10 results on '"Mill, Jon"'
Search Results
2. A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy
- Author
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Brookes, Keeley-Joanne, Mill, Jon, Guindalini, Camilla, Curran, Sarah, Xu, Xiaohui, Knight, Jo, Chen, Chih-Ken, Huang, Yu-Shu, Sethna, Vaheshta, Taylor, Eric, Chen, Wai, Breen, Gerome, and Asherson, Philip
- Subjects
Attention-deficit hyperactivity disorder -- Genetic aspects ,Attention-deficit hyperactivity disorder -- Risk factors ,Haplotypes -- Analysis ,Dopamine -- Research ,Drinking in pregnancy -- Research ,Health ,Psychology and mental health - Published
- 2006
3. TRANSCRIPTOMIC STUDIES OF THE HUMAN PRENATAL BRAIN
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O'Brien, Heath, primary, Hannon, Eilis, additional, Spiers, Helen, additional, Jeffries, Aaron, additional, McLaughlin, Gemma, additional, Davies, William, additional, Anney, Richard, additional, Hill, Matthew, additional, O'Donovan, Michael, additional, Mill, Jon, additional, and Bray, Nick, additional
- Published
- 2019
- Full Text
- View/download PDF
4. 36 - TRANSCRIPTOMIC STUDIES OF THE HUMAN PRENATAL BRAIN
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O'Brien, Heath, Hannon, Eilis, Spiers, Helen, Jeffries, Aaron, McLaughlin, Gemma, Davies, William, Anney, Richard, Hill, Matthew, O'Donovan, Michael, Mill, Jon, and Bray, Nick
- Published
- 2019
- Full Text
- View/download PDF
5. Guns for America
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Mill, Jon
- Subjects
Hobbies and crafts ,Travel, recreation and leisure - Abstract
I would just like to say thanks for the great advice from John Taffin. Clint Smith and the rest on going out and buying a gun for America. I did [...]
- Published
- 2005
6. I'll keep my .358, thanks
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Mill, Jon E.
- Subjects
Deer hunting -- Personal narratives ,Business ,Sport, sporting goods and toys industry - Abstract
I would like to thank you for the article on the .358 Win. ('Gun Notes,' 'The Great .358,' April 2004). My father gave me his Winchester Model 88 in .358 [...]
- Published
- 2004
7. RNA dysregulation in Amyotrophic Lateral Sclerosis
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Hawkins, S., Bhinge, Akshay, Mill, Jon, and Randall, Andrew
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Neurodegenerative disease ,ALS ,Amyotrophic Lateral Sclerosis ,RNA ,microRNA ,ePRINT - Abstract
Amyotrophic Lateral Sclerosis (ALS) is a devastating disease that results in progressive immobility and death of affected individuals. Paralysis is driven by the degeneration of motor neurons (MNs), the nerve cells that innervate muscle. Complex disease heterogeneity and incomplete understanding of the mechanisms driving ALS has resulted in poor therapeutic options. However, recent advances have uncovered common disruption to RNA processing events including: transcription, splicing, transport, translation and post-transcriptional repression. The mechanisms behind this dysregulation have yet to be fully elucidated. This thesis interrogates the roles of RNA regulators in ALS. We focus our attention on microRNAs (miRs) and RNA binding proteins (RBPs). MiRs are post-transcriptional regulators of gene expression, and are commonly disrupted in ALS. Using transcriptomic and bioinformatic analysis, we identified that miR-139 is downregulated in a majority of ALS cases. Exploration into the mechanism of action of this miR led us to discover a feedback loop between miR-139 and a key signalling pathway called WNT. We found that disruption of this feedback loop leads to WNT upregulation and MN degeneration in ALS. Transcriptomic analysis of patient tissue has revealed several microRNAs downregulated in ALS. As different miRs can converge on similar genes and/or pathways, we explored the role of ALS-miRs by inhibiting 44 microRNAs and analysing the downstream effects on cellular phenotypes. By conducting pathway analysis on their downstream targets, we uncovered convergence of ALS-associated miRs on RNA metabolism pathways, indicating their contribution to global disruption of RNA processing events. This also indicated that regulation of RBPs was occurring at the post-transcriptional level, altering protein expression. Completing protein screens is technically more difficult than genomic and transcriptomic analysis, due to the limited technology available. Current methods to assess RBP expression, activity and/or targets are low-throughput. To circumvent these limitations, we developed a novel method to obtain a holistic view of RBP-RNA interactions. Exonuclease-assisted mapping of protein-RNA interactions (ePRINT) captures a transcriptome wide view of all RBP interactions with all RNAs. We benchmarked ePRINT against gold-standard CLIP technologies, then demonstrated an application by applying ePRINT to our MN differentiation protocol. We identified RBPs involved in the cell fate transition between motor neuron progenitor (MNP) and post-mitotic MN. Importantly, we uncovered RBPs that had changes in activity, but not in RNA expression, meaning that ePRINT has the potential to uncover RBPs that contribute to ALS pathology, but have been missed by RNA analysis. Intervention or correction of dysregulated RNA regulators, such as miRs and RBPs discussed in this thesis, offer promising therapeutic targets for future ALS treatments.
