207 research outputs found
A continuous model for microtubule dynamics with catastrophe, rescue and nucleation processes
Microtubules are a major component of the cytoskeleton distinguished by
highly dynamic behavior both in vitro and in vivo. We propose a general
mathematical model that accounts for the growth, catastrophe, rescue and
nucleation processes in the polymerization of microtubules from tubulin dimers.
Our model is an extension of various mathematical models developed earlier
formulated in order to capture and unify the various aspects of tubulin
polymerization including the dynamic instability, growth of microtubules to
saturation, time-localized periods of nucleation and depolymerization as well
as synchronized oscillations exhibited by microtubules under various
experimental conditions. Our model, while attempting to use a minimal number of
adjustable parameters, covers a broad range of behaviors and has predictive
features discussed in the paper. We have analyzed the resultant behaviors of
the microtubules changing each of the parameter values at a time and observing
the emergence of various dynamical regimes.Comment: 25 pages, 12 figure
Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells
Remodelling of mitochondrial metabolism is a hallmark of cancer. Mutations in the genes encoding succinate dehydrogenase (SDH), a key Krebs cycle component, are associated with hereditary predisposition to pheochromocytoma and paraganglioma, through mechanisms which are largely unknown. Recently, the jumonji-domain histone demethylases have emerged as a novel family of 2-oxoglutarate-dependent chromatin modifiers with credible functions in tumourigenesis. Using pharmacological and siRNA methodologies we show that increased methylation of histone H3 is a general consequence of SDH loss-of-function in cultured mammalian cells and can be reversed by overexpression of the JMJD3 histone demethylase. ChIP analysis revealed that the core promoter of IGFBP7, which encodes a secreted protein upregulated after loss of SDHB, showed decreased occupancy by H3K27me3 in the absence of SDH. Finally, we provide the first evidence that the chief (type I) cell is the major methylated histone-immunoreactive constituent of paraganglioma. These results support the notion that loss of mitochondrial function alters epigenetic processes and might provide a signature methylation mark for paraganglioma
Analysis of a microscopic stochastic model of microtubule dynamic instability
A novel theoretical model of dynamic instability of a system of linear (1D)
microtubules (MTs) in a bounded domain is introduced for studying the role of a
cell edge in vivo and analyzing the effect of competition for a limited amount
of tubulin. The model differs from earlier models in that the evolution of MTs
is based on the rates of single unit (e.g., a heterodimer per protofilament)
transformations, in contrast to postulating effective rates/frequencies of
larger-scale changes, extracted, e.g., from the length history plots of MTs.
Spontaneous GTP hydrolysis with finite rate after polymerization is assumed,
and theoretical estimates of an effective catastrophe frequency as well as
other parameters characterizing MT length distributions and cap size are
derived. We implement a simple cap model which does not include vectorial
hydrolysis. We demonstrate that our theoretical predictions, such as steady
state concentration of free tubulin, and parameters of MT length distributions,
are in agreement with the numerical simulations. The present model establishes
a quantitative link between microscopic parameters governing the dynamics of
MTs and macroscopic characteristics of MTs in a closed system. Lastly, we use a
computational Monte Carlo model to provide an explanation for non-exponential
MT length distributions observed in experiments. In particular, we show that
appearance of such non-exponential distributions in the experiments can occur
because the true steady state has not been reached, and/or due to the presence
of a cell edge.Comment: 14 pages, 7 figure
Influence of Stream Location in a Drainage Network on the Index of Biotic Integrity
The index of biotic integrity (IBI) has become a widely used tool for assessing the condition of stream fish communities and the overall biological status of streams. Because the location of a stream in a drainage network can influence the species richness offish communities and because species richness is an important component of the IBI, we examined the influence of stream spatial location on the IBI. We found that IBI scores for headwater streams in three Illinois drainage basins were significantly lower than those calculated for tributary streams of similar size connecting directly to larger streams. This difference in IBI was related to the increased species richness and to a greater number of sucker and darter species in tributaries that drain into larger, mainâchannel streams. Because of the influence of tributary location on the IBI, expected values for headwater tributary streams should be developed independently from those developed for mainâchannel tributary streams. Failure to do so can result in a substantial underestimation of the IBI of headwater tributary streams or an overestimation of mainâchannel tributaries.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/142315/1/tafs0635.pd
Does the understanding of complex dynamic events at 10 months predict vocabulary development?
