A genetic variant of the sperm-specific SLO3 K+ channel has altered pH and Ca2+ sensitivities

To fertilize an oocyte, sperm must first undergo capacitation in which the sperm plasma membrane becomes hyperpolarized via activation of potassium (K(+)) channels and resultant K(+) efflux. Sperm-specific SLO3 K(+) channels are responsible for these membrane potential changes critical for fertilization in mouse sperm, and they are only sensitive to pH i However, in human sperm, the major K(+) conductance is both Ca(2+)- and pH i -sensitive. It has been debated whether Ca(2+)-sensitive SLO1 channels substitute for human SLO3 (hSLO3) in human sperm or whether human SLO3 channels have acquired Ca(2+) sensitivity. Here we show that hSLO3 is rapidly evolving and reveal a natural structural variant with enhanced apparent Ca(2+) and pH sensitivities. This variant allele (C382R) alters an amino acid side chain at a principal interface between the intramembrane-gated pore and the cytoplasmic gating ring of the channel. Because the gating ring contains sensors to intracellular factors such as pH and Ca(2+), the effectiveness of transduction between the gating ring and the pore domain appears to be enhanced. Our results suggest that sperm-specific genes can evolve rapidly and that natural genetic variation may have led to a SLO3 variant that differs from wild type in both pH and intracellular Ca(2+) sensitivities. Whether this physiological variation confers differences in fertility among males remains to be established.info:eu-repo/semantics/publishe

Non-power law constant flux solutions for the Smoluchowski coagulation equation

It is well known that for a large class of coagulation kernels, Smoluchowski coagulation equations have particular power law solutions which yield a constant flux of mass along all scales of the system. In this paper, we prove that for some choices of the coagulation kernels there are solutions with a constant flux of mass along all scales which are not power laws. The result is proved by means of a bifurcation argument.Comment: 35 page

Conserved mechanism of bicarbonate-induced sensitization of CatSper channels in human and mouse sperm

To fertilize an egg, mammalian sperm must undergo capacitation in the female genital tract. A key contributor to capacitation is the calcium (C

Multiple peak aggregations for the Keller-Segel system

In this paper we derive matched asymptotic expansions for a solution of the Keller-Segel system in two space dimensions for which the amount of mass aggregation is $8\pi N$, where $N=1,2,3,...$ Previously available asymptotics had been computed only for the case in which N=1

Stepwise Hydrogen Atom and Proton Transfers in Dioxygen Reduction by Aryl-Alcohol Oxidase

The mechanism of dioxygen reduction by the flavoenzyme aryl-alcohol oxidase was investigated with kinetic isotope, viscosity, and pL (pH/pD) effects in rapid kinetics experiments by stopped-flow spectrophotometry of the oxidative half-reaction of the enzyme. Double mixing of the enzyme in a stopped-flow spectrophotometer with [a-2H2]-p-methoxybenzyl alcohol and oxygen at varying aging times established a slow rate constant of 0.0023 s-1 for the wash-out of the D atom from the N5 atom of the reduced flavin. Thus, the deuterated substrate could be used to probe the cleavage of the N-H bond of the reduced flavin in the oxidative half-reaction. A significant and pH-independent substrate kinetic isotope effect (KIE) of 1.5 between pH 5.0 and 8.0 demonstrated that H transfer is partially limiting the oxidative half-reaction of the enzyme; a negligible solvent KIE of 1.0 between pD 5.0 and 8.0 proved a fast H+ transfer reaction that does not contribute to determining the flavin oxidation rates. Thus, a mechanism for dioxygen reduction in which the H atom originating from the reduced flavin and a H+ from a solvent exchangeable site are transferred in separate kinetic steps is proposed. The spectroscopic and kinetic data presented also showed a lack of stabilization of transient flavin intermediates. The substantial differences in the mechanistic details of O2 reduction by aryl-alcohol oxidase with respect to other alcohol oxidases like choline oxidase, pyranose 2-oxidase, and glucose oxidase further demonstrate the high level of versatility of the flavin cofactor in flavoenzymes

Molecular markers and allelic relationships of anthracnose resistance gene cluster B4 in common bean

Allelism tests and molecular marker analyses were combined to characterize the genes that, proceeding from the germplasm lines ‘A493’ and ‘A321’, confer resistance to bean anthracnose in the new breeding lines ‘A1220’ and ‘A1231’, respectively, developed through backcross breeding, using the dry bean landrace ‘Andecha’ as the recurrent parent. Allelism tests indicate that resistance to race 38 of anthracnose in genotypes ‘A1220’, ‘A1231’, and ‘BAT 93’ and in the differential cultivars ‘PI 207262’ and ‘Mexico 222’ is determined by different dominant alleles at the same locus. Therefore, the results obtained suggest that the so far considered as different genes Co-3 (described as present in ‘Mexico 222’) and Co-9 (described as present in ‘BAT 93’) are alleles of the same gene. RAPD markers OB12350, OAH181100, and OY171100 and SCAR markers SI19 and SW12 were found to be linked to the resistance gene. Data indicate that the resistance genes to race 38 present in these materials are alleles of the same R gene cluster located in linkage group B4, because markers OY171100, SI19 and SW12 were previously linked to this cluster. The SCAR markers SB12 and SAH18 were developed from RAPDs OB12350 and OAH181100, respectively, and a genetic map including the resistance gene and markers SB12, OY171100, SAH18, SW12 and SI19 was made using a F2 segregating population of 72 individuals derived from the cross ‘Andecha’ × ‘A493’

Genetic resistance to powdery mildew in common bean

Powdery mildew can cause severe yield losses in bean crops. Limited information about resistance sources, and nature and inheritance of resistance are available to bean breeders and plant pathologist. Sources of resistance were searched in seedling tests under controlled conditions in 44 well-known genotypes and in a Spanish germplasm core collection consisting on 201 accessions. A 0-4 scale was used to describe the infection types (IT) observed. Only six out of the 245 evaluated genotypes showed a complete resistance (IT0) without visible symptoms on the leaves: Amanda, Belneb, Cornell 49242, Negro San Luis, Porrillo Sintetico and the local accession BGE003161. Inheritance of resistance was studied in F and F segregating populations. Observed reactions in the five segregating populations fitted to Mendelian ratios with different modes of inheritance. Results revealed that cultivar Porrillo Sintetico carries two dominant and independent resistance genes: one gene conferring complete resistance (IT0), and another gene conferring IT3, characterized by a moderate mycelial development on the leaves. Both genes show a dominant epistatic relationship. Inheritance of response to powdery mildew in cv. Cornell 49242 was similar to cv. Porrillo Sintetico although the correspondence with the genes described in Porrillo Sintetico was not established. Line X2776 carries one dominant gene conferring IT3, and shares this gene with cv. Porrillo Sintetico. In cv. Amanda, two complementary genes appear to be involved in resistance to this fungus. This information will be relevant for the implementation of breeding programs focused on the development of cultivars carrying genetic resistance to powdery mildew