|Title||Paused Pol II coordinates tissue morphogenesis in the Drosophila embryo.|
|Publication Type||Journal Article|
|Year of Publication||2013|
|Authors||Lagha, M, Bothma, JP, Esposito, E, Ng, S, Stefanik, L, Tsui, C, Johnston, J, Chen, K, Gilmour, DS, Zeitlinger, J, Levine, MS|
|Date Published||2013 May 23|
|Keywords||Animals, Base Sequence, Drosophila melanogaster, Drosophila Proteins, Embryo, Nonmammalian, Gastrulation, Gene Expression Regulation, Developmental, Models, Biological, Molecular Sequence Data, Morphogenesis, Promoter Regions, Genetic, RNA Polymerase II, Transcription, Genetic|
Paused RNA polymerase (Pol II) is a pervasive feature of Drosophila embryos and mammalian stem cells, but its role in development is uncertain. Here, we demonstrate that a spectrum of paused Pol II determines the "time to synchrony"-the time required to achieve coordinated gene expression across the cells of a tissue. To determine whether synchronous patterns of gene activation are significant in development, we manipulated the timing of snail expression, which controls the coordinated invagination of ∼1,000 mesoderm cells during gastrulation. Replacement of the strongly paused snail promoter with moderately paused or nonpaused promoters causes stochastic activation of snail expression and increased variability of mesoderm invagination. Computational modeling of the dorsal-ventral patterning network recapitulates these variable and bistable gastrulation profiles and emphasizes the importance of timing of gene activation in development. We conclude that paused Pol II and transcriptional synchrony are essential for coordinating cell behavior during morphogenesis.