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High-throughput discovery of novel developmental phenotypes

Authors :
Dickinson, Mary E.
Flenniken, Ann M.
Ji, Xiao
Teboul, Lydia
Wong, Michael D.
White, Jacqueline K.
Meehan, Terrence F.
Weninger, Wolfgang J.
Westerberg, Henrik
Adissu, Hibret
Baker, Candice N.
Bower, Lynette
Brown, James M.
Caddle, L. Brianna
Chiani, Francesco
Clary, Dave
Cleak, James
Daly, Mark J.
Denegre, James M.
Doe, Brendan
Dolan, Mary E.
Edie, Sarah M.
Fuchs, Helmut
Gailus-Durner, Valerie
Galli, Antonella
Gambadoro, Alessia
Gallegos, Juan
Guo, Shiying
Horner, Neil R.
Hsu, Chih-Wei
Johnson, Sara J.
Kalaga, Sowmya
Keith, Lance C.
Lanoue, Louise
Lawson, Thomas N.
Lek, Monkol
Mark, Manuel
Marschall, Susan
Mason, Jeremy
McElwee, Melissa L.
Newbigging, Susan
Nutter, Lauryl M. J.
Peterson, Kevin A.
Ramirez-Solis, Ramiro
Rowland, Douglas J.
Ryder, Edward
Samocha, Kaitlin E.
Seavitt, John R.
Selloum, Mohammed
Szoke-Kovacs, Zsombor
Tamura, Masaru
Trainor, Amanda G.
Tudose, Ilinca
Wakana, Shigeharu
Warren, Jonathan
Wendling, Olivia
West, David B.
Wong, Leeyean
Yoshiki, Atsushi
MacArthur, Daniel G.
Tocchini-Valentini, Glauco P.
Gao, Xiang
Flicek, Paul
Bradley, Allan
Skarnes, William C.
Justice, Monica J.
Parkinson, Helen E.
Moore, Mark
Wells, Sara
Braun, Robert E.
Svenson, Karen L.
de Angelis, Martin Hrabe
Herault, Yann
Mohun, Tim
Mallon, Ann-Marie
Henkelman, R. Mark
Brown, Steve D. M.
Adams, David J.
Lloyd, K. C. Kent
McKerlie, Colin
Beaudet, Arthur L.
Bućan, Maja
Murray, Stephen A.
Dickinson, Mary E.
Flenniken, Ann M.
Ji, Xiao
Teboul, Lydia
Wong, Michael D.
White, Jacqueline K.
Meehan, Terrence F.
Weninger, Wolfgang J.
Westerberg, Henrik
Adissu, Hibret
Baker, Candice N.
Bower, Lynette
Brown, James M.
Caddle, L. Brianna
Chiani, Francesco
Clary, Dave
Cleak, James
Daly, Mark J.
Denegre, James M.
Doe, Brendan
Dolan, Mary E.
Edie, Sarah M.
Fuchs, Helmut
Gailus-Durner, Valerie
Galli, Antonella
Gambadoro, Alessia
Gallegos, Juan
Guo, Shiying
Horner, Neil R.
Hsu, Chih-Wei
Johnson, Sara J.
Kalaga, Sowmya
Keith, Lance C.
Lanoue, Louise
Lawson, Thomas N.
Lek, Monkol
Mark, Manuel
Marschall, Susan
Mason, Jeremy
McElwee, Melissa L.
Newbigging, Susan
Nutter, Lauryl M. J.
Peterson, Kevin A.
Ramirez-Solis, Ramiro
Rowland, Douglas J.
Ryder, Edward
Samocha, Kaitlin E.
Seavitt, John R.
Selloum, Mohammed
Szoke-Kovacs, Zsombor
Tamura, Masaru
Trainor, Amanda G.
Tudose, Ilinca
Wakana, Shigeharu
Warren, Jonathan
Wendling, Olivia
West, David B.
Wong, Leeyean
Yoshiki, Atsushi
MacArthur, Daniel G.
Tocchini-Valentini, Glauco P.
Gao, Xiang
Flicek, Paul
Bradley, Allan
Skarnes, William C.
Justice, Monica J.
Parkinson, Helen E.
Moore, Mark
Wells, Sara
Braun, Robert E.
Svenson, Karen L.
de Angelis, Martin Hrabe
Herault, Yann
Mohun, Tim
Mallon, Ann-Marie
Henkelman, R. Mark
Brown, Steve D. M.
Adams, David J.
Lloyd, K. C. Kent
McKerlie, Colin
Beaudet, Arthur L.
Bućan, Maja
Murray, Stephen A.

Abstract

Approximately one-third of all mammalian genes are essential for life. Phenotypes resulting from knockouts of these genes in mice have provided tremendous insight into gene function and congenital disorders. As part of the International Mouse Phenotyping Consortium effort to generate and phenotypically characterize 5,000 knockout mouse lines, here we identify 410 lethal genes during the production of the first 1,751 unique gene knockouts. Using a standardized phenotyping platform that incorporates high-resolution 3D imaging, we identify phenotypes at multiple time points for previously uncharacterized genes and additional phenotypes for genes with previously reported mutant phenotypes. Unexpectedly, our analysis reveals that incomplete penetrance and variable expressivity are common even on a defined genetic background. In addition, we show that human disease genes are enriched for essential genes, thus providing a dataset that facilitates the prioritization and validation of mutations identified in clinical sequencing efforts.

Details

Database :
OAIster
Notes :
10.1038/nature19356
Publication Type :
Electronic Resource
Accession number :
edsoai.on1147254833
Document Type :
Electronic Resource