention also encompasses a pharmaceutically acceptable composition comprising a compound as defined herein, preferably an oligonucleotide and further comprising at least one excipient and/or a targeting ligand for delivery and/or a delivery device of said compound to a cell and/or enhancing its intracellular delivery.
It is to be understood that a molecule or compound or oligonucleotide may not be formulated in one single composition or preparation. Depending on their identity, the skilled person will know which type of formulation is the most appropriate for each compound.
In a preferred embodiment, an in vitro concentration of a molecule or an oligonucleotide as defined herein, which is ranged between 0.1 nM and 1 μM is used. More preferably, the concentration used is ranged between 0.3 to 400 nM, even more preferably between 1 to 200 nM. molecule or an oligonucleotide as defined herein may be used at a dose which is ranged between 0.1 and 20 mg/kg, preferably 0.5 and 10 mg/kg. If several molecules or oligonucleotides are used, these concentrations may refer to the total concentration of oligonucleotides or the concentration of each oligonucleotide added. The ranges of concentration of oligonucleotide(s) as given above are preferred concentrations for in vitro or ex vivo uses. The skilled person will understand that depending on the oligonucleotide(s) used, the target cell to be treated, the gene target and its expression levels, the medium used and the transfection and incubation conditions, the concentration of oligonucleotide(s) used may further vary and may need to be optimised any further.
More preferably, a compound preferably an oligonucleotide and an adjunct compound to be used in the invention to prevent, treat DMD are synthetically produced and administered directly to a cell, a tissue, an organ and/or patients in formulated form in a pharmaceutically acceptable composition or preparation. The delivery of a pharmaceutical composition to the subject is preferably carried out by one or more parenteral injections, e.g. intravenous and/or subcutaneous and/or intramuscular and/or intrathecal and/or intraventricular administrations, preferably injections, at one or at multiple sites in the human body.

Use

In yet a further aspect, the invention provides the use of an antisense oligonucleotide or molecule according to the invention, and/or a viral-based vector that expresses one or more antisense sequences according to the invention and/or a pharmaceutical composition, for inducing and/or promoting splicing of the DMD pre-mRNA. The splicing is preferably modulated in a human myogenic cell or a muscle cell in vitro. More preferred is that splicing is modulated in human a myogenic cell or muscle cell in vivo.
Accordingly, the invention further relates to the use of the molecule as defined herein and/or the vector as defined herein and/or or the pharmaceutical composition as defined herein for inducing and/or promoting splicing of the DMD pre-mRNA or for the preparation of a medicament for the treatment of a DMD patient.
In this document and in its claims, the verb “to comprise” and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. In addition the verb “to consist” may be replaced by “to consist essentially of” meaning that a molecule or a viral-based vector or a composition as defined herein may comprise additional component(s) than the ones specifically identified, said additional component(s) not altering the unique characteristic of the invention. In addition, reference to an element by the indefinite article “a” or “an” does not exclude the possibility that more than one of the element is present, unless the context clearly requires that there be one and only one of the elements. The indefinite article “a” or “an” thus usually means “at least one”.
Each embodiment as identified herein may be combined together unless otherwise indicated. All patent and literature references cited in the present specification are hereby incorporated by reference in their entirety.
The following examples are offered for illustrative purposes only, and are not intended to limit the scope of the present invention in any way.

LEGENDS TO THE FIGURE

FIG. 1. In human control myotubes, a series of AONs (PS220 to PS225; SEQ ID NO: 3 to 8), all binding to a continuous stretch of at least 21 nucleotides within a specific sequence of exon 45 (i.e. SEQ ID NO:2), were tested at two different concentrations (200 and 500 nM). All six AONs were effective in inducing specific exon 45 skipping, as confirmed by sequence analysis (not shown). PS220 (SEQ ID NO:3) however, reproducibly induced highest levels of exon 45 skipping (see FIG. 2). (NT: non-treated cells, M: size marker).

FIG. 2. In human control myotubes, 25-mer PS220 (SEQ ID NO: 3) was tested at increasing concentration. Levels of exon 45 skipping of up to 75% (at 400 nM) were observed reproducibly, as assessed by Agilent LabChip Analysis.

