TY - JOUR
T1 - Three-dimensional flagella structures from animals’ closest unicellular relatives, the Choanoflagellates
AU - Pinskey, Justine M.
AU - Lagisetty, Adhya
AU - Gui, Long
AU - Phan, Nhan
AU - Reetz, Evan
AU - Tavakoli, Amirrasoul
AU - Fu, Gang
AU - Nicastro, Daniela
N1 - Funding Information:
The authors acknowledge Drs. Julie Pfeiffer and Arielle Woznica (UT Southwestern Medical Center) for their generous assistance sharing reagents and knowledge of choanoflagellate cell culture, Drs. Jeffrey Woodruff and Maralice Connaci-Sorell (UT Southwestern Medical Center) for sharing equipment, reagents, and advice, and John Heumann and David Mastronarde (University of Colorado, Boulder) for technical advice concerning IMOD. We are also grateful to Dr. Daniel Stoddard, Jose Martinez, Raymond Welch, and Eric Zhang of the Cryo-EM Facility at UT Southwestern Medical Center, as well as current and previous Nicastro lab members, for their ongoing assistance and support. Cryo-EM data were collected at the UT Southwestern Medical Center Cryo-Electron Microscopy Facility, which is supported in part by the CPRIT Core Facility Support Award RP170644. This study was funded by the following grants: National Institutes of Health grants R01GM083122 (to DN) and F32 GM137470 (to JMP), and a Cancer Prevention and Research Institute of Texas (CPRIT) grant RR140082 (to DN). This research was also supported in part by the computational resources provided by the BioHPC supercomputing facility located in the Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center. Cryo-ET data for the 96 nm flagellar repeat average, central pair complex average, and barb average have been deposited to the EM Data Bank under accession codes EMD-26204, EMD-26209, and EMD-26210, respectively.
Funding Information:
The authors acknowledge Drs. Julie Pfeiffer and Arielle Woznica (UT Southwestern Medical Center) for their generous assistance sharing reagents and knowledge of choanoflagellate cell culture, Drs. Jeffrey Woodruff and Maralice Connaci-Sorell (UT Southwestern Medical Center) for sharing equipment, reagents, and advice, and John Heumann and David Mastronarde (University of Colorado, Boulder) for technical advice concerning IMOD. We are also grateful to Dr. Daniel Stoddard, Jose Martinez, Raymond Welch, and Eric Zhang of the Cryo-EM Facility at UT Southwestern Medical Center, as well as current and previous Nicastro lab members, for their ongoing assistance and support. Cryo-EM data were collected at the UT Southwestern Medical Center Cryo-Electron Microscopy Facility, which is supported in part by the CPRIT Core Facility Support Award RP170644. This study was funded by the following grants: National Institutes of Health grants R01GM083122 (to DN) and F32 GM137470 (to JMP), and a Cancer Prevention and Research Institute of Texas (CPRIT) grant RR140082 (to DN). This research was also supported in part by the computational resources provided by the BioHPC super-computing facility located in the Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center. Cryo-ET data for the 96 nm flagellar repeat average, central pair complex average, and barb average have been deposited to the EM Data Bank under accession codes EMD-26204, EMD-26209, and EMD-26210, respectively.Justine M Pinskey http://orcid.org/0000-0001-5656-5519Daniela Nicastro http://orcid.org/0000-0002-0122-7173.
Publisher Copyright:
© Pinskey et al.
PY - 2022/11
Y1 - 2022/11
N2 - In most eukaryotic organisms, cilia and flagella perform a variety of life-sustaining roles related to environmental sensing and motility. Cryo-electron microscopy has provided considerable insight into the morphology and function of flagellar structures, but studies have been limited to lesthan a dozen of the millions of known eukaryotic species. Ultrastructural information is particularly lacking for unicellular organisms in the Opisthokonta clade, leaving a sizeable gap in our under-standing of flagella evolution between unicellular species and multicellular metazoans (animals). Choanoflagellates are important aquatic heterotrophs, uniquely positioned within the opisthokonts as the metazoans’ closest living unicellular relatives. We performed cryo-focused ion beam milling and cryo-electron tomography on flagella from the choanoflagellate species Salpingoeca rosetta. Wshow that the axonemal dyneins, radial spokes, and central pair complex in S. rosetta more closely resemble metazoan structures than those of unicellular organisms from other suprakingdoms. In addition, we describe unique features of S. rosetta flagella, including microtubule holes, microtubule inner proteins, and the flagellar vane: a fine, net-like extension that has been notoriously difficult to visualize using other methods. Furthermore, we report barb-like structures of unknown function on the extracellular surface of the flagellar membrane. Together, our findings provide new insights into choanoflagellate biology and flagella evolution between unicellular and multicellular opisthokonts.
AB - In most eukaryotic organisms, cilia and flagella perform a variety of life-sustaining roles related to environmental sensing and motility. Cryo-electron microscopy has provided considerable insight into the morphology and function of flagellar structures, but studies have been limited to lesthan a dozen of the millions of known eukaryotic species. Ultrastructural information is particularly lacking for unicellular organisms in the Opisthokonta clade, leaving a sizeable gap in our under-standing of flagella evolution between unicellular species and multicellular metazoans (animals). Choanoflagellates are important aquatic heterotrophs, uniquely positioned within the opisthokonts as the metazoans’ closest living unicellular relatives. We performed cryo-focused ion beam milling and cryo-electron tomography on flagella from the choanoflagellate species Salpingoeca rosetta. Wshow that the axonemal dyneins, radial spokes, and central pair complex in S. rosetta more closely resemble metazoan structures than those of unicellular organisms from other suprakingdoms. In addition, we describe unique features of S. rosetta flagella, including microtubule holes, microtubule inner proteins, and the flagellar vane: a fine, net-like extension that has been notoriously difficult to visualize using other methods. Furthermore, we report barb-like structures of unknown function on the extracellular surface of the flagellar membrane. Together, our findings provide new insights into choanoflagellate biology and flagella evolution between unicellular and multicellular opisthokonts.
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U2 - 10.7554/eLife.78133
DO - 10.7554/eLife.78133
M3 - Article
C2 - 36384644
AN - SCOPUS:85142161108
SN - 2050-084X
VL - 11
JO - eLife
JF - eLife
M1 - e78133
ER -