RTL1 gene a likely culprit behind temple and Kagami-Ogata syndromes

RTL1 gene a likely culprit behind temple and Kagami-Ogata syndromes
HE staining in the neonatal intercostal muscle isolated from the mouse with Rtl1 overexpression after fixation (top) and its higher magnification views (bottom). Although the muscle fibers became larger than wild type, after fixation treatment they exhibited severe shrinkage (bottom). Credit: Department of Epigenetics,TMDU

Temple and Kagami-Ogata syndromes are serious genetic conditions that can lead to a variety of health problems with neonatal lethality, and in the case of Temple syndrome, severe growth problems occur. However, the genetic mechanisms of these illnesses are not well understood. But now, researchers from Tokyo Medical and Dental University (TMDU) have identified a gene that appears to be responsible for symptoms of both conditions, with important implications for human evolutionary genetics.

In a study published last month in Development the research team has revealed that deficiency and overproduction of Retrotransposon Gag like 1 (Rtl1), which is a mouse ortholog of the human RTL1 gene, is significantly associated with muscle symptoms in models of Temple and Kagami-Ogata syndromes, respectively.

Temple and Kagami-Ogata syndromes are characterized by unique postnatal muscle-related symptoms and prenatal placental problems. Although Rtl1 has previously been found to be responsible for prenatal placental malformations in mouse models of these conditions, the causative gene for the muscle-related symptoms has not been identified. The researchers at Tokyo Medical and Dental University (TMDU) aimed to address this in their recent study.

"Although Rtl1 is essential for maintaining placental fetal capillaries," says lead author of the study, Moe Kitazawa, "Little is known about the role of Rtl1 in other forms of muscular abnormalities."

The researchers extensively examined the role of Rtl1 in fetal muscle development at both the cellular and tissue level. They used two previously generated mouse models, one with a loss of Rtl1 to model Temple syndrome, and one with an overproduction of Rtl1 to Kagami-Ogata syndrome.

RTL1 gene a likely culprit behind temple and Kagami-Ogata syndromes
Immunofluorecence staining of RTL1 protein in the neonatal forelimb muscles from the mouse with Rtl1 overexpression. Long axis (left) view and cross-sectional views (right) of the muscle fibers. Co-immunostaining with RTL1 (red; arrowheads) and DESMIN (green; arrows) demonstrates that the RTL1 protein exists around the Z-disc in the muscle fiber. DAPI (blue) indicates nucleus. Credit: Department of Epigenetics,TMDU

"Our data clearly demonstrate that RTL1 is of critical physiological significance," explains Fumitoshi Ishino, senior author. "In the mouse models of both Temple and Kagami-Ogata syndrome, we detected severe but distinct abnormalities in the neonatal muscles that are necessary for respiration, such as the intercostal, abdominal, and diaphragm muscles."

Particularly, the overproduction of Rtl1 in the of Kagami-Ogata syndrome led to respiratory problems and muscle damage, resulting in neonatal death and the loss of Rtl1 was a major cause of abnormal muscle tone, such as hypotonia, and likely to be associated with feeding difficulty/poor sucking function in Temple patients.

Thus, RTL1 appears to be the major gene responsible for muscle and placental defects in these two genetic conditions.

"This is the first demonstration that a form of RTL1 specific to eutherians (placental mammals) plays an important role in fetal and neonatal development," says Kitazawa.

"This work demonstrates that LTR retrotransposons, which are a specific type of mobile DNA from which RTL1 originated, have influenced a variety of eutherian-specific traits, including the skeletal muscles, placenta, and the brain. Thus, these findings have important implications for understanding the acquisition of throughout the process of eutherian evolution," say senior authors Kaneko-Ishino and Ishino.

Explore further

Generation of three-dimensional heart organoids

More information: Moe Kitazawa et al, Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes, Development (2020). DOI: 10.1242/dev.185918
Journal information: Development

Provided by Tokyo Medical and Dental University
Citation: RTL1 gene a likely culprit behind temple and Kagami-Ogata syndromes (2020, October 6) retrieved 30 July 2021 from https://medicalxpress.com/news/2020-10-rtl1-gene-culprit-temple-kagami-ogata.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Feedback to editors

User comments