FIG. 3. In human control myotubes, the efficiencies of a “short” 17-mer AON45-5 (SEQ ID NO:68) and its overlapping “long” 25-mer counterpart PS220 were directly compared at 200 nM and 500 nM. PS220 was markedly more efficient at both concentrations: 63% when compared to 3% obtained with 45-5. (NT: non-treated cells, M: size marker).

EXAMPLES

Examples 1 and 2

Materials and Methods
AON design was based on (partly) overlapping open secondary structures of the target exon RNA as predicted by the m-fold program (Zuker,M. (2003) Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res., 31, 3406-3415), and on (partly) overlapping putative SR-protein binding sites as predicted by numerous software programs such as ESEfinder (Cartegni,L. et al.(2003) ESEfinder: A web resource to identify exonic splicing enhancers. Nucleic Acids Res, 31, 3568-71; Smith,P. J. et al. (2006) An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers. Hum.Mol.Genet., 15, 2490-2508) that predicts binding sites for the four most abundant SR proteins (SF2/ASF, SC35, SRp40 and SRp55). AONs were synthesized by Prosensa Therapeutics B. V. (Leiden, Netherlands), and contain 2′-O-methyl RNA and full-length phosphorothioate (PS) backbones.
Tissue culturing, transfection and RT-PCR analysis Myotube cultures derived from a healthy individual (“human control”) were obtained as described previously (Aartsma-Rus et al. Hum Mol Genet 2003; 12(8): 907-14). For the screening of AONs, myotube cultures were transfected with 0 to 500 nM of each AON. The transfection reagent polyethylenimine (PEI, ExGen500 MBI Fermentas) was used according to manufacturer's instructions, with 2 μl PEI per μg AON. Exon skipping efficiencies were determined by nested RT-PCR analysis using primers in the exons flanking exon 45. PCR fragments were isolated from agarose gels for sequence verification. For quantification, the PCR products were analyzed using the Agilent DNA 1000 LabChip Kit and the Agilent 2100 bioanalyzer (Agilent Technologies, USA).
Results
A series of AONs targeting sequences within SEQ ID NO:2 within exon 45 were designed and tested in normal myotube cultures, by transfection and subsequent RT-PCR and sequence analysis of isolated RNA. PS220 (SEQ ID NO: 3) reproducibly induced highest levels of exon 45 skipping, when compared to PS221-PS225 (FIG. 1). High levels of exon 45 skipping of up to 75% were already obtained at 400 nM PS220 (FIG. 2). In a direct comparison, PS220 (a 25-mer) was reproducibly more efficient in inducing exon 45 skipping than its shorter 17-mer counterpart AON 45-5 (SEQ ID NO: 68; previously published as h45AON5 (Aartsma-Rus et al. Am J Hum Genet 2004;74: 83-92)), at both AON concentrations of 200 nM and 500 nM and with 63% versus 3% respectively at 500 nM (FIG. 3). This result is probably due to the fact that the extended length of PS220, in fact completely overlapping AON 45-5, increases the free energy of the AON-target complex such that the efficiency of inducing exon 45 skipping is also increased.

TABLE 1

AONs in exon 45

SEQ ID NO 3	UUUGCCGCUGCCCAAUGCCAUCCUG	SEQ ID NO 36	GUUGCAUUCAAUGUUCUGACAACAG
(PS220)

SEQ ID NO 4	AUUCAAUGUUCUGACAACAGUUUGC	SEQ ID NO 37	UUGCAUUCAAUGUUCUGACAACAGU
(PS221)

SEQ ID NO 5	CCAGUUGCAUUCAAUGUUCUGACAA	SEQ ID NO 38	UGCAUUCAAUGUUCUGACAACAGUU
(PS222)

SEQ ID NO 6	CAGUUGCAUUCAAUGUUCUGAC	SEQ ID NO 39	GCAUUCAAUGUUCUGACAACAGUUU
(PS223)

SEQ ID NO 7	AGUUGCAUUCAAUGUUCUGA	SEQ ID NO 40	CAUUCAAUGUUCUGACAACAGUUUG
(PS224)

