Pre-steady-state decoding of the Bicoid morphogen gradient.

Abstract:

:Morphogen gradients are established by the localized production and subsequent diffusion of signaling molecules. It is generally assumed that cell fates are induced only after morphogen profiles have reached their steady state. Yet, patterning processes during early development occur rapidly, and tissue patterning may precede the convergence of the gradient to its steady state. Here we consider the implications of pre-steady-state decoding of the Bicoid morphogen gradient for patterning of the anterior-posterior axis of the Drosophila embryo. Quantitative analysis of the shift in the expression domains of several Bicoid targets (gap genes) upon alteration of bcd dosage, as well as a temporal analysis of a reporter for Bicoid activity, suggest that a transient decoding mechanism is employed in this setting. We show that decoding the pre-steady-state morphogen profile can reduce patterning errors caused by fluctuations in the rate of morphogen production. This can explain the surprisingly small shifts in gap and pair-rule gene expression domains observed in response to alterations in bcd dosage.

journal_name

PLoS Biol

journal_title

PLoS biology

authors

Bergmann S,Sandler O,Sberro H,Shnider S,Schejter E,Shilo BZ,Barkai N

doi

10.1371/journal.pbio.0050046

subject

Has Abstract

pub_date

2007-02-01 00:00:00

pages

e46

issue

2

eissn

1544-9173

issn

1545-7885

pii

06-PLBI-RA-1783R2

journal_volume

5

pub_type

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