DOCSLIB.ORG

PDF (Dataset S01)

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
PDF (Dataset S01) Dataset S1 Effects of proteasome inhibition and deletion of Bag domain on association of proteins with Bag3 Full Length DeltaC Full Length BAG3 + BAG3 + Proteins BAG3 MG MG BAG family molecular chaperone regulator 3 OS=Homo sapiens GN=BAG3 PE=1 SV=3 BAG3_HUMAN Chaperone Heat shock cognate 71 kDa protein OS=Homo sapiens GN=HSPA8 PE=1 SV=1 HSP7C_HUMAN Chaperone 1.0000 0.4664 0.1197 Non-POU domain-containing octamer-binding protein OS=Homo sapiens GN=NONO PE=1 SV=4 NONO_HUMAN 1.0000 1.4531 2.2689 Heat shock 70 kDa protein 1A/1B OS=Homo sapiens GN=HSPA1A PE=1 SV=5 HSP71_HUMAN Chaperone 1.0000 0.3953 0.0917 Actin cytoplasmic 2 OS=Homo sapiens GN=ACTG1 PE=1 SV=1 ACTG_HUMAN Cytoskeleton 1.0000 0.0999 1.0625 Actin cytoplasmic 1 OS=Homo sapiens GN=ACTB PE=1 SV=1 ACTB_HUMAN Cytoskeleton 1.0000 0.3875 0.6755 Splicing factor proline- and glutamine-rich OS=Homo sapiens GN=SFPQ PE=1 SV=2 SFPQ_HUMAN 1.0000 1.7130 1.1645 Pyruvate kinase PKM OS=Homo sapiens GN=PKM PE=1 SV=4 KPYM_HUMAN 1.0000 0.1069 0.5828 Elongation factor 2 OS=Homo sapiens GN=EEF2 PE=1 SV=4 EF2_HUMAN 1.0000 0.5441 0.5029 78 kDa glucose-regulated protein OS=Homo sapiens GN=HSPA5 PE=1 SV=2 GRP78_HUMAN Chaperone 1.0000 0.8638 0.6490 Tubulin beta chain OS=Homo sapiens GN=TUBB PE=1 SV=2 TBB5_HUMAN Cytoskeleton 1.0000 0.0978 0.6262 Erythrocyte band 7 integral membrane protein OS=Homo sapiens GN=STOM PE=1 SV=3 STOM_HUMAN 1.0000 1.2862 1.1878 Heat shock protein HSP 90-beta OS=Homo sapiens GN=HSP90AB1 PE=1 SV=4 HS90B_HUMAN Chaperone 1.0000 0.6000 0.6635 Alpha-enolase OS=Homo sapiens GN=ENO1 PE=1 SV=2 ENOA_HUMAN 1.0000 0.7151 1.0212 Elongation factor 1-alpha 1 OS=Homo sapiens GN=EEF1A1 PE=1 SV=1 EF1A1_HUMAN Chaperone 1.0000 0.0745 0.5675 Peroxiredoxin-1 OS=Homo sapiens GN=PRDX1 PE=1 SV=1 PRDX1_HUMAN 1.0000 0.3115 0.1408 Tubulin alpha-1C chain OS=Homo sapiens GN=TUBA1C PE=1 SV=1 TBA1C_HUMAN Cytoskeleton 1.0000 0.0000 0.4706 Heat shock protein beta-1 OS=Homo sapiens GN=HSPB1 PE=1 SV=2 HSPB1_HUMAN Chaperone 1.0000 0.2781 0.9153 Filamin-A OS=Homo sapiens GN=FLNA PE=1 SV=4 FLNA_HUMAN Cytoskeleton 1.0000 0.5938 0.3081 Polypeptide N-acetylgalactosaminyltransferase 2 OS=Homo sapiens GN=GALNT2 PE=1 SV=1 GALT2_HUMAN 1.0000 0.7273 0.8656 Signaling Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 FAS_HUMAN factor 1.0000 0.6576 0.6377 Peptidyl-prolyl cis-trans isomerase A OS=Homo sapiens GN=PPIA PE=1 SV=2 PPIA_HUMAN Chaperone 1.0000 0.3311 0.2079 T-complex protein 1 subunit eta OS=Homo sapiens GN=CCT7 PE=1 SV=2 TCPH_HUMAN Chaperone 1.0000 0.3984 0.6412 Fructose-bisphosphate aldolase A OS=Homo sapiens GN=ALDOA