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141.
Ilana Chefetz Edward Grimley Kun Yang Linda Hong Ekaterina V. Vinogradova Radu Suciu Ilya Kovalenko David Karnak Cynthia A. Morgan Mikhail Chtcherbinine Cameron Buchman Brandt Huddle Scott Barraza Meredith Morgan Kara A. Bernstein Euisik Yoon David B. Lombard Andrea Bild Ronald J. Buckanovich 《Cell reports》2019,26(11):3061-3075.e6
142.
Tomofumi Tadauchi Cynthia Lam Laura Liu Yizhou Zhou Danming Tang Salina Louie Brad Snedecor Shahram Misaghi 《Biotechnology progress》2019,35(2):e2772
Chinese hamster ovary (CHO) cells are conventionally used to generate therapeutic cell lines via random integration (RI), where desired transgenes are stably integrated into the genome. Targeted integration (TI) approaches, which involve integration of a transgene into a specific locus in the genome, are increasingly utilized for CHO cell line development (CLD) in recent years. None of these CLD approaches, however, are suitable for expression of toxic or difficult-to-express molecules, or for determining the underlying causes for poor expression of some molecules. Here we introduce a regulated target integration (RTI) system, where the desired transgene is integrated into a specific locus and transcribed under a regulated promoter. This system was used to determine the underlying causes of low protein expression for a difficult-to-express antibody (mAb-A). Interestingly, we observed that both antibody heavy chain (HC) and light chain (LC) subunits of mAb-A independently contributed to its low expression. Analysis of RTI cell lines also revealed that while mAb-A LC triggered accumulation of intracellular BiP, its HC displayed impaired degradation and clearance. RTI pools, generated by swapping the WT or point-mutant versions of difficult-to-express antibody HC and LC with that of an average antibody, were instrumental in understanding the contribution of HC and LC subunits to the overall antibody expression. The ability to selectively turn off the expression of a target transgene in an RTI system could help to directly link expression of a transgene to an observed adverse effect. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 35: e2772, 2019. 相似文献
143.
Linda M. Delahanty Thomas A. Wadden Pamela J. Goodwin Catherine M. Alfano Cynthia A. Thomson Melinda L. Irwin Marian L. Neuhouser Tracy E. Crane Elizabeth Frank Patricia A. Spears Bonnie P. Gillis Dawn L. Hershman Electra D. Paskett Judith Hopkins Vanessa Bernstein Vered Stearns Julia White Clifford Hudis Eric P. Winer Lisa A. Carey Ann H. Partridge Jennifer A. Ligibel 《Obesity (Silver Spring, Md.)》2022,30(1):28-38
144.
Cynthia C. Gonzalez Maria A. Gandolfo Maria C. Zamaloa Nestor R. Cúneo Peter Wilf Kirk R. Johnson 《The Botanical review》2007,73(3):235-266
Proteaceae are restricted to the Southern Hemisphere, and of the seven tribes of the subfamily Grevilleoideae, only three (Macadamieae, Oriteae, and Embothrieae) have living members in Argentina. Megafossil genera of Proteaceae recorded from Patagonia includeLomatia, Embothrium, Orites, andRoupala. In this report, we evaluate and revise fossil Argentine Proteaceae on the basis of type material and new specimens. The new collections come from the Tufolitas Laguna del Hunco (early Eocene, Chubut Province), the Ventana (middle Eocene, Río Negro Province), and the Río Ñirihuau (late Oligocene-early Miocene, Río Negro Province) formations, Patagonia, Argentina. We confirm the presence ofLomatia preferruginea Berry,L. occidentalis (Berry) Frenguelli,L. patagonica Frenguelli,Roupala patagonica Durango de Cabrera et Romero, andOrites bivascularis Romero, Dibbern et Gandolfo. Fossils assigned toEmbothrium precoccineum Berry andE. pregrandiflorum Berry are doubtful, and new material is necessary to confirm the presence of this genus in the fossil record of Patagonia. A putative new fossil species of Proteaceae is presented as Proteaceae gen. et sp. indet. Fossil Proteaceae are compared with modern genera, and an identification key for the fossil leaf species is presented. Doubtful historical records of Proteaceae fossils for the Antarctic Peninsula region and Patagonia are also discussed. Based on this revision, the three tribes of Proteaceae found today in Argentina were already present in Patagonia by the early Eocene, where they probably arrived via the Australia-Antarctica-South America connection. 相似文献
145.
