Structure and function analysis of Sam68 and <scp>hnRNP A1</scp> synergy in the exclusion of exon 7 from <scp> <i>SMN2</i> </scp> transcripts-Reference-Cited by-同舟云学术

Structure and function analysis of Sam68 and hnRNP A1 synergy in the exclusion of exon 7 from SMN2 transcripts

Published:2023-03-22 Issue:4 Volume:32 Page:
ISSN:0961-8368
Container-title:Protein Science
language:en
Short-container-title:Protein Science

Author:

Nadal Marta¹,Anton Rosa¹,Dorca‐Arévalo Jonatan¹,Estébanez‐Perpiñá Eva²^ORCID,Tizzano Eduardo F.³⁴,Fuentes‐Prior Pablo¹^ORCID

Affiliation:

1. Molecular Bases of Disease Biomedical Research Institute Sant Pau (IIB Sant Pau) Barcelona Spain

2. Structural Biology of Nuclear Receptors, Department of Biochemistry and Molecular Biomedicine, Faculty of Biology Institute of Biomedicine (IBUB) of the University of Barcelona (UB) Barcelona Spain

3. Medicine Genetics Group Vall d'Hebron Research Institute (VHIR) Barcelona Spain

4. Department of Clinical and Molecular Genetics Hospital Vall d'Hebron Barcelona Spain

Funder

The Daniel Bravo Andreu Private Foundation

Ministry of Science and Innovation

Spinal Muscular Atrophy Foundation

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pro.4553

Reference69 articles.

1. Solution structure of the two RNA recognition motifs of hnRNP A1 using segmental isotope labeling: how the relative orientation between RRMs influences the nucleic acid binding topology

2. Hypoxia is a modifier of SMN2 splicing and disease severity in a severe SMA mouse model

3. Antisense Oligonucleotide Therapies for Neurodegenerative Diseases

4. The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

5. Tandem hnRNP A1 RNA recognition motifs act in concert to repress the splicing of survival motor neuron exon 7

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