SEQ ID NO 8	GAUUGCUGAAUUAUUUCUUCC	SEQ ID NO 41	AUUCAAUGUUCUGACAACAGUUUGC
(PS225)

SEQ ID NO 9	GAUUGCUGAAUUAUUUCUUCCCCAG	SEQ ID NO 42	UCAAUGUUCUGACAACAGUUUGCCG

SEQ ID NO 10	AUUGCUGAAUUAUUUCUUCCCCAGU	SEQ ID NO 43	CAAUGUUCUGACAACAGUUUGCCGC

SEQ ID NO 11	UUGCUGAAUUAUUUCUUCCCCAGUU	SEQ ID NO 44	AAUGUUCUGACAACAGUUUGCCGCU

SEQ ID NO 12	UGCUGAAUUAUUUCUUCCCCAGUUG	SEQ ID NO 45	AUGUUCUGACAACAGUUUGCCGCUG

SEQ ID NO 13	GCUGAAUUAUUUCUUCCCCAGUUGC	SEQ ID NO 46	UGUUCUGACAACAGUUUGCCGCUGC

SEQ ID NO 14	CUGAAUUAUUUCUUCCCCAGUUGCA	SEQ ID NO 47	GUUCUGACAACAGUUUGCCGCUGCC

SEQ ID NO 15	UGAAUUAUUUCUUCCCCAGUUGCAU	SEQ ID NO 48	UUCUGACAACAGUUUGCCGCUGCCC

SEQ ID NO 16	GAAUUAUUUCUUCCCCAGUUGCAUU	SEQ ID NO 49	UCUGACAACAGUUUGCCGCUGCCCA

SEQ ID NO 17	AAUUAUUUCUUCCCCAGUUGCAUUC	SEQ ID NO 50	CUGACAACAGUUUGCCGCUGCCCAA

SEQ ID NO 18	AUUAUUUCUUCCCCAGUUGCAUUCA	SEQ ID NO 51	UGACAACAGUUUGCCGCUGCCCAAU

SEQ ID NO 19	UUAUUUCUUCCCCAGUUGCAUUCAA	SEQ ID NO 52	GACAACAGUUUGCCGCUGCCCAAUG

SEQ ID NO 20	UAUUUCUUCCCCAGUUGCAUUCAAU	SEQ ID NO 53	ACAACAGUUUGCCGCUGCCCAAUGC

SEQ ID NO 21	AUUUCUUCCCCAGUUGCAUUCAAUG	SEQ ID NO 54	CAACAGUUUGCCGCUGCCCAAUGCC

SEQ ID NO 22	UUUCUUCCCCAGUUGCAUUCAAUGU	SEQ ID NO 55	AACAGUUUGCCGCUGCCCAAUGCCA

SEQ ID NO 23	UUCUUCCCCAGUUGCAUUCAAUGUU	SEQ ID NO 56	ACAGUUUGCCGCUGCCCAAUGCCAU

SEQ ID NO 24	UCUUCCCCAGUUGCAUUCAAUGUUC	SEQ ID NO 57	CAGUUUGCCGCUGCCCAAUGCCAUC

SEQ ID NO 25	CUUCCCCAGUUGCAUUCAAUGUUCU	SEQ ID NO 58	AGUUUGCCGCUGCCCAAUGCCAUCC

SEQ ID NO 26	UUCCCCAGUUGCAUUCAAUGUUCUG	SEQ ID NO 59	GUUUGCCGCUGCCCAAUGCCAUCCU

SEQ ID NO 27	UCCCCAGUUGCAUUCAAUGUUCUGA	SEQ ID NO 60	UUUGCCGCUGCCCAAUGCCAUCCUG

SEQ ID NO 28	CCCCAGUUGCAUUCAAUGUUCUGAC	SEQ ID NO 61	UUGCCGCUGCCCAAUGCCAUCCUGG

SEQ ID NO 29	CCCAGUUGCAUUCAAUGUUCUGACA	SEQ ID NO 62	UGCCGCUGCCCAAUGCCAUCCUGGA

SEQ ID NO 30	CCAGUUGCAUUCAAUGUUCUGACAA	SEQ ID NO 63	GCCGCUGCCCAAUGCCAUCCUGGAG

SEQ ID NO 31	CAGUUGCAUUCAAUGUUCUGACAAC	SEQ ID NO 64	CCGCUGCCCAAUGCCAUCCUGGAGU

SEQ ID NO 32	AGUUGCAUUCAAUGUUCUGACAACA	SEQ ID NO 65	CGCUGCCCAAUGCCAUCCUGGAGUU

