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Biology subjects

Pankaew, S.

Publications and source records attributed to Pankaew, S..

2 recordsLinked to original sources

AstroLogics: A simulation-based analysis framework for monotonous Boolean model ensemble

Boolean networks (BNs) have emerged as versatile tools for modeling cellular regulatory mechanisms due to their ability to capture key biological features despite their simplicity. Multiple BN synthesis methods, which aim to infer BNs with dynamics that corresponding to the experimental data, have emerged in a recent decade. However, these methods often posed a challenge as multiple BN candidates or "model ensemble" can be generated. While these ensembles are valuable for representing cell populations and their heterogeneity, current methods typically treat them as single components without examining their constituent features. We present AstroLogics, a novel framework designed to analyze and identify differences in both dynamical behavior and logical regulation within BN model ensembles. The framework calculates dynamical distances between BNs through exploration of their state transition graphs (STGs), enabling clustering of similarly functioning models that may represent different cellular fates or signaling mechanisms. AstroLogics also identifies key logical properties that govern each cluster, highlighting the core regulatory structures that differentiate model behaviors. Our approach leverages MaBoSS, a stochastic simulation tool that implements the Boolean Kinetic Monte-Carlo algorithm to address time interpretation in BNs. This probabilistic approximation method allows efficient probing of BN dynamics through stochastic simulations, overcoming the computational limitations of exhaustive STG analysis. Our framework also provides powerful visualization and classification capabilities for model ensembles. Through multiple use cases, we demonstrate how AstroLogics facilitates comprehensive analysis of model diversity, and discovery of key regulatory structures within BN ensembles.

bioinformatics↗

Single-cell transcriptome reveals a testis-specific expression profile of TCEA in human spermatogenesis

Transcription elongation factor A (TCEA) is a eukaryotic transcriptional molecule, required for a formation of initiation and elongation of gene transcription-mediated RNA polymerase II (RNAPII) complex, to promote transcription-coupled nucleotide excision repair (TC-NER) after RNAPII backtracking recovery. TCEA shares three isoforms in which TCEA1 is ubiquitously expressed among all eukaryotic cells. We found a spermatogenesis TCEA1 and TCEA2 expression profile has a unique transcriptional programme, compared with embryogenesis. Moreover, the testis-specific TCEA2 profile correlates with gene transcription, whereas TCEA1 specifically correlates with genes transcribed for Nuclear excision repair (NER) during human spermatogenesis. We also found that the expression activation of RNF20, a TCEA1 inhibitor, leads to expressional TCEA1 reduction, but having no direct impact on TCEA2 expression, implying the potential RNF20-dependent transcriptional switching of TCEA2 in transcriptional regulation during spermatogenesis. Our analysis defined a transcriptional bursting event where transcription-coupled repair (both Base excision repair and Nuclear excision repair) is a major pathway highly expressed in early spermatogenesis, supporting the transcriptional scanning hypothesis of which mutation of transcribed genes is effectively repaired as proposed by Xia B., et al. (2020).

bioinformatics↗