Optimal Decoding of Cellular Identities in a Genetic Network

Autor: Eric Wieschaus, William Bialek, Thomas Gregor, Mariela D. Petkova, Gašper Tkačik
Přispěvatelé: Harvard University, Department of Physics, Princeton University (DPPU), Princeton University, Institute of Science and Technology [Klosterneuburg, Austria] (IST Austria), Physique des fonctions biologiques / Physics of Biological Functions, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), This work was supported, in part, by U.S. NIH grants (P50GM071508, R01GM077599, and R01GM097275), U.S. NSF grants (PHY-1607612, CCF-0939370, Center for the Science of Information, PHY–1734030, Center for the Physics of Biological Function), an Austrian Science Fund grant (FWF P28844 to G.T.), and an Howard Hughes Medical Institute International Student Research Fellowship (to M.D.P.)., Harvard University [Cambridge], Institute of Science and Technology [Austria] (IST Austria), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Embryo
Nonmammalian

MESH: GTPase-Activating Proteins
0302 clinical medicine
MESH: Gene Expression Regulation
Developmental

Drosophila Proteins
MESH: Embryonic Development
Gene Regulatory Networks
MESH: Animals
MESH: Models
Genetic

[SDV.BDD]Life Sciences [q-bio]/Development Biology
MESH: Gene Regulatory Networks
0303 health sciences
cell fate
GTPase-Activating Proteins
Gene Expression Regulation
Developmental

Cell Differentiation
MESH: Transcription Factors
[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]
Drosophila melanogaster
Drosophila
developmental precision
Algorithm
Decoding methods
MESH: Body Patterning
MESH: Cell Differentiation
MESH: Drosophila Proteins
[PHYS.PHYS.PHYS-BIO-PH]Physics [physics]/Physics [physics]/Biological Physics [physics.bio-ph]
Genetic network
Embryonic Development
Cell fate determination
Biology
General Biochemistry
Genetics and Molecular Biology

Article
MESH: Drosophila melanogaster
03 medical and health sciences
Position (vector)
genetic networks
Animals
Enhancer
Gap gene
030304 developmental biology
Body Patterning
Models
Genetic

embryonic patterning
fungi
MESH: Embryo
Nonmammalian

cell specification
Expression (mathematics)
optimality
quantitative imaging
030217 neurology & neurosurgery
Free parameter
Transcription Factors
Zdroj: Cell
Cell, 2019, 176 (4), pp.844-855.e15. ⟨10.1016/j.cell.2019.01.007⟩
Cell, Elsevier, 2019, 176 (4), pp.844-855.e15. ⟨10.1016/j.cell.2019.01.007⟩
ISSN: 0092-8674
1097-4172
Popis: In developing organisms, spatially prescribed cell identities are thought to be determined by the expression levels of multiple genes. Quantitative tests of this idea, however, require a theoretical framework capable of exposing the rules and precision of cell specification over developmental time. Using the gap gene network in the early fly embryo as an example, we use such a framework to show how expression levels of the four gap genes can be jointly decoded into an optimal specification of position with 1% accuracy. The decoder correctly predicts, with no free parameters, the dynamics of pair-rule expression patterns at different developmental time points and in various mutant backgrounds. Precise cellular identities are thus available at the earliest stages of development, contrasting the prevailing view of positional information being slowly refined across successive layers of the patterning network. Our results suggest that developmental enhancers closely approximate a mathematically optimal decoding strategy.
Databáze: OpenAIRE