SEQ ID NO 33	UCC UGU AGA AUA CUG GCA UC	SEQ ID NO 66	UGU UUU UGA GGA UUG CUG AA

SEQ ID NO 34	UGC AGA CCU CCU GCC ACC GCA	SEQ ID NO 67	UGUUCUGACAACAGUUUGCCGCUGCCCAAU
	GAU UCA		GCCAUCCUGG

SEQ ID NO 35	UUGCAGACCUCCUGCCACCGCAGAUUC	SEQ ID NO 68	GCCCAAUGCCAUCCUGG
	AGGCUUC	(45-5)

TABLE 2

AONs in exons 51, 53, 7, 44, 46, 59, and 67

DMD Gene Exon 51

SEQ ID NO 69	AGAGCAGGUACCUCCAACAUCAAGG	SEQ ID NO 91	UCAAGGAAGAUGGCAUUUCUAGUUU
SEQ ID NO 70	GAGCAGGUACCUCCAACAUCAAGGA	SEQ ID NO 92	UCAAGGAAGAUGGCAUUUCU
SEQ ID NO 71	AGCAGGUACCUCCAACAUCAAGGAA	SEQ ID NO 93	CAAGGAAGAUGGCAUUUCUAGUUUG
SEQ ID NO 72	GCAGGUACCUCCAACAUCAAGGAAG	SEQ ID NO 94	AAGGAAGAUGGCAUUUCUAGUUUGG
SEQ ID NO 73	CAGGUACCUCCAACAUCAAGGAAGA	SEQ ID NO 95	AGGAAGAUGGCAUUUCUAGUUUGGA
SEQ ID NO 74	AGGUACCUCCAACAUCAAGGAAGAU	SEQ ID NO 96	GGAAGAUGGCAUUUCUAGUUUGGAG
SEQ ID NO 75	GGUACCUCCAACAUCAAGGAAGAUG	SEQ ID NO 97	GAAGAUGGCAUUUCUAGUUUGGAGA
SEQ ID NO 76	GUACCUCCAACAUCAAGGAAGAUGG	SEQ ID NO 98	AAGAUGGCAUUUCUAGUUUGGAGAU
SEQ ID NO 77	UACCUCCAACAUCAAGGAAGAUGGC	SEQ ID NO 99	AGAUGGCAUUUCUAGUUUGGAGAUG
SEQ ID NO 78	ACCUCCAACAUCAAGGAAGAUGGCA	SEQ ID NO 100	GAUGGCAUUUCUAGUUUGGAGAUGG
SEQ ID NO 79	CCUCCAACAUCAAGGAAGAUGGCAU	SEQ ID NO 101	AUGGCAUUUCUAGUUUGGAGAUGGC
SEQ ID NO 80	CUCCAACAUCAAGGAAGAUGGCAUU	SEQ ID NO 102	UGGCAUUUCUAGUUUGGAGAUGGCA
SEQ ID NO 81	CUCCAACAUCAAGGAAGAUGGCAUUUCUAG	SEQ ID NO 103	GGCAUUUCUAGUUUGGAGAUGGCAG
SEQ ID NO 82	UCCAACAUCAAGGAAGAUGGCAUUU	SEQ ID NO 104	GCAUUUCUAGUUUGGAGAUGGCAGU
SEQ ID NO 83	CCAACAUCAAGGAAGAUGGCAUUUC	SEQ ID NO 105	CAUUUCUAGUUUGGAGAUGGCAGUU
SEQ ID NO 84	CAACAUCAAGGAAGAUGGCAUUUCU	SEQ ID NO 106	AUUUCUAGUUUGGAGAUGGCAGUUU
SEQ ID NO 85	AACAUCAAGGAAGAUGGCAUUUCUA	SEQ ID NO 107	UUUCUAGUUUGGAGAUGGCAGUUUC
SEQ ID NO 86	ACAUCAAGGAAGAUGGCAUUUCUAG	SEQ ID NO 108	UUCUAGUUUGGAGAUGGCAGUUUCC
SEQ ID NO 87	ACAUCAAGGAAGAUGGCAUUUCUAGUUUGG
SEQ ID NO 88	ACAUCAAGGAAGAUGGCAUUUCUAG
SEQ ID NO 89	CAUCAAGGAAGAUGGCAUUUCUAGU
SEQ ID NO 90	AUCAAGGAAGAUGGCAUUUCUAGUU

