45 research outputs found

    Disjointness Graphs of segments in R^2 are almost all Hamiltonian

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    Let P be a set of n >= 2 points in general position in R^2. The edge disjointness graph D(P) of P is the graph whose vertices are all the closed straight line segments with endpoints in P, two of which are adjacent in D(P) if and only if they are disjoint. In this note, we give a full characterization of all those edge disjointness graphs that are hamiltonian. More precisely, we shall show that (up to order type isomorphism) there are exactly 8 instances of P for which D(P) is not hamiltonian. Additionally, from one of these 8 instances, we derive a counterexample to a criterion for the existence of hamiltonian cycles due to A. D. Plotnikov in 1998

    Point sets that minimize (≀k)(\le k)-edges, 3-decomposable drawings, and the rectilinear crossing number of K30K_{30}

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    There are two properties shared by all known crossing-minimizing geometric drawings of KnK_n, for nn a multiple of 3. First, the underlying nn-point set of these drawings has exactly 3(k+22)3\binom{k+2}{2} (≀k)(\le k)-edges, for all 0≀k<n/30\le k < n/3. Second, all such drawings have the nn points divided into three groups of equal size; this last property is captured under the concept of 3-decomposability. In this paper we show that these properties are tightly related: every nn-point set with exactly 3(k+22)3\binom{k+2}{2} (≀k)(\le k)-edges for all 0≀k<n/30\le k < n/3, is 3-decomposable. As an application, we prove that the rectilinear crossing number of K30K_{30} is 9726.Comment: 14 page

    Congenital Hypogonadotropic Hypogonadism Due to GNRH Receptor Mutations in Three Brothers Reveal Sites Affecting Conformation and Coupling

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    Congenital hypogonadotropic hypogonadism (CHH) is characterized by low gonadotropins and failure to progress normally through puberty. Mutations in the gene encoding the GnRH receptor (GNRHR1) result in CHH when present as compound heterozygous or homozygous inactivating mutations. This study identifies and characterizes the properties of two novel GNRHR1 mutations in a family in which three brothers display normosmic CHH while their sister was unaffected. Molecular analysis in the proband and the affected brothers revealed two novel non-synonymous missense GNRHR1 mutations, present in a compound heterozygous state, whereas their unaffected parents possessed only one inactivating mutation, demonstrating the autosomal recessive transmission in this kindred and excluding X-linked inheritance equivocally suggested by the initial pedigree analysis. The first mutation at c.845 C>G introduces an Arg substitution for the conserved Pro 282 in transmembrane domain (TMD) 6. The Pro282Arg mutant is unable to bind radiolabeled GnRH analogue. As this conserved residue is important in receptor conformation, it is likely that the mutation perturbs the binding pocket and affects trafficking to the cell surface. The second mutation at c.968 A>G introduces a Cys substitution for Tyr 323 in the functionally crucial N/DPxxY motif in TMD 7. The Tyr323Cys mutant has an increased GnRH binding affinity but reduced receptor expression at the plasma membrane and impaired G protein-coupling. Inositol phosphate accumulation assays demonstrated absent and impaired Gαq/11 signal transduction by Pro282Arg and Tyr323Cys mutants, respectively. Pretreatment with the membrane permeant GnRHR antagonist NBI-42902, which rescues cell surface expression of many GNRHR1 mutants, significantly increased the levels of radioligand binding and intracellular signaling of the Tyr323Cys mutant but not Pro282Arg. Immunocytochemistry confirmed that both mutants are present on the cell membrane albeit at low levels. Together these molecular deficiencies of the two novel GNRHR1 mutations lead to the CHH phenotype when present as a compound heterozygote

    On the connectivity of the disjointness graph of segments of point sets in general position in the plane

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    Let PP be a set of n≄3n\geq 3 points in general position in the plane. The edge disjointness graph D(P)D(P) of PP is the graph whose vertices are all the closed straight line segments with endpoints in PP, two of which are adjacent in D(P)D(P) if and only if they are disjoint. We show that the connectivity of D(P)D(P) is at least (⌊n−22⌋2)+(⌈n−22⌉2)\binom{\lfloor\frac{n-2}{2}\rfloor}{2}+\binom{\lceil\frac{n-2}{2}\rceil}{2}, and that this bound is tight for each n≄3n\geq 3.Comment: 13 pages, 5 figure
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