93 research outputs found
First Record of the True Katydid, \u3ci\u3ePterophylla Camellifolia\u3c/i\u3e (Orthoptera: Tettigoniidae: Pseudophyllinae) in North Dakota
The true katydid, Pterophylla camellifolia, is recorded as a new state record for North Dakota
A List of the Beetles of South Dakota
A checklist of beetles of South Dakota has been compiled from records from the following sources: the South Dakota State University Insect Collection, which consists of 325 Cornell drawers of Coleoptera; records in the senior author\u27s personal collection, which consists of 84 Schmitt boxes of Coleoptera; and scattered literature citations. The checklist contains the scientific names for the beetle species; their common names, when given; localities in the state where the species had been collected, dates of collection, and ecological notes such as host plants, how collected, or habitat, when known. Sixty-nine families of beetles, including 695 genera and 1,955 species and subspecies, have been collected in South Dakota
Preparation of a Future Homemakers of America Chapter Handbook for Local Chapters in South Dakota
The purpose of this study was to provide a Future Homemakers of America (hereafter referred to as FHA) handbook for South Dakota which would assist officers, and advisers in carrying out chapter, state, and national association responsibilities. The South Dakota Association of FHA is an organization affiliated with the national association. All information from the national office is channeled to the state FHA adviser, who in turn uses the material as a method of communication with the region and local chapters. Before this study, all communiques sent by the state FHA adviser were in the form of loose sheets. Upon receiving the loose sheets, local chapters used their own method of organizing and filing the material for later use. In that the author developed a real interest in FHA as the result of having been a chapter adviser for four years, Suite Chapter Adviser for one year and having been adviser to a state officer, she realized the need for organizing all FHA material for the local chapter
Proteomic interrogation of the meninges reveals the molecular identities of structural components and regional distinctions along the CNS axis
Par3 Controls Epithelial Spindle Orientation by aPKC-Mediated Phosphorylation of Apical Pins
SummaryBackgroundFormation of epithelial sheets requires that cell division occurs in the plane of the sheet. During mitosis, spindle poles align so the astral microtubules contact the lateral cortex. Confinement of the mammalian Pins protein to the lateral cortex is essential for this process. Defects in signaling through Cdc42 and atypical protein kinase C (aPKC) also cause spindle misorientation. When epithelial cysts are grown in 3D cultures, misorientation creates multiple lumens.ResultsWe now show that silencing of the polarity protein Par3 causes spindle misorientation in Madin-Darby canine kidney cell cysts. Silencing of Par3 also disrupts aPKC association with the apical cortex, but expression of an apically tethered aPKC rescues normal lumen formation. During mitosis, Pins is mislocalized to the apical surface in the absence of Par3 or by inhibition of aPKC. Active aPKC increases Pins phosphorylation on Ser401, which recruits 14-3-3 protein. 14-3-3 binding inhibits association of Pins with Gαi, through which Pins attaches to the cortex. A Pins S401A mutant mislocalizes over the cell cortex and causes spindle orientation and lumen defects.ConclusionsThe Par3 and aPKC polarity proteins ensure correct spindle pole orientation during epithelial cell division by excluding Pins from the apical cortex. Apical aPKC phosphorylates Pins, which results in the recruitment of 14-3-3 and inhibition of binding to Gαi, so the Pins falls off the cortex. In the absence of a functional exclusion mechanism, astral microtubules can associate with Pins over the entire epithelial cortex, resulting in randomized spindle pole orientation
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DNA-mediated association of two histone-bound complexes of yeast Chromatin Assembly Factor-1 (CAF-1) drives tetrasome assembly in the wake of DNA replication.
Nucleosome assembly in the wake of DNA replication is a key process that regulates cell identity and survival. Chromatin assembly factor 1 (CAF-1) is a H3-H4 histone chaperone that associates with the replisome and orchestrates chromatin assembly following DNA synthesis. Little is known about the mechanism and structure of this key complex. Here we investigate the CAF-1•H3-H4 binding mode and the mechanism of nucleosome assembly. We show that yeast CAF-1 binding to a H3-H4 dimer activates the Cac1 winged helix domain interaction with DNA. This drives the formation of a transient CAF-1•histone•DNA intermediate containing two CAF-1 complexes, each associated with one H3-H4 dimer. Here, the (H3-H4
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The Cac1 subunit of histone chaperone CAF-1 organizes CAF-1-H3/H4 architecture and tetramerizes histones.
The histone chaperone Chromatin Assembly Factor 1 (CAF-1) deposits tetrameric (H3/H4)2 histones onto newly-synthesized DNA during DNA replication. To understand the mechanism of the tri-subunit CAF-1 complex in this process, we investigated the protein-protein interactions within the CAF-1-H3/H4 architecture using biophysical and biochemical approaches. Hydrogen/deuterium exchange and chemical cross-linking coupled to mass spectrometry reveal interactions that are essential for CAF-1 function in budding yeast, and importantly indicate that the Cac1 subunit functions as a scaffold within the CAF-1-H3/H4 complex. Cac1 alone not only binds H3/H4 with high affinity, but also promotes histone tetramerization independent of the other subunits. Moreover, we identify a minimal region in the C-terminus of Cac1, including the structured winged helix domain and glutamate/aspartate-rich domain, which is sufficient to induce (H3/H4)2 tetramerization. These findings reveal a key role of Cac1 in histone tetramerization, providing a new model for CAF-1-H3/H4 architecture and function during eukaryotic replication
Phylogenetic Relationships of Tribes Within Harpalinae (Coleoptera: Carabidae) as Inferred from 28S Ribosomal DNA and the Wingless Gene
Harpalinae is a large, monophyletic subfamily of carabid ground beetles containing more than 19,000 species in approximately 40 tribes. The higher level phylogenetic relationships within harpalines were investigated based on nucleotide data from two nuclear genes, wingless and 28S rDNA. Phylogenetic analyses of combined data indicate that many harpaline tribes are monophyletic, however the reconstructed trees showed little support for deeper nodes. In addition, our results suggest that the Lebiomorph Assemblage (tribes Lebiini, Cyclosomini, Graphipterini, Perigonini, Odacanthini, Lachnophorini, Pentagonicini, Catapiesini and Calophaenini), which is united by a morphological synapomorphy, is not monophyletic, and the tribe Lebiini is paraphyletic with respect to members of Cyclosomini. Two unexpected clades of tribes were supported: the Zuphiitae, comprised of Anthiini, Zuphiini, Helluonini, Dryptini, Galeritini, and Physocrotaphini; and a clade comprised of Orthogoniini, Pseudomorphini, and Graphipterini. The data presented in this study represent a dense sample of taxa to examine the molecular phylogeny of Harpalinae and provide a useful framework to examine the origin and evolution of morphological and ecological diversity in this group
Distributions For 2 Holarctic Weevils Which Are New Household Pests
Volume: 99Start Page: 102End Page: 10
Primary Type Specimens In The South dakota State University Usa Insect Collection
Volume: 88Start Page: 43End Page: 4
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