By the end of their first year, infants can interpret many different types of complex dynamic visual events, such as caused-motion, chasing, and goal-directed action. Infants of this age are also in the early stages of vocabulary development, producing their first words at around 12 months. The present work examined whether there are meaningful individual differences in infantsâ ability to represent dynamic causal events in visual scenes, and whether these differences influence vocabulary development. As part of the longitudinal Language 0â5 Project, 78 10-month-old infants were tested on their ability to interpret three dynamic motion events, involving (a) caused-motion, (b) chasing behaviour, and (c) goal-directed movement. Planned analyses found that infants showed evidence of understanding the first two event types, but not the third. Looking behaviour in each task was not meaningfully related to vocabulary development, nor were there any correlations between the tasks. The results of additional exploratory analyses and simulations suggested that the infantsâ understanding of each event may not be predictive of their vocabulary development, and that looking times in these tasks may not be reliably capturing any meaningful individual differences in their knowledge. This raises questions about how to convert experimental group designs to individual differences measures, and how to interpret infant looking time behaviour
Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma
BACKGROUND: Mitochondrial succinate dehydrogenase (SDH) is a component of both the tricarboxylic acid cycle and the electron transport chain. Mutations of SDHD, the first protein of intermediary metabolism shown to be involved in tumorigenesis, lead to the human tumors paraganglioma (PGL) and pheochromocytoma (PC). SDHD is remarkable in showing an 'imprinted' tumor suppressor phenotype. Mutations of SDHD show a very high penetrance in man and we postulated that knockout of Sdhd would lead to the development of PGL/PC, probably in aged mice. METHODOLOGY/PRINCIPAL FINDINGS: We generated a conventional knockout of Sdhd in the mouse, removing the entire third exon. We also crossed this mouse with a knockout of H19, a postulated imprinted modifier gene of Sdhd tumorigenesis, to evaluate if loss of these genes together would lead to the initiation or enhancement of tumor development. Homozygous knockout of Sdhd results in embryonic lethality. No paraganglioma or other tumor development was seen in Sdhd KO mice followed for their entire lifespan, in sharp contrast to the highly penetrant phenotype in humans. Heterozygous Sdhd KO mice did not show hyperplasia of paraganglioma-related tissues such as the carotid body or of the adrenal medulla, or any genotype-related pathology, with similar body and organ weights to wildtype mice. A cohort of Sdhd/H19 KO mice developed several cases of profound cardiac hypertrophy, but showed no evidence of PGL/PC. CONCLUSIONS: Knockout of Sdhd in the mouse does not result in a disease phenotype. H19 may not be an initiator of PGL/PC tumorigenesis
The first Dutch SDHB founder deletion in paraganglioma â pheochromocytoma patients
Contains fulltext :
81280.pdf (publisher's version ) (Open Access)BACKGROUND: Germline mutations of the tumor suppressor genes SDHB, SDHC and SDHD play a major role in hereditary paraganglioma and pheochromocytoma. These three genes encode subunits of succinate dehydrogenase (SDH), the mitochondrial tricarboxylic acid cycle enzyme and complex II component of the electron transport chain. The majority of variants of the SDH genes are missense and nonsense mutations. To date few large deletions of the SDH genes have been described. METHODS: We carried out gene deletion scanning using MLPA in 126 patients negative for point mutations in the SDH genes. We then proceeded to the molecular characterization of deletions, mapping breakpoints in each patient and used haplotype analysis to determine whether the deletions are due to a mutation hotspot or if a common haplotype indicated a single founder mutation. RESULTS: A novel deletion of exon 3 of the SDHB gene was identified in nine apparently unrelated Dutch patients. An identical 7905 bp deletion, c.201-4429_287-933del, was found in all patients, resulting in a frameshift and a predicted truncated protein, p.Cys68HisfsX21. Haplotype analysis demonstrated a common haplotype at the SDHB locus. Index patients presented with pheochromocytoma, extra-adrenal PGL and HN-PGL. A lack of family history was seen in seven of the nine cases. CONCLUSION: The identical exon 3 deletions and common haplotype in nine patients indicates that this mutation is the first Dutch SDHB founder mutation. The predominantly non-familial presentation of these patients strongly suggests reduced penetrance. In this small series HN-PGL occurs as frequently as pheochromocytoma and extra-adrenal PGL
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