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Gleason, R. J.

Publications and source records attributed to Gleason, R. J..

3 recordsLinked to original sources

Modulating DNA Polα Enhances Cell Reprogramming Across Species

As a fundamental biological process, DNA replication ensures the accurate copying of genetic information. However, the impact of this process on cellular plasticity in multicellular organisms remains elusive. Here, we find that reducing the level or activity of a replication component, DNA Polymerase (Pol), facilitates cell reprogramming in diverse stem cell systems across species. In Drosophila male and female germline stem cell lineages, reducing Pol levels using heterozygotes significantly enhances fertility of both sexes, promoting reproductivity during aging without compromising their longevity. Consistently, in C. elegans the pola heterozygous hermaphrodites exhibit increased fertility without a reduction in lifespan, suggesting that this phenomenon is conserved. Moreover, in male germline and female intestinal stem cell lineages of Drosophila, pol heterozygotes exhibit increased resistance to tissue damage caused by genetic ablation or pathogen infection, leading to enhanced regeneration and improved survival during post-injury recovery, respectively. Additionally, fine tuning of an inhibitor to modulate Pol activity significantly enhances the efficiency of reprogramming human embryonic fibroblasts into induced pluripotent cells. Together, these findings unveil novel roles of a DNA replication component in regulating cellular reprogramming potential, and thus hold promise for promoting tissue health, facilitating post-injury rehabilitation, and enhancing healthspan.

developmental biology↗

Developmentally programmed epigenome regulates cellular plasticity at the parental-to-zygote transition

During metazoan development, the dramatic potency change from germline to embryos raises an important question regarding how the new life cycle is reset. Here, we report a tightly regulated epigenome landscape change from the parental germline to embryos in C. elegans. The epigenome is enriched with histone H3 in early-stage germ cells but switches to a histone variant H3.3-enriched epigenome in the mature egg. This H3.3-dominant epigenome persists in early-stage embryos until gastrulation, when the epigenome becomes H3 abundant again. We further demonstrate that this developmentally programmed H3 [->] H3.3 [->] H3 epigenome landscape change is regulated through differential expression of distinct histone gene clusters and is required for both germline integrity and early embryonic cellular plasticity. Together, this study reveals that a bimodal expression of H3 versus H3.3 is important for epigenetic reprogramming during gametogenesis and embryonic plasticity. One Sentence SummaryDevelopmentally programmed epigenome resets cellular plasticity at the parental-to-zygote transition in C. elegans.

developmental biology↗

C. elegans models of Marfan and Marfan-like Syndromes reveal trafficking defects of the type II TGFβ receptor as a potential novel disease mechanism

The transforming growth factor-{beta} (TGF{beta}) family plays an important role in many developmental processes and when mutated often contributes to various diseases. Marfan syndrome is a genetic disease with an occurrence of approximately 1 in 5,000. The disease is caused by mutations in fibrillin, which lead to an increase in TGF{beta} ligand activity, resulting in abnormalities of connective tissues which can be life-threatening. Mutations in other components of TGF{beta} signaling (receptors, Smads, Schnurri) lead to similar diseases with attenuated phenotypes relative to Marfan syndrome. In particular, mutations in TGF{beta} receptors, most of which are clustered at the C-terminal end, result in Marfan-like (MFS-like) syndromes. Even though it was assumed that many of these receptor mutations would reduce or eliminate signaling, in many cases signaling is active. From our trafficking work in C. elegans, we noticed that many of these receptor mutations that lead to Marfan-like syndromes overlap with mutations that cause mis-trafficking of the receptor, suggesting a link between Marfan-like syndromes and TGF{beta} receptor trafficking. To test this hypothesis, we introduced some of these key MFS and MFS-like mutations into the C. elegans TGF{beta} receptor and asked if receptor trafficking is altered. We find that some of the mutated receptors localize to the apical surface rather than basolateral surface of the polarized intestinal cells. Further, we find that these mutations result in longer animals, a phenotype due to over-stimulation of the pathway and, importantly, indicating that function of the receptor is not abrogated in these mutants. Our nematode models of Marfan syndrome suggest that MFS and MFS-like mutations in the type II receptor lead to mis-trafficking of the receptor and possibly provides an explanation for the disease, a phenomenon which might also occur in some cancers that possess the same mutations within the type II receptor (e.g. colon cancer). Author SummaryThe transforming growth factor-{beta} (TGF{beta}) family plays an important role in many basic biological processes and when mutated often contributes to various diseases. Marfan syndrome (MFS) is a genetic disease with an occurrence of approximately 1 in 5,000. The disease is caused by mutations in fibrillin, which lead to an increase in TGF{beta} ligand activity, resulting in abnormalities of connective tissues which can be life-threatening. However, some patients with normal fibrillin genes also show symptoms and pathologies associated with Marfan syndrome, known collectively as Marfan-like Syndromes (MFS-like). When these patients were assessed for mutations in other components of the TGF{beta} pathway, several mutations clustered in a small region of the receptors, primarily in the type II TGF{beta} receptor were found. We find that mimicking these mutations in the nematode type II TGF{beta} receptor causes the mutant receptor to move to regions of the cell where it is not normally found. Importantly, these mutations do not abrogate the function of the receptor, suggesting that mis-localization of the receptor might be previously unknown cause of disease etiology. We hypothesize that receptor mutations present at the LTA lead to disruptions in interactions with trafficking regulators leading to symptoms of MFS/MFS-like syndromes - a novel disease mechanism of MFS/MFS-like syndromes that might also extend to other cancers bearing similar mutations.

cancer biology↗