146.
Considerable effort has been invested in determining traits underlying invasiveness. Yet, identifying a set of traits that
commonly confers invasiveness in a range of species has proven elusive, and almost nothing is known about genetic loci affecting
invasive success. Incorporating genetic model organisms into ecologically relevant studies is one promising avenue to begin
dissecting the genetic underpinnings of invasiveness. Molecular biologists are rapidly characterizing genes mediating developmental
responses to diverse environmental cues, i.e., genes for plasticity, as well as to environmental factors likely to impose
strong selection on invading species, e.g., resistance to herbivores and competitors, coordination of life-history events
with seasonal changes, and physiological tolerance of heat, drought, or cold. Here, we give an overview of molecular genetic
tools increasingly used to characterize the genetic basis of adaptation and that may be used to begin identifying genetic
mechanisms of invasiveness. Given the divergent traits that affect invasiveness, “invasiveness genes” common to many clades
are unlikely, but the combination of developmental genetic advances with further evolutionary studies and modeling may provide
a framework for identifying genes that account for invasiveness in related species. 相似文献
147.
Identifying the membrane proteome of HIV-1 latently infected cells 总被引:11,自引:0,他引:11
Berro R de la Fuente C Klase Z Kehn K Parvin L Pumfery A Agbottah E Vertes A Nekhai S Kashanchi F 《The Journal of biological chemistry》2007,282(11):8207-8218
Profiling integral plasma membrane proteins is of particular importance for the identification of new biomarkers for diagnosis and for drug development. We report in this study the identification of surface markers by performing comparative proteomics of established human immunodeficiency virus-1 (HIV-1) latent cell models and parental cell lines. To this end we isolated integral membrane proteins using a biotin-directed affinity purification method. Isolated proteins were separated by two-dimensional gel electrophoresis and identified by matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF) after in gel digestion. Seventeen different proteins were found to vary on the surface of T-cells due to HIV-1 infection. Of these proteins, 47% were integral membrane proteins, and 18% were membrane-associated. Through the use of complementary techniques such as Western blotting and fluorescent staining, we confirmed the differential expression of some of the proteins identified by MALDI-TOF including Bruton's tyrosine kinase and X-linked inhibitor of apoptosis. Finally, using phosphatidylinositol 3-kinase inhibitors and flavopiridol to inhibit Bruton's tyrosine kinase localization at the membrane and X-linked inhibitor of apoptosis protein expression, respectively, we showed that HIV-1 latently infected cells are more sensitive to these drugs than uninfected cells. This suggests that HIV-1 latently infected cells may be targeted with drugs that alter several pathways that are essential for the establishment and maintenance of latency. 相似文献
148.