PE=1 SV=2 ALDOA_HUMAN 1.0000 0.1459 0.5689 Tubulin alpha-4A chain OS=Homo sapiens GN=TUBA4A PE=1 SV=1 TBA4A_HUMAN Cytoskeleton 1.0000 0.0000 0.5413 T-complex protein 1 subunit gamma OS=Homo sapiens GN=CCT3 PE=1 SV=4 TCPG_HUMAN Chaperone 1.0000 0.4057 0.5679 Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Homo sapiens GN=DHX15 PE=1 SV=2 DHX15_HUMAN 1.0000 1.7784 2.3078 ATP-citrate synthase OS=Homo sapiens GN=ACLY PE=1 SV=3 ACLY_HUMAN 1.0000 0.8348 0.6814 Glyceraldehyde-3-phosphate dehydrogenase OS=Homo sapiens GN=GAPDH PE=1 SV=3 G3P_HUMAN 1.0000 0.1115 0.3549 T-complex protein 1 subunit delta OS=Homo sapiens GN=CCT4 PE=1 SV=4 TCPD_HUMAN Chaperone 1.0000 0.4871 0.4782 Zinc transporter 1 OS=Homo sapiens GN=SLC30A1 PE=1 SV=3 ZNT1_HUMAN 1.0000 0.6117 0.9919 Signaling Annexin A2 OS=Homo sapiens GN=ANXA2 PE=1 SV=2 ANXA2_HUMAN factor 1.0000 0.6616 0.2696 T-complex protein 1 subunit beta OS=Homo sapiens GN=CCT2 PE=1 SV=4 TCPB_HUMAN Chaperone 1.0000 0.3762 0.6676 Heat shock protein HSP 90-alpha OS=Homo sapiens GN=HSP90AA1 PE=1 SV=5 HS90A_HUMAN Chaperone 1.0000 0.5468 0.6360 Granulins OS=Homo sapiens GN=GRN PE=1 SV=2 GRN_HUMAN 1.0000 1.7027 1.0674 Poly(rC)-binding protein 1 OS=Homo sapiens GN=PCBP1 PE=1 SV=2 PCBP1_HUMAN 1.0000 0.6749 0.8201 www.pnas.org/cgi/doi/10.1073/pnas.1803130115 60 kDa heat shock protein mitochondrial OS=Homo sapiens GN=HSPD1 PE=1 SV=2 CH60_HUMAN 1.0000 0.2085 0.6890 Signaling Epidermal growth factor receptor OS=Homo sapiens GN=EGFR PE=1 SV=2 EGFR_HUMAN factor 1.0000 1.2282 1.4705 Multifunctional protein ADE2 OS=Homo sapiens GN=PAICS PE=1 SV=3 PUR6_HUMAN 1.0000 0.7524 0.6634 DNA topoisomerase 1 OS=Homo sapiens GN=TOP1 PE=1 SV=2 TOP1_HUMAN 1.0000 1.2734 1.8084 Signaling Ezrin OS=Homo sapiens GN=EZR PE=1 SV=4 EZRI_HUMAN factor 1.0000 1.0663 0.6927 Phosphoglycerate kinase 1 OS=Homo sapiens GN=PGK1 PE=1 SV=3 PGK1_HUMAN 1.0000 0.2756 0.4271 T-complex protein 1 subunit epsilon OS=Homo sapiens GN=CCT5 PE=1 SV=1 TCPE_HUMAN Chaperone 1.0000 0.6582 0.2986 LIM and SH3 domain protein 1 OS=Homo sapiens GN=LASP1 PE=1 SV=2 LASP1_HUMAN Cytoskeleton 1.0000 0.6821 0.4911 Stress-induced-phosphoprotein 1 OS=Homo sapiens GN=STIP1 PE=1 SV=1 STIP1_HUMAN Chaperone 1.0000 0.7210 0.2436 ATP-dependent RNA helicase DDX42 OS=Homo sapiens GN=DDX42 PE=1 SV=1 DDX42_HUMAN 1.0000 0.6004 0.8034 T-complex protein 1 subunit theta OS=Homo sapiens GN=CCT8 PE=1 SV=4 TCPQ_HUMAN Chaperone 1.0000 0.6258 0.7152 Transcriptional repressor protein YY1 OS=Homo sapiens GN=YY1 PE=1 SV=2 TYY1_HUMAN 1.0000 0.7863 0.8012 Cofilin-1 OS=Homo sapiens GN=CFL1 PE=1 SV=3 COF1_HUMAN Cytoskeleton 1.0000 0.5098 0.8934 Eukaryotic translation initiation factor 5A-1 OS=Homo sapiens GN=EIF5A