- Published
- 2023
8. Epigenome-wide association study meta-analysis of aggressive behavior
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Dongen, Jenny, Suderman, Matthew, Sugden, Karen, Ismail, Khadeeja, Mulder, Rosa H., Kupper, Leanne K., Bustamante, Mariona, Alemany, Silvia, Bonder, Marc Jan, Parmar, Priyanka, Lowry, Estelle, Jansen, Rick, Baselmans, Bart, Nivard, Michel, Corcoran, David, Poulton, Richie, Mill, Jon, Hannon, Eilis, Arseneault, Louise, Vuoksimaa, Eero, Ollikainen, Miina, Corpeleijn, Eva, Ligthart, Lannie, Relton, Caroline, Moffitt, Terrie, Caspi, Avshalom, Jaakko Kaprio, Tiemeier, Henning, Snieder, Harold, Sunyer, Jordi, Franke, Lude, Sebert, Sylvain, Marjo-riitta, Bartels, Meike, Boomsma, Dorret, Reproductive Origins of Adult Health and Disease (ROAHD), Lifestyle Medicine (LM), Life Course Epidemiology (LCE), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), and Stem Cell Aging Leukemia and Lymphoma (SALL)
9. Investigating the disruption of transcriptional homeostatic networks in driving motor neuron specific degeneration in Amyotrophic Lateral Sclerosis
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Moran, J., Bhinge, Akshay, Mill, Jon, and Dempster, Emma
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ALS ,Amyotrophic lateral sclerosis ,Nociceptor ,Motor neuron ,Stem cell ,iPSC ,induced pluripotent stem cell ,human embryonic stem cell ,hESC ,Epigenetics ,RNA sequencing ,RNA seq ,Neuronal culture ,Calcium imaging ,CRISPR - Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease caused by the progressive loss of upper and lower motor neurons, eventually culminating in patient paralysis and death via asphyxiation. At the time of diagnosis, approximately 50% of patient motor neurons are predicted to have degenerated, resulting in a prognosis of 3-5 years. While most incidences of ALS are sporadic (~90%) with no obvious genetic constituent, approximately 10% of cases are inherited in a dominant manner and are referred to as familial ALS. At the present time there is no cure for ALS and current pharmacological treatments, such as Riluzole, operate with limited efficacy. As such, gaining further insight into pathomechanisms driving ALS is paramount for the development of novel and effective therapeutics. The C9ORF72 hexanucleotide repeat expansion is attributed to 40-50% of familial and approximately 10% of sporadic ALS cases. Investigating pathomechanisms driving familial cases of C9-ALS could elucidate neurodegenerative mechanisms central to both familial and sporadic cases. The aim of this thesis was to investigate transcriptional perturbations in C9-ALS to elucidate de novo candidates rendering motor neurons particularly susceptible to pathology. Evidence from previous studies suggested that nociceptors of ALS patients remain functionally viable due to the presence of non-neuropathic pain in approximately 80% of patients. We subsequently developed a novel protocol to efficiently generate functional sensory neuron cultures predominantly consisting of spinal nociceptors (~75%). Utilizing our protocol, we compared the transcriptomes of C9-ALS nociceptors with C9-ALS motor neurons which elucidated dysregulation of synaptic genes in motor neurons, potentially suggesting increased susceptibility of motor neurons to excitotoxic mechanisms. Finally, we utilised CRISPR systems employing dCas9 fused to epigenetic effectors to selectively demethylate the C9ORF72 repeat expansion and proximally associated regions to investigate epigenetic contributions to pathology. We observed an increase in transcript variant 3 expression and retention of intron 1 was observed upon demethylation of the repeat expansion. While increased expression of C9ORF72 could exacerbate pathomechanisms driven by RNA foci and accumulation of DPR proteins, deficits in synaptic function could be attenuated by reducing C9ORF72 haploinsufficiency. In summary, the work presented in this thesis outlines novel approaches to investigating the mechanisms driving pathology in C9-ALS with the hope of elucidating de novo candidates for therapeutic targeting. Furthermore, the ability to generate functional nociceptors broadens the scope of pain research permitting in vitro experiments to understand the mechanics of pain in human cells.