Morris-Kukoski CL Jagerdeo E Schaff JE LeBeau MA 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2007,850(1-2):230-235
Detection, identification, and quantitation of ethanol and other low molecular weight volatile compounds in liquid matrices by headspace gas chromatography-flame ionization detection (HS-GC-FID) and headspace gas chromatography-mass spectrometry (HS-GC-MS) are becoming commonly used practices in forensic laboratories. Although it is one of the most frequently utilized procedures, sample preparation is usually done manually. Implementing the use of a dual-rail, programmable autosampler can minimize many of the manual steps in sample preparation. The autosampler is configured so that one rail is used for sample preparation and the other rail is used as a traditional autosampler for sample introduction into the gas chromatograph inlet. The sample preparation rail draws up and sequentially adds a saturated sodium chloride solution and internal standard (0.08%, w/v acetonitrile) to a headspace vial containing a biological sample, a calibrator, or a control. Then, the analytical rail moves the sample to the agitator for incubation, followed by sampling of the headspace for analysis. Using DB-624 capillary columns, the method was validated on a GC-FID and confirmed with a GC-MS. The analytes (ethanol, acetonitrile) and possible interferences (acetaldehyde, methanol, pentane, diethyl ether, acetone, isopropanol, methylene chloride, n-propanol, and isovaleraldehyde) were baseline resolved for both the GC-FID and GC-MS methods. This method demonstrated acceptable linearity from 0 to 1500 mg/dL. The lower limit of quantitation (LOQ) was determined to be 17 mg/dL and the limit of detection was 5 mg/dL. 相似文献
149.
Eberle MA Ng PC Kuhn K Zhou L Peiffer DA Galver L Viaud-Martinez KA Lawley CT Gunderson KL Shen R Murray SS 《PLoS genetics》2007,3(10):1827-1837
Advances in high-throughput genotyping and the International HapMap Project have enabled association studies at the whole-genome level. We have constructed whole-genome genotyping panels of over 550,000 (HumanHap550) and 650,000 (HumanHap650Y) SNP loci by choosing tag SNPs from all populations genotyped by the International HapMap Project. These panels also contain additional SNP content in regions that have historically been overrepresented in diseases, such as nonsynonymous sites, the MHC region, copy number variant regions and mitochondrial DNA. We estimate that the tag SNP loci in these panels cover the majority of all common variation in the genome as measured by coverage of both all common HapMap SNPs and an independent set of SNPs derived from complete resequencing of genes obtained from SeattleSNPs. We also estimate that, given a sample size of 1,000 cases and 1,000 controls, these panels have the power to detect single disease loci of moderate risk (λ ~ 1.8–2.0). Relative risks as low as λ ~ 1.1–1.3 can be detected using 10,000 cases and 10,000 controls depending on the sample population and disease model. If multiple loci are involved, the power increases significantly to detect at least one locus such that relative risks 20%–35% lower can be detected with 80% power if between two and four independent loci are involved. Although our SNP selection was based on HapMap data, which is a subset of all common SNPs, these panels effectively capture the majority of all common variation and provide high power to detect risk alleles that are not represented in the HapMap data. 相似文献
150.
Batchelder CA Bertolini M Mason JB Moyer AL Hoffert KA Petkov SG Famula TR Angelos J George LW Anderson GB 《Cloning and stem cells》2007,9(1):83-96
Although a majority of clones are born normal and apparently healthy, mortality rates of nearly 30% are described in many reports. Such losses are a major limitation of cloning technology and represent substantial economic investment as well as justifiable animal health and welfare concerns. Prospective, controlled studies are needed to understand fully the causes of neonatal mortality in clones and to develop preventive and therapeutic strategies to minimize losses. We report here the findings of studies on the hematologic and biochemical profiles of cloned and control calves in the immediate 48-h postpartum period. Cloned calves were similar to control calves for a majority of parameters studied including blood gases, concentrations of plasma proteins, minerals and electrolytes, and white blood cell, neutrophil, lymphocyte, and platelet counts. The most notable differences between clones and controls in this study were reduced red- and white-blood cell counts in clones at birth and 1 h of age. As a group, plasma electrolyte concentrations were more variable in clones, and the variability tended to be shifted either higher (sodium, chloride) or lower (potassium, bicarbonate) than in controls. Previously, we noted differences in carbohydrate parameters, the length of time required for clones to make the neonatal adaptation to life ex utero, and morphology of the cloned placenta. Taken together, our findings suggest that cloned calves experience greater difficulty adjusting to life ex utero and that further research is warranted to determine the nature of the relationship between the physiological differences noted here in clones at birth and concomitant abnormal placental morphology. 相似文献