DMD Gene Exon 53

SEQ ID NO 109	CCAUUGUGUUGAAUCCUUUAACAUU	SEQ ID NO 116	CAUUCAACUGUUGCCUCCGGUUCUGAAGGUG
SEQ ID NO 110	CCAUUGUGUUGAAUCCUUUAAC	SEQ ID NO 117	CUGAAGGUGUUCUUGUACUUCAUCC
SEQ ID NO 111	AUUGUGUUGAAUCCUUUAAC	SEQ ID NO 118	UGUAUAGGGACCCUCCUUCCAUGACUC
SEQ ID NO 112	CCUGUCCUAAGACCUGCUCA	SEQ ID NO 119	AUCCCACUGAUUCUGAAUUC
SEQ ID NO 113	CUUUUGGAUUGCAUCUACUGUAUAG	SEQ ID NO 120	UUGGCUCUGGCCUGUCCUAAGA
SEQ ID NO 114	CAUUCAACUGUUGCCUCCGGUUCUG	SEQ ID NO 121	AAGACCUGCUCAGCUUCUUCCUUAGCUUCCAGCCA
SEQ ID NO 115	CUGUUGCCUCCGGUUCUGAAGGUG

DMD Gene Exon 7

SEQ ID NO 122	UGCAUGUUCCAGUCGUUGUGUGG	SEQ ID NO 124	AUUUACCAACCUUCAGGAUCGAGUA
SEQ ID NO 123	CACUAUUCCAGUCAAAUAGGUCUGG	SEQ ID NO 125	GGCCUAAAACACAUACACAUA

DMD Gene Exon 44

SEQ ID NO 126	UCAGCUUCUGUUAGCCACUG	SEQ ID NO 151	AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 127	UUCAGCUUCUGUUAGCCACU	SEQ ID NO 152	CAGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 128	UUCAGCUUCUGUUAGCCACUG	SEQ ID NO 153	AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 129	UCAGCUUCUGUUAGCCACUGA	SEQ ID NO 154	AGCUUCUGUUAGCCACUGAU
SEQ ID NO 130	UUCAGCUUCUGUUAGCCACUGA	SEQ ID NO 155	GCUUCUGUUAGCCACUGAUU
SEQ ID NO 131	UCAGCUUCUGUUAGCCACUGA	SEQ ID NO 156	AGCUUCUGUUAGCCACUGAUU
SEQ ID NO 132	UUCAGCUUCUGUUAGCCACUGA	SEQ ID NO 157	GCUUCUGUUAGCCACUGAUUA
SEQ ID NO 133	UCAGCUUCUGUUAGCCACUGAU	SEQ ID NO 158	AGCUUCUGUUAGCCACUGAUUA
SEQ ID NO 134	UUCAGCUUCUGUUAGCCACUGAU	SEQ ID NO 159	GCUUCUGUUAGCCACUGAUUAA
SEQ ID NO 135	UCAGCUUCUGUUAGCCACUGAUU	SEQ ID NO 160	AGCUUCUGUUAGCCACUGAUUAA
SEQ ID NO 136	UUCAGCUUCUGUUAGCCACUGAUU	SEQ ID NO 161	GCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 137	UCAGCUUCUGUUAGCCACUGAUUA	SEQ ID NO 162	AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 138	UUCAGCUUCUGUUAGCCACUGAUA	SEQ ID NO 163	GCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 139	UCAGCUUCUGUUAGCCACUGAUUAA	SEQ ID NO 164	CCAUUUGUAUUUAGCAUGUUCCC
SEQ ID NO 140	UUCAGCUUCUGUUAGCCACUGAUUAA	SEQ ID NO 165	AGAUACCAUUUGUAUUUAGC
SEQ ID NO 141	UCAGCUUCUGUUAGCCACUGAUUAAA	SEQ ID NO 166	GCCAUUUCUCAACAGAUCU
SEQ ID NO 142	UUCAGCUUCUGUUAGCCACUGAUUAAA	SEQ ID NO 167	GCCAUUUCUCAACAGAUCUGUCA
SEQ ID NO 143	CAGCUUCUGUUAGCCACUG	SEQ ID NO 168	AUUCUCAGGAAUUUGUGUCUUUC
SEQ ID NO 144	CAGCUUCUGUUAGCCACUGAU	SEQ ID NO 169	UCUCAGGAAUUUGUGUCUUUC
SEQ ID NO 145	AGCUUCUGUUAGCCACUGAUU	SEQ ID NO 170	GUUCAGCUUCUGUUAGCC
SEQ ID NO 146	CAGCUUCUGUUAGCCACUGAUU	SEQ ID NO 171	CUGAUUAAAUAUCUUUAUAU C
SEQ ID NO 147	AGCUUCUGUUAGCCACUGAUUA	SEQ ID NO 172	GCCGCCAUUUCUCAACAG
SEQ ID NO 148	CAGCUUCUGUUAGCCACUGAUUA	SEQ ID NO 173	GUAUUUAGCAUGUUCCCA
SEQ ID NO 149	AGCUUCUGUUAGCCACUGAUUAA	SEQ ID NO 174	CAGGAAUUUGUGUCUUUC
SEQ ID NO 150	CAGCUUCUGUUAGCCACUGAUUAA

