226 research outputs found
Algorithmic and Hardness Results for the Colorful Components Problems
In this paper we investigate the colorful components framework, motivated by
applications emerging from comparative genomics. The general goal is to remove
a collection of edges from an undirected vertex-colored graph such that in
the resulting graph all the connected components are colorful (i.e., any
two vertices of the same color belong to different connected components). We
want to optimize an objective function, the selection of this function
being specific to each problem in the framework.
We analyze three objective functions, and thus, three different problems,
which are believed to be relevant for the biological applications: minimizing
the number of singleton vertices, maximizing the number of edges in the
transitive closure, and minimizing the number of connected components.
Our main result is a polynomial time algorithm for the first problem. This
result disproves the conjecture of Zheng et al. that the problem is -hard
(assuming ). Then, we show that the second problem is -hard,
thus proving and strengthening the conjecture of Zheng et al. that the problem
is -hard. Finally, we show that the third problem does not admit
polynomial time approximation within a factor of for
any , assuming (or within a factor of , assuming ).Comment: 18 pages, 3 figure
Male Infertility is a Women\u27s Health Issue-Research and Clinical Evaluation of Male Infertility Is Needed
Infertility is a devastating experience for both partners as they try to conceive. Historically, when a couple could not conceive, the woman has carried the stigma of infertility; however, men and women are just as likely to contribute to the couple\u27s infertility. With the development of assisted reproductive technology (ART), the treatment burden for male and unexplained infertility has fallen mainly on women. Equalizing this burden requires reviving research on male infertility to both improve treatment options and enable natural conception. Despite many scientific efforts, infertility in men due to sperm dysfunction is mainly diagnosed by a semen analysis. The semen analysis is limited as it only examines general sperm properties such as concentration, motility, and morphology. A diagnosis of male infertility rarely includes an assessment of internal sperm components such as DNA, which is well documented to have an impact on infertility, or other components such as RNA and centrioles, which are beginning to be adopted. Assessment of these components is not typically included in current diagnostic testing because available treatments are limited. Recent research has expanded our understanding of sperm biology and suggests that these components may also contribute to the failure to achieve pregnancy. Understanding the sperm\u27s internal components, and how they contribute to male infertility, would provide avenues for new therapies that are based on treating men directly for male infertility, which may enable less invasive treatments and even natural conception
Plk1/Polo Phosphorylates Sas-4 at the Onset of Mitosis for an Efficient Recruitment of Pericentriolar Material to Centrosomes
Centrosomes are the major microtubule-organizing centers, consisting of centrioles surrounded by a pericentriolar material (PCM). Centrosomal PCM is spatiotemporally regulated to be minimal during interphase and expands as cells enter mitosis. It is unclear how PCM expansion is initiated at the onset of mitosis. Here, we identify that, in Drosophila, Plk1/Polo kinase phosphorylates the conserved centrosomal protein Sas-4 in vitro. This phosphorylation appears to occur at the onset of mitosis, enabling Sas-4's localization to expand outward from meiotic and mitotic centrosomes. The Plk1/Polo kinase site of Sas-4 is then required for an efficient recruitment of Cnn and gamma-tubulin, bona fide PCM proteins that are essential for PCM expansion and centrosome maturation. Point mutations at Plk1/Polo sites of Sas-4 affect neither centrosome structure nor centriole duplication but specifically reduce the affinity to bind Cnn and gamma-tubulin. These observations identify Plk1/Polo kinase regulation of Sas-4 as essential for efficient PCM expansion
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Tubulin nucleotide status controls Sas-4-dependent pericentriolar material recruitment
Regulated centrosome biogenesis is required for accurate cell division and for maintaining genome integrity1. Centrosomes consist of a centriole pair surrounded by a protein network known as pericentriolar material (PCM)1. PCM assembly is a tightly regulated, critical step that determines a centrosome’s size and capability2–4. Here, we report a role for tubulin in regulating PCM recruitment via the conserved centrosomal protein Sas-4. Tubulin directly binds to Sas-4; together they are components of cytoplasmic complexes of centrosomal proteins5,6. A Sas-4 mutant, which cannot bind tubulin, enhances centrosomal protein complex formation and has abnormally large centrosomes with excessive activity. These suggest that tubulin negatively regulates PCM recruitment. Whereas tubulin-GTP prevents Sas-4 from forming protein complexes, tubulin-GDP promotes it. Thus, tubulin’s regulation of PCM recruitment depends on its GTP/GDP-bound state. These results identify a role for tubulin in regulating PCM recruitment independent of its well-known role as a building block of microtubules7. Based on its guanine bound state, tubulin can act as a molecular switch in PCM recruitment
Sperm centriole assessment identifies male factor infertility in couples with unexplained infertility - a pilot study
Unexplained infertility affects about one-third of infertile couples and is defined as the failure to identify the cause of infertility despite extensive evaluation of the male and female partners. Therefore, there is a need for a multiparametric approach to study sperm function. Recently, we developed a Fluorescence-Based Ratiometric Analysis of Sperm Centrioles (FRAC) assay to determine sperm centriole quality. Here, we perform a pilot study of sperm from 10 fertile men and 10 men in couples with unexplained infertility, using three centriolar biomarkers measured at three sperm locations from two sperm fractions, representing high and low sperm quality. We found that FRAC can identify men from couples with unexplained infertility as the likely source of infertility. Higher quality fractions from 10 fertile individuals were the reference population. All 180 studied FRAC values in the 10 fertile individuals fell within the reference population range. Eleven of the 180 studied FRAC values in the 10 infertile patients were outliers beyond the 95% confidence intervals (P = 0.0008). Three men with unexplained infertility had outlier FRAC values in their higher quality sperm fraction, while four had outlier FRAC values in their lower quality sperm fraction (3/10 and 4/10, P = 0.060 and P = 0.025, respectively), suggesting that these four individuals are infertile due, in part, to centriolar defects. We propose that a larger scale study should be performed to determine the ability of FRAC to identify male factor infertility and its potential contribution to sperm multiparametric analysis
Two-Dimensional Wetting of a Stepped Copper Surface.
