8.A.199. The Sarcolamban (Sarcolamban) Family
Short peptides (sarcolambans) of less than 30 amino acids regulate calcium transport via SARCA, and hence, they influence muscle contraction in the Drosophila heart. These peptides seem conserved for more than 550 million years in a range of species from flies to humans, in which they have been implicated in cardiac pathologies (Magny et al. 2013). Sarcolamban peptides are superinhibitors of mammalian SERCA, exhibiting either phospholamban-like or sarcolipin-like characteristics (Bak et al. 2022). The Drosophila endopeptidase Neprilysin 4 hydrolyzes SERCA-inhibitory sarcolamban peptides in membranes of the sarcoplasmic reticulum, thereby ensuring proper regulation of SERCA. Cleavage is necessary and sufficient to maintain homeostasis and function of the micropeptides. Analyses on human Neprilysin, sarcolipin, and ventricular cardiomyocytes indicates that the regulatory mechanism is evolutionarily conserved (Schiemann et al. 2022).
References:
Sarcolamban A of 28 aas and 1 TMS. See family description for functions.
Sarcolamban A of Drosophila melanogaster
Sarcolamban B of 29 aas and 1 TMSs. Inhibitor of the SERCA Ca2+-ATPase. See family description for functions.
Sarcolamban B of Drosophila melanogaster
Sarcolamban homolog of 28 aas and 1 TMS.
SclA homolog of Drosophila immigrans
Uncharacterized protein of 53 aas and 1 TMS. It shows 21% identity with sarcolamban B.
UP of Murimonas intestini