- Published
- 2022
10. That which does not kill us makes us stronger : differential sensitivity to metal exposure during zebrafish embryogenesis and the impact of pre-exposure on larval tolerance to subsequent stressors
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Robinson, P., Santos, Eduarda, Van Aerle, Ronny, Mill, Jon, and Dempster, Emma
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epigenetic ,hatching ,zebrafish ,development ,repeat exposure ,intermittent ,copper ,silver ,mercury ,methylmercury ,RNA ,ICP-MS - Abstract
Freshwater ecosystems are affected by pollution from many sources, impacting the biodiversity within. Exposures can be chronic, testing an organism's defence mechanisms over time, or intermittent, spiking in severity at point sources or as the seasons change. Despite these real-world scenarios being common, experimental studies often do not consider intermittent, repeated exposures within their designs. This could lead to a misinterpretation of safe concentrations within environments if these intermittent exposure conditions result in alterations of tolerance in the exposed organism. It is also important to understand how the life stage of the individual at the time of the exposures may impact their response, to both the initial and subsequent exposures. In this thesis, I set out to understand how chemical exposures during periods of sensitivity during development alter the responses to exposures at later stages, using zebrafish (Danio rerio) as a model species. I hypothesised that the first four hours of zebrafish development (one-cell stage to sphere stage) would be more sensitive to environmental stressors than exposures that are initiated after this point, due to developmental processes occurring during this time window including epigenetic reprogramming, zygotic genome activation and changes in chorion permeability. To test this, I used two pre-exposure time periods, one that included this proposed period of sensitivity (initiated at one-cell stage) and another initiating at four hours post fertilisation (sphere stage). I also proposed that the developmental stage directly after hatching would be a sensitive period due to the loss of the chorion membrane allowing for increased interactions with toxic chemicals within the exposure medium. Therefore, I used this period as the subsequent re-exposure period. To investigate these hypotheses, I used metals as the chemical stressors, specifically copper, silver and mercury. All are environmentally relevant as they are found to pollute aquatic environments around the globe, and their toxicity to fish has been studied, albeit rarely under these intermittent exposure scenarios. Silver can utilise some of the same uptake and cellular transport mechanisms as copper, however copper is an essential micronutrient whilst silver has no biological function, so comparisons of zebrafish embryo response were explored. Mercury, specifically methylmercury (due to the organic form's ability to bioaccumulate), was also used in this thesis as the metal has been shown to cause epigenetic alterations, has no biological function and is a widespread pollutant in many tropical environments. Pre-exposure to copper, regardless of whether that pre-exposure period encompassed the proposed period of sensitivity, increased the larval tolerance to re-exposure compared to naïve individuals. However, pre-exposure encompassing the hypothesised period of sensitivity was significantly more sensitive to copper during embryogenesis than pre-exposures initiated at four hours post fertilisation. The increased tolerance to re-exposure was associated with copper-induced delayed hatching, and increased tolerance was no longer observed when exposures were initiated in hatched larvae. The mechanisms responsible for the delay in hatching were explored, and hatching enzyme production was not shown to be disrupted. Addition of water containing hatching enzyme caused premature hatching in control treatment groups, whilst not initiating hatching in those pre-exposed. Therefore, I proposed that hatching enzyme binding sites on the chorion surface were affected by the copper exposures, resulting in reduced efficiency of the enzyme in causing chorion breakdown. Silver pre-exposures did not alter tolerance to re-exposure regardless of the pre-exposure period, despite the earlier exposure period that encompassed our proposed period of sensitivity being significantly more sensitive to silver exposure than the later pre-exposure period. The gene expression of several genes involved in the response to metal exposures and in epigenetic pathways were investigated at 48 hours post fertilisation, to determine if pre-exposure during either period altered gene regulation 24 hours after the exposure. No significant differences in gene expression were reported, which could have been due to the depuration period allowing gene expression to return to normal levels, or due to insufficient concentration of silver during the embryonic exposure. Zebrafish pre-exposed to methylmercury showed no significant mortality compared to controls and increased tolerance to subsequent exposures, principally lower mortality rates if the pre-exposure period encompassed the proposed period of sensitivity. Transcriptome profiles were investigated to understand how gene regulation differed between treatment groups and whether pre-exposure during epigenetic reprogramming had caused significant, long term alterations to gene regulation. In groups not re-exposed at larval stage, transcriptomes were very similar between controls and those pre-exposed, indicating as with the silver study that any potential gene expression alterations caused by the initial exposure return to baseline levels during depuration periods for these two metals. Upon re-exposure, those pre-exposed during embryogenesis showed significantly lower alterations of gene transcription, with pathways involved in apoptosis, immune response and DNA repair being less over/under-represented compared to naïve fish exposed to methylmercury for the first time. Naïve treatment groups, and to a lesser extent treatment groups pre-exposed to methylmercury during the later development stage, also showed suppression of pathways involved in nervous system and eye development, whilst zebrafish pre-exposed during the proposed sensitivity period did not. These results indicated that pre-exposure had decreased the impact of methylmercury exposure on gene regulation which could explain the decreased mortality observed. Differences in gene expression related to histones modification were also observed in all groups, suggesting that epigenetic alterations occur as a result of methylmercury exposure. I propose that these results provide support for a potential epigenetic mechanism associated with more efficient response to methylmercury during re-exposure and resulting in the increase in tolerance observed. My research highlights the importance of considering intermittent exposures in environmental risk assessment and conservation efforts, especially when determining the tolerance of fish species to pollutants. I also highlight the importance of initiating exposures as early in development as possible, to capture potential periods of increased sensitivity and to represent more closely real-world scenarios. This is especially prudent when exposures during this time can have more profound effects on embryos and/or affect their tolerance to subsequent exposures.
- Published
- 2022
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