DMD Gene Exon 46

SEQ ID NO 175	GCUUUUCUUUUAGUUGCUGCUCUUU	SEQ ID NO 203	AGGUUCAAGUGGGAUACUAGCAAUG
SEQ ID NO 176	CUUUUCUUUUAGUUGCUGCUCUUUU	SEQ ID NO 204	GGUUCAAGUGGGAUACUAGCAAUGU
SEQ ID NO 177	UUUUCUUUUAGUUGCUGCUCUUUUC	SEQ ID NO 205	GUUCAAGUGGGAUACUAGCAAUGUU
SEQ ID NO 178	UUUCUUUUAGUUGCUGCUCUUUUCC	SEQ ID NO 206	UUCAAGUGGGAUACUAGCAAUGUUA
SEQ ID NO 179	UUCUUUUAGUUGCUGCUCUUUUCCA	SEQ ID NO 207	UCAAGUGGGAUACUAGCAAUGUUAU
SEQ ID NO 180	UCUUUUAGUUGCUGCUCUUUUCCAG	SEQ ID NO 208	CAAGUGGGAUACUAGCAAUGUUAUC
SEQ ID NO 181	CUUUUAGUUGCUGCUCUUUUCCAGG	SEQ ID NO 209	AAGUGGGAUACUAGCAAUGUUAUCU
SEQ ID NO 182	UUUUAGUUGCUGCUCUUUUCCAGGU	SEQ ID NO 210	AGUGGGAUACUAGCAAUGUUAUCUG
SEQ ID NO 183	UUUAGUUGCUGCUCUUUUCCAGGUU	SEQ ID NO 211	GUGGGAUACUAGCAAUGUUAUCUGC
SEQ ID NO 184	UUAGUUGCUGCUCUUUUCCAGGUUC	SEQ ID NO 212	UGGGAUACUAGCAAUGUUAUCUGCU
SEQ ID NO 185	UAGUUGCUGCUCUUUUCCAGGUUCA	SEQ ID NO 213	GGGAUACUAGCAAUGUUAUCUGCUU
SEQ ID NO 186	AGUUGCUGCUCUUUUCCAGGUUCAA	SEQ ID NO 214	GGAUACUAGCAAUGUUAUCUGCUUC
SEQ ID NO 187	GUUGCUGCUCUUUUCCAGGUUCAAG	SEQ ID NO 215	GAUACUAGCAAUGUUAUCUGCUUCC
SEQ ID NO 188	UUGCUGCUCUUUUCCAGGUUCAAGU	SEQ ID NO 216	AUACUAGCAAUGUUAUCUGCUUCCU
SEQ ID NO 189	UGCUGCUCUUUUCCAGGUUCAAGUG	SEQ ID NO 217	UACUAGCAAUGUUAUCUGCUUCCUC
SEQ ID NO 190	GCUGCUCUUUUCCAGGUUCAAGUGG	SEQ ID NO 218	ACUAGCAAUGUUAUCUGCUUCCUCC
SEQ ID NO 191	CUGCUCUUUUCCAGGUUCAAGUGGG	SEQ ID NO 219	CUAGCAAUGUUAUCUGCUUCCUCCA
SEQ ID NO 192	UGCUCUUUUCCAGGUUCAAGUGGGA	SEQ ID NO 220	UAGCAAUGUUAUCUGCUUCCUCCAA
SEQ ID NO 193	GCUCUUUUCCAGGUUCAAGUGGGAC	SEQ ID NO 221	AGCAAUGUUAUCUGCUUCCUCCAAC
SEQ ID NO 194	CUCUUUUCCAGGUUCAAGUGGGAUA	SEQ ID NO 222	GCAAUGUUAUCUGCUUCCUCCAACC
SEQ ID NO 195	UCUUUUCCAGGUUCAAGUGGGAUAC	SEQ ID NO 223	CAAUGUUAUCUGCUUCCUCCAACCA
