Search bioRxiv⌕ Search

bioRxiv · 10.1101/238279

Lhx2 regulates temporal changes in chromatin accessibility and transcription factor binding in retinal progenitor cells.

Abstract

Retinal progenitor cells (RPCs) pass through multiple stages of developmental competence, where they successively acquire and lose the ability to generate individual cell subtypes. To identify the transcriptional regulatory networks that control these transitions, we conducted epigenomic and transcriptomic profiling of early and late-stage RPCs and observed a developmentally dynamic landscape of chromatin accessibility. Open chromatin regions that showed stage-specificity, as well as those shared by early and late-stage RPCs, were selectively targeted by the homeodomain factor Lhx2, which is expressed throughout retinal neurogenesis but also regulates many stage-specific processes in RPCs. Stage-specific Lhx2 binding sites were frequently associated with target sites for transcription factors that are preferentially expressed in either early or late-stage RPCs, and which were predicted to possess pioneer activity. Lhx2 loss of function in RPCs led to a loss of chromatin accessibility at both direct Lhx2 target sites and more broadly across the genome, as well as a loss of binding by transcription factors associated with stage-specific Lhx2 target sites. These findings demonstrate a central role for Lhx2 in control of chromatin accessibility in RPCs, and identify transcription factors that may guide stage-specific target site selection by Lhx2.\n\nSummaryLhx2 is a central regulator of chromatin accessibility in retinal progenitor cells, and interacts with stage-specific transcription factors to regulate genes that are dynamically expressed during retinal neurogenesis.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Blackshaw, S., Zibetti, C., Liu, S., Wan, J., Qian, J.. 2017-12-21. Lhx2 regulates temporal changes in chromatin accessibility and transcription factor binding in retinal progenitor cells.. https://doi.org/10.1101/238279

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Expertise modifies neural responses to causal inference during language comprehension

Linguistic communication relies on shared common ground, yet different individuals in a community have specialized semantic knowledge. As a key example, physicians acquire rich knowledge about the causes of illness. An open question is whether such "causal expertise" influences the neural basis of language comprehension. Here we tested the hypothesis that when understanding everyday language like, "Holly used a grimy faucet during her overseas plane ride. Now she has the stomach flu," medical experts retrieve richer representations in semantic networks of the brain. Physicians (n=16) and age- and education-matched controls (n=16) undergoing fMRI read two-sentence vignettes that elicited implicit causal inferences about illness or object mechanics as well as control vignettes that did not elicit causal inferences. Vignettes were linguistically matched across conditions and were accessible to experts and non-experts alike. Across both groups, causal vignettes about illness engaged a temporoparietal semantic network previously implicated in thinking about animates, i.e., people and animals (precuneus and left temporoparietal junction), whereas causal vignettes about object mechanics engaged a semantic network associated with places and objects. Critically, physicians' responses in the animacy network were more robust and self-similar, suggesting the activation of richer semantic knowledge. Medical expertise effects were specific to biological inferences rather than mechanical or mental state inferences. By contrast, individually localized frontotemporal language and frontoparietal reasoning networks did not respond preferentially to causally connected sentences or show effects of expertise. Our findings suggest that causal expertise alters neural responses to causal inferences that unfold automatically during language comprehension.

neuroscience↗

The ViRA-L (Visual Recognition Assessment-Leuven): Development, Validation, and Age Stratified Normative Characterization of a Multi-Category Visual Recognition Battery

Objective: To develop and validate the Visual Recognition Assessment-Leuven (ViRA-L), a recognition-memory battery assessing ten visual categories within a matched task structure, and provide age-stratified normative data. Method: Healthy Dutch-speaking adults completed a visual recognition task for ten categories. Each category included six targets, 18 Learning trials, and 30 Novel trials requiring recognition across appearance changes. After exclusions, 417 participants remained. We evaluated reliability, score distributions, task effects, demographic associations, and category-specific norms. Results: Battery-level internal consistency was good (Cronbach's = .879; omega total = .901), with lower category-level estimates, broad score dispersion, and minimal floor and ceiling effects. Novel and difficult trials produced lower accuracy and slower responses. Age was the clearest demographic correlate of accuracy; gender and education showed no independent overall associations. Age effects varied by category and were larger in Novel than Learning trials. Model-based differences between ages 50 and 85 were largest for Pseudowords and Hands and smallest for Houses. Conclusions: The ViRA-L supports comparison of recognition-memory profiles under matched procedures. Category-dependent age associations support age-sensitive, category-specific interpretation. The battery provides a foundation for neuropsychological research; further validation is required for clinical diagnostic use.

neuroscience↗

Molecular MRI of Neuroinflammation in Alzheimer's Disease using a Folate-targeted Nanoprobe

Background: Neuroinflammation, driven by activated microglia, plays a central role in the pathogenesis of Alzheimer's disease (AD). Non-invasive imaging of neuroinflammation holds promise for advancing our understanding of disease mechanisms and evaluating anti-inflammatory therapeutic strategies. The folate receptor (FR), specifically its {beta} isoform, has been identified as a marker of pro-inflammatory myeloid cells in peripheral inflammatory diseases; however, its association with AD neuroinflammation remains unknown. In this work, we first determined FR expression in microglia in mouse models of AD and subsequently evaluated molecular MRI (mMRI) using a folate-targeted nanoprobe for in vivo imaging of the folate receptor expression. Methods and results: Microglial activation and FR expression in APP/PS1 and P301S transgenic mouse models of AD was measured using flow cytometry. A FR-targeted nanoprobe for mMRI was prepared by functionalizing high T1-relaxivity liposomal gadolinium nanoparticle with folic acid. Following intravenous injection, localization of the nanoprobe in the brains of aged transgenic and wild-type mice was measured using T1-weighted MRI. Post-mortem microscopy measured nanoprobe localization relative to microglia and amyloid pathology. In both mouse models, FR{beta} was significantly (p < 0.05) upregulated in pro-inflammatory microglia expressing TNF and IL-1{beta}. The folate-targeted nanoprobe demonstrated MR signal enhancement in the cortical and hippocampal regions of transgenic mice but not in wild type mice; non-targeted nanoprobe control did not demonstrate signal enhancement in brain of transgenic mice. Microscopy confirmed colocalization of FR-targeted nanoprobe with IBA1-positive microglia/macrophages and amyloid plaques. Conclusions: Pro-inflammatory microglia exhibit elevated levels of FR, and its measurement by non-invasive mMRI is a promising marker of neuroinflammation in AD.

neuroscience↗