IP Library Granted Patent US 10,947,540
Granted Patent B2
US 10,947,540 · App. 16/464,482 · Granted Mar 16, 2021

Allele-specific silencing therapy for Dynamin 2-related diseases

Inventors: Marc Bitoun (Villejuif, FR); Delphine Trochet (Villejuif, FR); Bernard Prudhon (Paris, FR)
Assignees: ASSOCIATION INSTITUT DE MYOLOGIE; INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE; SORBONNE UNIVERSITE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
C12N15/1137C12N2310/14C12N2320/34C12Y306/05005
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Quick Facts
Patent No.
US 10,947,540
App. No.
16/464,482
Granted
Mar 16, 2021
Kind
B2
Abstract

The invention relates to an allele specific siRNA able to silence the expression of only one allele of a heterozygous DNM2 gene, for treating diseases caused by heterozygous mutation and/or overexpression of Dynamin 2.

Claims (14)

1. An allele specific siRNA (AS-siRNA) that comprises a sequence mismatch and is able to silence the expression of only one allele of a heterozygous DNM2 gene in a cell, wherein the DNM2 gene is heterozygous for the presence of a non-pathological polymorphism, wherein the non-pathological polymorphism is rs2229920 (C or T) or rs12461992 (A or T), and wherein the AS-siRNA targets a region of the allele comprising said non-pathological polymorphism.

2. The AS-siRNA of claim 1 , wherein the AS-siRNA is of 19-23 base pairs in length.

3. The AS-siRNA of claim 1 wherein the DNM2 gene is heterozygous for the presence of a disease-causing mutation.

4. The AS-siRNA of claim 3 , wherein said non-pathological polymorphism is on the same allele as the disease-causing mutation.

5. The AS-siRNA of claim 3 , wherein the disease-causing mutation is 1393C>T; c.1105C>T, c.1106G>A, c.1856C>T or c.1948G>A.

6. The AS-siRNA of claim 1 , wherein the AS-siRNA is of 19 base pairs in length and wherein the position of the sequence mismatch is located at position N16 or N17 from the 5′ end of the sense strand of said AS-siRNA.

7. The AS-siRNA of claim 1 , wherein the AS-siRNA comprises a sense strand selected from the group consisting of : SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 and SEQ ID NO:4.

8. The AS-siRNA of claim 1 , wherein the AS-siRNA reduces expression of DNM2 mRNA and/or DNM2 protein by 20-60%.

9. A vector encoding the AS-siRNA according to claim 1 .

10. An isolated target cell, which is transfected or transduced with the vector according to claim 9 .

11. An in vitro method for silencing the expression of a mutated allele of a DNM2 gene without silencing the expression of the wild type allele of the DNM2 gene in a target cell, comprising introducing in said target cell an AS-siRNA according to claim 1 or a vector encoding the AS-siRNA.

12. A method for ameliorating a disease selected from autosomal dominant centronuclear myopathy, myotubular myopathy, and Duchenne muscular dystrophy, in a subject in need thereof, comprising

administering to the subject a therapeutic amount of the AS-siRNA of claim 1 , or a vector encoding the AS-siRNA, or a cell transfected or transduced with the vector.

13. An AS-siRNA that comprises a sense strand selected from the group consisting of : SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9 and SEQ ID NO:10.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2019
From: BITOUN, MARC; TROCHET, DELPHINE; PRUDHON, BERNARD
To: ASSOCIATION INSTITUT DE MYOLOGIE; INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); SORBONNE UNIVERSITE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
Reel/Frame 049378/0376 →
Priority Claims (1)
EP 16306575 · Nov 29, 2016 · regional
Continuity (1)
Related Publication 20190309305A1 · Oct 10, 2019
Cited By (1)
US 12,275,941