Researchers find a small protein that plays a big role in heart muscle contraction January 22, 2016, 10:09

Significantly, the findings published today in Science offer a potential new target for developing therapeutics to boost the strength of cardiac muscle contractions in patients with heart failure, a chronic condition in which the heart pumps too weakly to supply adequate oxygen to the body.

The new protein, which the researchers have named dwarf open reading frame (DWORF), comprises just 34 amino acids, making it the third smallest protein known to be encoded in the mouse genome. By comparison, an average-sized protein is 10 times larger, including about 350 amino acids. DWORF is also encoded in the human genome.

The DWORF protein stimulates a calcium-ion pump that controls muscle contraction. As DWORF increases, the heart pumps with more force.

«There’s a brake in the heart that controls pumping, and DWORF shuts off the brake, which has the effect of making heart muscle pump more vigorously," said senior author Dr. Eric Olson, Chairman of the Molecular Biology, and Director of the Hamon Center for Regenerative Science and Medicine at UT Southwestern.

The researchers also found DWORF in some skeletal muscle, namely slow-twitch skeletal muscle fibers, the type of muscle fiber that allows a person to run marathons.

DWORF was found among a class of RNA transcripts that had been dismissed by scientists as non-coding RNA, sometimes colloquially called «junk» RNA. Emerging evidence, however, such as the discovery of DWORF, indicates that many small proteins with bioactive properties are hidden among these regions of the genome that are thought to be non-coding and, due to their small size, have evaded detection by scientists.

«Although small and non-enzymatic themselves, peptides like DWORF have the ability to regulate the function of much larger molecular complexes, analogous to the way that a tiny rudder determines the direction of a much larger ship," said Dr. Catherine Makarewich, a postdoctoral fellow in Dr. Olson’s lab and a co-lead author of the study.

«Elucidating the full catalog of small proteins like DWORF could provide significant new insight into how the molecular machinery of the cell is regulated," added Benjamin Nelson, a student in UT Southwestern’s Medical Scientist Training Program and co-lead author of the study.

«We dipped into the RNA ‘junk’ pile and came up with a hidden treasure," said Dr. Rhonda Bassel-Duby, Professor of Molecular Biology and a study author.

Other UT Southwestern researchers who contributed to the study are Dr. Douglas Anderson, postdoctoral fellow in Molecular Biology; Dr. Benjamin Winders, cardiology fellow; Austin Reese, graduate student researcher in Neuroscience; John McAnally, research scientist in Molecular Biology; and Dr. Ege Kavalali, Professor of Neuroscience and Physiology.

Dr. Kavalali holds the Rosewood Corporation Chair in Biomedical Science and is an Effie Cain Scholar in Medical Research. Dr. Olson holds the Annie and Willie Nelson Professorship in Stem Cell Research, the Pogue Distinguished Chair in Research on Cardiac Birth Defects, and the Robert A. Welch Distinguished Chair in Science.

This work was supported by grants from the National Institutes of Health, Foundation Leducq Networks of Excellence, the Cancer Prevention and Research Institute of Texas, the National Institute of Arthritis and Musculoskeletal Diseases, a Ruth L. Kirschstein National Research Service Award, and the Robert A. Welch Foundation