Dynamics of BMP signaling and stable gene expression in the early Drosophila embryo

Author:

Al Asafen Hadel1ORCID,Beseli Aydin1ORCID,Chen Hung-Yuan2ORCID,Hiremath Sharva34ORCID,Williams Cranos M.34ORCID,Reeves Gregory T.25ORCID

Affiliation:

1. North Carolina State University 1 Department of Chemical and Biomolecular Engineering , , Raleigh, NC 27695 , USA

2. Texas A&M University 2 Department of Chemical Engineering , , College Station, TX 77843, USA

3. North Carolina State University 3 Department of Electrical and Computer Engineering , , Raleigh, NC 27695, USA

4. North Carolina Plant Sciences Initiative, North Carolina State University 4 , Raleigh, NC 27695, USA

5. Interdisciplinary Graduate Program in Genetics, Texas A&M University 5 , College Station, TX 77843, USA

Abstract

ABSTRACT In developing tissues, morphogen gradients are thought to initialize gene expression patterns. However, the relationship between the dynamics of morphogen-encoded signals and gene expression decisions is largely unknown. Here we examine the dynamics of the Bone Morphogenetic Protein (BMP) pathway in Drosophila blastoderm-stage embryos. In this tissue, the BMP pathway is highly dynamic: it begins as a broad and weak signal on the dorsal half of the embryo, then 20-30 min later refines into a narrow, intense peak centered on the dorsal midline. This dynamical progression of the BMP signal raises questions of how it stably activates target genes. Therefore, we performed live imaging of the BMP signal and found that dorsal-lateral cells experience only a short transient in BMP signaling, after which the signal is lost completely. Moreover, we measured the transcriptional response of the BMP target gene pannier in live embryos and found it to remain activated in dorsal-lateral cells, even after the BMP signal is lost. Our findings may suggest that the BMP pathway activates a memory, or ‘ratchet’ mechanism that may sustain gene expression.

Funder

Texas A&M University

Publisher

The Company of Biologists

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