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Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene?

  • Anna GaertnerEmail author
  • Andreas Brodehl
  • Hendrik MiltingEmail author
Open Access
COMMENTARY
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With great interest we have read the study of Liu et al. (2018) revealing the role of RNA binding protein 24 (RBM24) on global alternative splicing and dilated cardiomyopathy (DCM) in mice. As suggested previously, deficiency of Rbm24 causes embryonic lethality limiting the functional analyses (Yang et al., 2014). To circumvent this limitation the authors generated cardiac specific Rbm24 deficient mice and showed that homozygous deletion of Rbm24 at postnatal stage leads to rapidly progressive DCM and heart failure (Liu et al., 2018).

DCM is considered as the most common type of cardiomyopathy (Fu and Eisen, 2018). It is estimated that about 60% of DCM cases have a genetic etiology (Klauke et al., 2017). However, the associated genotypes are highly diverse and mutations in at least 50 genes have been described with DCM (Stenson et al., 2003). These genes are encoding proteins of the sarcomere, the cytoskeleton, the nuclear envelope, components of the Ca2+ transient, ion channels and transcription (co)-factors. In addition, several regulators of alternative splicing like muscleblind like splicing regulator 1 (MBNL1) (LeMasters et al., 2012), RNA binding fox-1 homolog 1 (RBFOX1) (Gao et al., 2016), RNA binding fox-1 homolog 2 (RBFOX2) (Wei et al., 2015), RBM24 (Liu et al., 2018) might have impact on cardiac development and/or the cardiac function in animal models. However, the role of these proteins in human cardiomyopathy is still unknown. At present, only mutations in the gene RBM20 encoding a cardiac splice factor have been shown to be associated with cardiomyopathy (Brauch et al., 2009; Wells et al., 2013; Beqqali et al., 2016).

Conditional deletion of Rbm24 is associated with 590 altered splicing events in mice. The affected proteins are involved in cytoskeleton organization, striated muscle cell differentiation, heart contraction and cardiovascular development (Liu et al., 2018). Interestingly, the study of Liu et al. demonstrated convincingly that one of the direct splicing targets of murine Rbm24 is Ttn, coding for the giant sarcomeric protein titin. RNA binding protein 20 (RBM20) was the only known splicing factor of TTN (Guo et al., 2012). Remarkably, mutations in RBM20 are not so rare among DCM-patients and cause frequently a severe clinical phenotype (Brauch et al., 2009; Ma et al., 2016).

We think that the study of Liu et al. might has also relevance for human cardiovascular genetics because it can be suggested that RBM24 mutations might be involved in human cardiomyopathies, especially because no disease associated RBM24-mutations have been described until now.

Even if familial cardiomyopathy is suspected, the identification of the causative pathogenic gene mutation is not always possible. In consequence, the identification of novel cardiomyopathy associated genes remains a major issue of human cardiovascular genetics having clinical impact for genetic counselling of affected families.

As RBM24 was already established as a major regulator of muscle-specific alternative splicing (Yang et al., 2014) we analyzed the coding sequence of three RBM24-splice variants (NM_001143942, NM_153020, NM_001143941) in 190 cardiomyopathy index patients by Sanger sequencing. To our surprise, we did not find any pathogenic RBM24 mutation. Although we cannot exclude that in further specific cases pathogenic RBM24 mutations might be found, our data suggest that RBM24 mutations are rare in human cardiomyopathy patients. Thus, the data of our cohort suggests an allele frequency in non-ischemic cardiomyopathy patients below <0.5%. These findings are supported by the fact that only the homozygous Rbm24 deficient mice developed DCM in the study by Liu and colleagues (2018).

In summary, it remains an open question if RBM24 can be established as a rare cardiomyopathy associated gene. However, with relevance for clinical cardiovascular genetics this gene deserves further attention in genetic screenings.

Notes

COMPLIANCE WITH ETHICS GUIDELINES

Anna Gaertner, Andreas Brodehl and Hendrik Milting declare that they have no conflict of interest. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000. Informed consent was obtained from all patients for being included in the study.

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© The Author(s) 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Erich and Hanna Klessmann Institute, Heart and Diabetes Center NRWUniversity Hospital of the Ruhr-University BochumBad OeynhausenGermany

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