Affiliation:
1. Department of Cell and Developmental Biology University of California San Diego La Jolla California USA
2. LOEWE Centre for Translational Biodiversity Genomics Frankfurt Germany
3. Senckenberg Research Institute Frankfurt Germany
4. Faculty of Biosciences Goethe University Frankfurt Frankfurt Germany
Abstract
AbstractVertebrate animals that run or jump across sparsely vegetated habitats, such as horses and jerboas, have reduced the number of distal limb bones, and many have lost most or all distal limb muscle. We previously showed that nascent muscles are present in the jerboa hindfoot at birth and that these myofibers are rapidly and completely lost soon after by a process that shares features with pathological skeletal muscle atrophy. Here, we apply an intra‐ and interspecies differential RNA‐Seq approach, comparing jerboa and mouse muscles, to identify gene expression differences associated with the initiation and progression of jerboa hindfoot muscle loss. We show evidence for reduced hepatocyte growth factor and fibroblast growth factor signaling and an imbalance in nitric oxide signaling; all are pathways that are necessary for skeletal muscle development and regeneration. We also find evidence for phagosome formation, which hints at how myofibers may be removed by autophagy or by nonprofessional phagocytes without evidence for cell death or immune cell activation. Last, we show significant overlap between genes associated with jerboa hindfoot muscle loss and genes that are differentially expressed in a variety of human muscle pathologies and rodent models of muscle loss disorders. All together, these data provide molecular insight into the process of evolutionary and developmental muscle loss in jerboa hindfeet.
Funder
National Institute of Arthritis and Musculoskeletal and Skin Diseases
National Institute of General Medical Sciences