TY - JOUR
T1 - Unde venisti PGRMC? Grand-scale biology from early Eukaryotes and Eumetazoan animal origins
AU - Cahill, Michael A.
N1 - Funding Information:
I am grateful to Tim Cahill (R.I.P.) for Latin language assistance.
Publisher Copyright:
© 2022 The Author(s). Published by IMR Press.
PY - 2022/11/30
Y1 - 2022/11/30
N2 - The title usage of Unde venisti ‘from where have you come’ is from a now dead language (Latin) that foundationally influenced modern English (not the major influence, but an essential formative one). This is an apt analogy for how both the ancient eukaryotic and eumetazoan functions of PGRMC proteins (PGRMC1 and PGRMC2 in mammals) probably influence modern human biology: via a formative trajectory from an evolutionarily foundational fulcrum. There is an arguable probability, although not a certainty, that PGRMC-like proteins were involved in eukaryogenesis. If so, then the proto-eukaryotic ancestral protein is modelled as having initiated the oxygen-induced and CYP450 (Cytochrome P450)-mediated synthesis of sterols in the endoplasmic reticulum to regulate proto-mitochondrial activity and heme homeostasis, as well as having enabled sterol transport between endoplasmic reticulum (ER) and mitochondria membranes involving the actin cytoskeleton, transport of heme from mitochondria, and possibly the regulation/origins of mitosis/meiosis. Later, during animal evolution, the last eumetazoan common ancestor (LEUMCA) acquired PGRMC phosphorylated tyrosines coincidentally with the gastrulation organizer, Netrin/deleted in colorectal carcinoma (DCC) signaling, muscle fibers, synapsed neurons, and neural recovery via a sleep-like process. Modern PGRMC proteins regulate multiple functions, including CYP450-mediated steroidogenesis, membrane trafficking, heme homeostasis, glycolysis/Warburg effect, fatty acid metabolism, mitochondrial regulation, and genomic CpG epigenetic regulation of gene expression. The latter imposes the system of differentiation status-sensitive cell-type specific proteomic complements in multi-tissued descendants of the LEUMCA. This paper attempts to trace PGRMC functions through time, proposing that key functions were involved in early eukaryotes, and were later added upon in the LEUMCA. An accompanying paper considers the implications of this awareness for human health and disease.
AB - The title usage of Unde venisti ‘from where have you come’ is from a now dead language (Latin) that foundationally influenced modern English (not the major influence, but an essential formative one). This is an apt analogy for how both the ancient eukaryotic and eumetazoan functions of PGRMC proteins (PGRMC1 and PGRMC2 in mammals) probably influence modern human biology: via a formative trajectory from an evolutionarily foundational fulcrum. There is an arguable probability, although not a certainty, that PGRMC-like proteins were involved in eukaryogenesis. If so, then the proto-eukaryotic ancestral protein is modelled as having initiated the oxygen-induced and CYP450 (Cytochrome P450)-mediated synthesis of sterols in the endoplasmic reticulum to regulate proto-mitochondrial activity and heme homeostasis, as well as having enabled sterol transport between endoplasmic reticulum (ER) and mitochondria membranes involving the actin cytoskeleton, transport of heme from mitochondria, and possibly the regulation/origins of mitosis/meiosis. Later, during animal evolution, the last eumetazoan common ancestor (LEUMCA) acquired PGRMC phosphorylated tyrosines coincidentally with the gastrulation organizer, Netrin/deleted in colorectal carcinoma (DCC) signaling, muscle fibers, synapsed neurons, and neural recovery via a sleep-like process. Modern PGRMC proteins regulate multiple functions, including CYP450-mediated steroidogenesis, membrane trafficking, heme homeostasis, glycolysis/Warburg effect, fatty acid metabolism, mitochondrial regulation, and genomic CpG epigenetic regulation of gene expression. The latter imposes the system of differentiation status-sensitive cell-type specific proteomic complements in multi-tissued descendants of the LEUMCA. This paper attempts to trace PGRMC functions through time, proposing that key functions were involved in early eukaryotes, and were later added upon in the LEUMCA. An accompanying paper considers the implications of this awareness for human health and disease.
KW - Steroid biology; eukaryogenesis; membrane-associated progesterone receptor; neurogenesis: neurobiology; synapse; cyP51A1; Candidate Phyla Radiation bacteria; heme; redox; metabolism; translational control; eumetazoa; eumetazoans; LEUMCA; gastrulation; gas
KW - membrane-associated progesterone receptor
KW - neurogenesis
KW - neurobiology
KW - synapse
KW - cyP51A1
KW - Candidate Phyla Radiation bacteria
KW - heme
KW - redox
KW - metabolism
KW - translational control
KW - eumetazoa
KW - eumetazoans
KW - LEUMCA
KW - gastrulation
KW - gastrulation organizer
KW - blastoporal axial organizer
KW - pluripotent stem cells
KW - TMEM97
KW - Sigma-2 Receptor
KW - cell motility
KW - sleep
KW - epigenetics
KW - aging
KW - aging clock
KW - tyrosine phosphorylation
KW - Epithelial-Mesenchymal Transition
KW - EMT
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U2 - 10.31083/j.fbl2711317
DO - 10.31083/j.fbl2711317
M3 - Review article
C2 - 36472108
SN - 2768-6698
VL - 27
SP - 317
JO - Frontiers in Bioscience - Landmark
JF - Frontiers in Bioscience - Landmark
IS - 11
M1 - 317
ER -