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Guerrero, L. A.

Publications and source records attributed to Guerrero, L. A..

3 recordsLinked to original sources

Chromatin accessibility and heat stress gene expression in the reef-building coral, Acropora millepora

Understanding how organisms regulate gene expression to maintain homeostasis in the face of environmental changes is critical, particularly considering increasing climate stressors. While DNA methylation has dominated the literature on epigenetic control of gene expression in ecological systems, alternative epigenetic layers may provide additional insight into mechanisms of gene expression regulation. This study investigates the role of chromatin accessibility in influencing gene expression in the reef-building coral Acropora millepora, especially in response to thermal stress. We find that highly accessible regions of chromatin, or open chromatin, are predominantly located in distal intergenic regions, promoters, and introns. Genes with open promoters exhibit increased expression and reduced variability, suggesting that chromatin accessibility may influence gene expression plasticity. The baseline state of promoter accessibility is weakly correlated with the expression response to heat stress, suggesting chromatin state can influence organismal response to environmental stress. This study contributes new insights into regulatory mechanisms important for responding to acute environmental stressors. This work also establishes a foundation to investigate the interactions between chromatin accessibility, additional epigenetic layers, and how the dynamics of these interacting epigenetic layers contribute to adaptive molecular and cellular responses, which will be critical for understanding organismal resilience to ongoing environmental change.

genomics↗

A CDC-42-regulated actin network is necessary for nuclear migration through constricted spaces in C. elegans

Successful nuclear migration through constricted spaces between cells or in the extracellular matrix relies on the ability of the nucleus to deform. Little is known of how this takes place in vivo. We study confined nuclear migration in Caenorhabditis elegans larval P-cells, which is mediated by the LINC complex to pull nuclei towards the minus ends of microtubules. Null mutations of LINC component unc-84 lead to a temperature-dependent phenotype, suggesting a parallel pathway for P-cell nuclear migration. A forward genetic screen for enhancers of unc-84 identified cgef-1 (CDC-42 Guanine Nucleotide Exchange Factor). Knockdown of CDC-42 in the absence of the LINC complex led to a P-cell nuclear migration defect. Expression of constitutively active CDC-42 rescued nuclear migration in cgef-1; unc-84 double mutants suggesting CDC-42 functions downstream of CGEF-1. The Arp2/3 complex and non-muscle myosin II (NMY-2) were also found to function parallel to the LINC pathway. In our model, CGEF-1 activates CDC-42, induces actin polymerization through the Arp2/3 complex to deform the nucleus during nuclear migration while NMY-2 helps push the nucleus through confined spaces.

developmental biology↗

The Nesprin-1/-2 ortholog ANC-1 regulates organelle positioning in C. elegans without its KASH or actin-binding domains

KASH proteins in the outer nuclear membrane comprise the cytoplasmic half of LINC complexes that connect nuclei to the cytoskeleton. Caenorhabditis elegans ANC-1, an ortholog of Nesprin-1/2, contains actin-binding and KASH domains at opposite ends of a long spectrin-like region. Deletion of either the KASH or calponin homology (CH) domains does not completely disrupt nuclear positioning, suggesting neither KASH nor CH domains are essential. Deletions in the spectrin-like region of ANC-1 led to significant defects, but only recapitulated the null phenotype in combination with mutations in the trans-membrane span. In anc-1 mutants, the ER was unanchored, moving throughout the cytoplasm, and often fragmented. The data presented here support a cytoplasmic integrity model where ANC-1 localizes to the ER membrane and extends into the cytoplasm to position nuclei, ER, mitochondria, and likely other organelles in place.

cell biology↗