SEQ ID NO 196	CUUUUCCAGGUUCAAGUGGGAUACU	SEQ ID NO 224	AAUGUUAUCUGCUUCCUCCAACCAU
SEQ ID NO 197	UUUUCCAGGUUCAAGUGGGAUACUA	SEQ ID NO 225	AUGUUAUCUGCUUCCUCCAACCAUA
SEQ ID NO 198	UUUCCAGGUUCAAGUGGGAUACUAG	SEQ ID NO 226	UGUUAUCUGCUUCCUCCAACCAUAA
SEQ ID NO 199	UUCCAGGUUCAAGUGGGAUACUAGC	SEQ ID NO 227	GUUAUCUGCUUCCUCCAACCAUAAA
SEQ ID NO 200	UCCAGGUUCAAGUGGGAUACUAGCA	SEQ ID NO 228	GCUGCUCUUUUCCAGGUUC
SEQ ID NO 201	CCAGGUUCAAGUGGGAUACUAGCAA	SEQ ID NO 229	UCUUUUCCAGGUUCAAGUGG
SEQ ID NO 202	CAGGUUCAAGUGGGAUACUAGCAAU	SEQ ID NO 230	AGGUUCAAGUGGGAUACUA

DMD Gene Exon 59

SEQ ID NO 231	CAAUUUUUCCCACUCAGUAUU	SEQ ID NO 233	UCCUCAGGAGGCAGCUCUAAAU
SEQ ID NO 232	UUGAAGUUCCUGGAGUCUU

DMD Gene Exon 67

SEQ ID NO 234	GCGCUGGUCACAAAAUCCUGUUGAAC	SEQ ID NO 236	GGUGAAUAACUUACAAAUUUGGAAGC
SEQ ID NO 235	CACUUGCUUGAAAAGGUCUACAAAGGA

Claims

1-15. (canceled)

16. An antisense oligonucleotide of 25 nucleotides in length, wherein the antisense oligonucleotide comprises at least 18 consecutive bases of a base sequence of the sequence CUGUUGCCUCCGGUUCUGAAGGUG (SEQ ID NO: 115), in which uracil bases are thymine bases, wherein the antisense oligonucleotide is a morpholino phosphorodiamidate antisense oligonucleotide, and wherein the antisense oligonucleotide induces exon 53 skipping of human dystrophin pre-mRNA.

17. A pharmaceutical composition, comprising the oligonucleotide of claim 16 and a pharmaceutically acceptable excipient.

18. A method for treating Duchenne Muscular Dystrophy (DMD) or Becker Muscular Dystrophy (BMD), comprising administering to a subject a therapeutically effective amount of the oligonucleotide of claim 16.