Highly corrugated, stepped surfaces present regular 1D arrays of binding sites, creating a complex, heterogeneous environment to water. Rather than decorating the hydrophilic step sites to form 1D chains, water on stepped Cu(511) forms an extended 2D network that binds strongly to the steps but bridges across the intervening hydrophobic Cu(100) terraces. The hydrogen-bonded network contains pentamer, hexamer, and octomer water rings that leave a third of the stable Cu step sites unoccupied in order to bind water H down close to the step dipole and complete three hydrogen bonds per molecule.Herchel Smith fun
Note: A simple sample transfer alignment for ultra-high vacuum systems
The alignment of ultra-high-vacuum sample transfer systems can be problematic when there is no direct line of sight to assist the user. We present the design of a simple and cheap system which greatly simplifies the alignment of sample transfer devices. Our method is based on the adaptation of a commercial digital camera which provides live views from within the vacuum chamber. The images of the camera are further processed using an image recognition and processing code which determines any misalignments and reports them to the user. Installation has proven to be extremely useful in order to align the sample with respect to the transfer mechanism. Furthermore, the alignment software can be easily adapted for other systems.One of us (A.T.) acknowledges financial support provided by the FWF (Austrian Science Fund) within Project No. J3479-N20
Algorithms for Cut Problems on Trees
We study the {\sc multicut on trees} and the {\sc generalized multiway Cut on
trees} problems. For the {\sc multicut on trees} problem, we present a
parameterized algorithm that runs in time , where is the positive root of the polynomial
. This improves the current-best algorithm of Chen et al. that runs
in time . For the {\sc generalized multiway cut on trees}
problem, we show that this problem is solvable in polynomial time if the number
of terminal sets is fixed; this answers an open question posed in a recent
paper by Liu and Zhang. By reducing the {\sc generalized multiway cut on trees}
problem to the {\sc multicut on trees} problem, our results give a
parameterized algorithm that solves the {\sc generalized multiway cut on trees}
problem in time , where time
Mediation of adenylyl cyclase sensitization by PTX-insensitive Gα oA , Gα i1 , Gα i2 or Gα i3
Chronic activation of mu-opioid receptors, which couple to pertussis toxin-sensitive Gα i/o proteins to inhibit adenylyl cyclase (AC), leads to a compensatory sensitization of AC. Pertussis toxin-insensitive mutations of Gα i/o subtypes, in which the pertussis toxin-sensitive cysteine is mutated to isoleucine (G ), were used to determine whether each of the Gα i/o subtypes is able to mediate sensitization of AC. G , G , G or G were individually transiently transfected into C6 glioma cells stably expressing the mu-opioid receptor, or transiently co-expressed with the mu-opioid receptor into human embryonic kidney (HEK)293T cells. Cells were treated with pertussis toxin to uncouple endogenous Gα i/o proteins, followed by acute or chronic treatment with the mu-opioid agonist, [D-Ala 2 ,N-Me-Phe 4 ,Gly 5 -ol]enkephalin (DAMGO). Each Gα i/o subtype mediated acute DAMGO inhibition of AC and DAMGO-induced sensitization of AC. The potency for DAMGO to stimulate sensitization was independent of the Gα i/o subtype, but the level of sensitization was increased in clones expressing higher levels of Gα i/o subunits. Sensitization of AC mediated by a component of fetal bovine serum, which was also dependent on the level of functional Gα i/o subunits in the cell, was observed. This serum-mediated sensitization partially masked mu-opioid-mediated sensitization when expressed as percentage overshoot due to an apparent increase in AC activity.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65707/1/j.1471-4159.2006.04176.x.pd
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