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1.
J Evol Biol ; 29(11): 2289-2296, 2016 11.
Article in English | MEDLINE | ID: mdl-27488082

ABSTRACT

Ejaculated proteins play important roles in reproductive fitness. In many species, seminal fluid coagulates and forms what has been referred to as a copulatory plug in the female's reproductive tract. In mice, previous work demonstrated that knockout males missing a key seminal fluid protein were unable to form a plug and less successful at siring litters in noncompetitive matings (one female, one male), probably the result of reduced sperm transport or insufficient stimulation of the female. Here, we extend these previous studies to competitive matings (one female, two males) and make two key insights. First, when first males were unable to form a plug, they lost almost all paternity to second males to mate. Thus, the copulatory plugs of second males could not rescue the reduced fertility of first males. Second, we showed that the copulatory plug of first males effectively blocked fertilization by second males, even if first males were vasectomized. Taken together, our experiments demonstrated that first males lost almost all paternity if they never formed a plug. We discuss our results in the context of natural populations, where in spite of the strong effects seen here, pregnant female mice regularly carry litters fertilized by more than one male.


Subject(s)
Copulation , Spermatozoa , Animals , Female , Male , Mice , Paternity , Pregnancy , Reproduction , Sexual Behavior, Animal
2.
PLoS One ; 7(11): e49387, 2012.
Article in English | MEDLINE | ID: mdl-23185324

ABSTRACT

Rab monomeric GTPases regulate specific aspects of vesicle transport in eukaryotes including coat recruitment, uncoating, fission, motility, target selection and fusion. Moreover, individual Rab proteins function at specific sites within the cell, for example the ER, golgi and early endosome. Importantly, the localization and function of individual Rab subfamily members are often conserved underscoring the significant contributions that model organisms such as Caenorhabditis elegans can make towards a better understanding of human disease caused by Rab and vesicle trafficking malfunction. With this in mind, a bioinformatics approach was first taken to identify and classify the complete C. elegans Rab family placing individual Rabs into specific subfamilies based on molecular phylogenetics. For genes that were difficult to classify by sequence similarity alone, we did a comparative analysis of intron position among specific subfamilies from yeast to humans. This two-pronged approach allowed the classification of 30 out of 31 C. elegans Rab proteins identified here including Rab31/Rab50, a likely member of the last eukaryotic common ancestor (LECA). Second, a molecular toolset was created to facilitate research on biological processes that involve Rab proteins. Specifically, we used Gateway-compatible C. elegans ORFeome clones as starting material to create 44 full-length, sequence-verified, dominant-negative (DN) and constitutive active (CA) rab open reading frames (ORFs). Development of this toolset provided independent research projects for students enrolled in a research-based molecular techniques course at California State University, East Bay (CSUEB).


Subject(s)
Caenorhabditis elegans Proteins/classification , Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/enzymology , Computational Biology/methods , Multigene Family , rab GTP-Binding Proteins/classification , rab GTP-Binding Proteins/metabolism , Amino Acid Sequence , Animals , Caenorhabditis elegans Proteins/chemistry , Clone Cells , Conserved Sequence/genetics , Humans , Introns/genetics , Molecular Sequence Data , Open Reading Frames/genetics , Phylogeny , RNA Splicing/genetics , Reproducibility of Results , Sequence Alignment , rab GTP-Binding Proteins/chemistry
3.
Emerg Infect Dis ; 16(9): 1388-95, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20735922

ABSTRACT

We compared confirmed pandemic (H1N1) 2009 influenza and seasonal influenza diagnosed in Western Australia during the 2009 influenza season. From 3,178 eligible reports, 984 pandemic and 356 seasonal influenza patients were selected; 871 (88.5%) and 288 (80.9%) were interviewed, respectively. Patients in both groups reported a median of 6 of 11 symptoms; the difference between groups in the proportion reporting any given symptom was < or =10%. Fewer than half the patients in both groups had > or =1 underlying condition, and only diabetes was associated with pandemic (H1N1) 2009 influenza (odds ratio [OR] 1.9, 95% confidence interval [CI] 1.1-3.5). A total of 129 (14.8%) persons with pandemic (H1N1) 2009 and 36 (12.5%) persons with seasonal influenza were hospitalized (p = 0.22). After controlling for age, we found that patient hospitalization was associated with pandemic (H1N1) 2009 influenza (OR 1.5; 95% CI 1.1-2.1). Contemporaneous pandemic and seasonal influenza infections were substantially similar in terms of patients' symptoms, risk factors, and proportion hospitalized.


Subject(s)
Influenza A Virus, H1N1 Subtype , Influenza, Human/epidemiology , Pandemics , Adolescent , Adult , Aged , Child , Child, Preschool , Diabetes Complications/epidemiology , Female , Humans , Infant , Infant, Newborn , Influenza, Human/complications , Male , Middle Aged , Risk Factors , Seasons , Western Australia/epidemiology , Young Adult
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