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Alejandro Colman-Lerner

Publications and source records attributed to Alejandro Colman-Lerner.

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Qualitatively Distinct Signaling in Cells: The Informational Landscape of Amplitude and Frequency Encoding

Cells continuously sense their surroundings to detect modifications and generate responses. Very often changes in extracellular concentrations initiate signaling cascades that eventually result in changes in gene expression. Increasing stimulus strengths can be encoded in increasing concentration amplitudes or increasing activation frequencies of intermediaries of the pathway. In this paper we show that the different way in which amplitude and frequency encoding map environmental changes endow cells with qualitatively different information transmission capabilities. While amplitude encoding is optimal for a limited range of stimuli strengths, frequency encoding can transmit information with equal reliability over much broader ranges. The qualitative difference between the two strategies stems from the scale invariant discriminating power of the first transducing step in frequency codification. The apparently redundant combination of both strategies in some cell types may then serve the purpose of expanding the span over which stimulus strengths can be reliably discriminated. In this paper we discuss a possible example of this mechanism in yeast.

q-bio.CB

Ultrasensitivity on signaling cascades revisited: Linking local and global ultrasensitivity estimations

Ultrasensitive response motifs, which are capable of converting graded stimulus in binary responses, are very well-conserved in signal transduction networks. Although it has been shown that a cascade arrangement of multiple ultrasensitive modules can produce an enhancement of the system's ultrasensitivity, how the combination of layers affects the cascade's ultrasensitivity remains an open question for the general case. Here we introduced a methodology that allowed us to determine the presence of sequestration effects and to quantify the relative contribution of each module to the overall cascade's ultrasensitivity. The proposed analysis framework provides a natural link between global and local ultrasensitivity descriptors and is particularly well-suited to characterize and better understand mathematical models used to study real biological systems. As a case study we considered three mathematical models introduced by O'Shaughnessy et al. to study a tunable synthetic MAPK cascade, and showed how our methodology might help modelers to better understand modeling alternatives.

q-bio.MN