TY - JOUR
T1 - Mushroom body evolution demonstrates homology and divergence across Pancrustacea
AU - Strausfeld, Nicholas James
AU - Wolff, Gabriella Hanna
AU - Sayre, Marcel Ethan
N1 - Funding Information: The research described here is supported by the National Science Foundation under Grants No. 1754798 awarded to NJS and No. 1754610 to GHW, as well as the University of Arizona’s Center for Insect Science, and funding to NJS from the University of Arizona Regents’ Fund. Our gratitude is directed to Daniel Kalderon, Columbia University, New York, for supplying the DC0 and RII antibodies, as he has during the last decade and longer. We thank the staff of the University of Washington’s Friday Harbor Marine Laboratories, San Juan, for their hospitality and unfailing help in obtaining living specimens. We have much profited from illuminating exchanges with Joanna M Wolfe, Harvard University, Cambridge, MA, for her crucial advice on the use of geological time lines and for identifying a number of errors in our original assessments. Charles Derby, Georgia State University, provided helpful advice on penaeid life cycles and habits. We are indebted to Camilla Strausfeld for critically discussing versions of the final manuscript, suggesting many improvements and meticulously editing the text. Funding Information: The research described here is supported by the National Science Foundation under Grants No. 1754798 awarded to NJS and No. 1754610 to GHW, as well as the University of Arizona?s Center for Insect Science, and funding to NJS from the University of Arizona Regents? Fund. Our gratitude is directed to Daniel Kalderon, Columbia University, New York, for supplying the DC0 and RII antibodies, as he has during the last decade and longer. We thank the staff of the University of Washington?s Friday Harbor Marine Laboratories, San Juan, for their hospitality and unfailing help in obtaining living specimens. We have much profited from illuminating exchanges with Joanna M Wolfe, Harvard University, Cambridge, MA, for her crucial advice on the use of geological time lines and for identifying a number of errors in our original assessments. Charles Derby, Georgia State University, provided helpful advice on penaeid life cycles and habits. We are indebted to Camilla Strausfeld for critically discussing versions of the final manuscript, suggesting many improvements and meticulously editing the text. National Science Foundation 1754798 Nicholas James Strausfeld National Science Foundation 1754610 Gabriella Hanna Wolff The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. Publisher Copyright: © Strausfeld et al.
PY - 2020/3
Y1 - 2020/3
N2 - Descriptions of crustacean brains have focused mainly on three highly derived lineages of malacostracans: the reptantian infraorders represented by spiny lobsters, lobsters, and crayfish. Those descriptions advocate the view that dome- or cap-like neuropils, referred to as ‘hemiellipsoid bodies,' are the ground pattern organization of centers that are comparable to insect mushroom bodies in processing olfactory information. Here we challenge the doctrine that hemiellipsoid bodies are a derived trait of crustaceans, whereas mushroom bodies are a derived trait of hexapods. We demonstrate that mushroom bodies typify lineages that arose before Reptantia and exist in Reptantia thereby indicating that the mushroom body, not the hemiellipsoid body, provides the ground pattern for both crustaceans and hexapods. We show that evolved variations of the mushroom body ground pattern are, in some lineages, defined by extreme diminution or loss and, in others, by the incorporation of mushroom body circuits into lobeless centers. Such transformations are ascribed to modifications of the columnar organization of mushroom body lobes that, as shown in Drosophila and other hexapods, contain networks essential for learning and memory.
AB - Descriptions of crustacean brains have focused mainly on three highly derived lineages of malacostracans: the reptantian infraorders represented by spiny lobsters, lobsters, and crayfish. Those descriptions advocate the view that dome- or cap-like neuropils, referred to as ‘hemiellipsoid bodies,' are the ground pattern organization of centers that are comparable to insect mushroom bodies in processing olfactory information. Here we challenge the doctrine that hemiellipsoid bodies are a derived trait of crustaceans, whereas mushroom bodies are a derived trait of hexapods. We demonstrate that mushroom bodies typify lineages that arose before Reptantia and exist in Reptantia thereby indicating that the mushroom body, not the hemiellipsoid body, provides the ground pattern for both crustaceans and hexapods. We show that evolved variations of the mushroom body ground pattern are, in some lineages, defined by extreme diminution or loss and, in others, by the incorporation of mushroom body circuits into lobeless centers. Such transformations are ascribed to modifications of the columnar organization of mushroom body lobes that, as shown in Drosophila and other hexapods, contain networks essential for learning and memory.
UR - http://www.scopus.com/inward/record.url?scp=85080980937&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85080980937&partnerID=8YFLogxK
U2 - 10.7554/eLife.52411
DO - 10.7554/eLife.52411
M3 - Article
C2 - 32124731
SN - 2050-084X
VL - 9
JO - eLife
JF - eLife
M1 - e52411
ER -