PE=1 SV=2 IF5A1_HUMAN 1.0000 0.2174 0.5094 Zinc transporter ZIP10 OS=Homo sapiens GN=SLC39A10 PE=1 SV=2 S39AA_HUMAN 1.0000 1.3921 0.8672 Signaling 14-3-3 protein zeta/delta OS=Homo sapiens GN=YWHAZ PE=1 SV=1 1433Z_HUMAN factor 1.0000 1.7280 0.0000 Protein disulfide-isomerase A3 OS=Homo sapiens GN=PDIA3 PE=1 SV=4 PDIA3_HUMAN Chaperone 1.0000 0.5623 0.8861 Peroxiredoxin-4 OS=Homo sapiens GN=PRDX4 PE=1 SV=1 PRDX4_HUMAN 1.0000 0.9211 0.7464 D-3-phosphoglycerate dehydrogenase OS=Homo sapiens GN=PHGDH PE=1 SV=4 SERA_HUMAN Chaperone 1.0000 0.7443 0.2308 Alpha-actinin-4 OS=Homo sapiens GN=ACTN4 PE=1 SV=2 ACTN4_HUMAN Cytoskeleton 1.0000 0.3823 0.4333 Ubiquitin-60S ribosomal protein L40 OS=Homo sapiens GN=UBA52 PE=1 SV=2 RL40_HUMAN 1.0000 2.8518 1.5032 T-complex protein 1 subunit zeta OS=Homo sapiens GN=CCT6A PE=1 SV=3 TCPZ_HUMAN Chaperone 1.0000 0.4986 0.2180 Signaling 14-3-3 protein beta/alpha OS=Homo sapiens GN=YWHAB PE=1 SV=3 1433B_HUMAN factor 1.0000 1.3300 0.8016 Pleckstrin homology-like domain family A member 1 OS=Homo sapiens Signaling GN=PHLDA1 PE=1 SV=4 PHLA1_HUMAN factor 1.0000 1.0475 0.3494 Elongation factor Tu mitochondrial OS=Homo sapiens GN=TUFM PE=1 SV=2 EFTU_HUMAN 1.0000 0.7367 0.3485 Serum albumin OS=Homo sapiens GN=ALB PE=1 SV=2 ALBU_HUMAN 1.0000 1.0342 0.5854 Signaling 14-3-3 protein gamma OS=Homo sapiens GN=YWHAG PE=1 SV=2 1433G_HUMAN factor 1.0000 1.2109 0.9017 Eukaryotic initiation factor 4A-I OS=Homo sapiens GN=EIF4A1 PE=1 SV=1 IF4A1_HUMAN 1.0000 0.6714 0.1160 ATP synthase subunit beta mitochondrial OS=Homo sapiens GN=ATP5B PE=1 SV=3 ATPB_HUMAN 1.0000 0.1462 0.5469 Transitional endoplasmic reticulum ATPase OS=Homo sapiens GN=VCP PE=1 Signaling SV=4 TERA_HUMAN factor 1.0000 0.4483 0.4224 ATP synthase subunit alpha mitochondrial OS=Homo sapiens GN=ATP5A1 PE=1 SV=1 ATPA_HUMAN 1.0000 0.3860 0.6225 Testin OS=Homo sapiens GN=TES PE=1 SV=1 TES_HUMAN 1.0000 0.8547 0.4226 Signaling Coatomer subunit alpha OS=Homo sapiens GN=COPA PE=1 SV=2 COPA_HUMAN factor 1.0000 0.3876 0.2336 Peroxiredoxin-2 OS=Homo sapiens GN=PRDX2 PE=1 SV=5 PRDX2_HUMAN 1.0000 0.5131 0.1684 Heat shock protein beta-8 OS=Homo sapiens GN=HSPB8 PE=1 SV=1 HSPB8_HUMAN Chaperone 1.0000 1.0031 0.9252 L-lactate dehydrogenase B chain OS=Homo sapiens GN=LDHB PE=1 SV=2 LDHB_HUMAN 1.0000 0.9582 0.9447 Signaling WD repeat-containing protein 1 OS=Homo sapiens GN=WDR1 PE=1 SV=4 WDR1_HUMAN factor 1.0000 0.5805 0.2870 Profilin-1 OS=Homo sapiens GN=PFN1 PE=1 SV=2 PROF1_HUMAN Cytoskeleton 1.0000 0.3641 0.7875 L-lactate dehydrogenase A chain OS=Homo sapiens GN=LDHA PE=1 SV=2 LDHA_HUMAN 1.0000 0.6627 0.6650 Transketolase OS=Homo sapiens GN=TKT PE=1 SV=3 TKT_HUMAN 1.0000 0.6148 0.6042 Inosine-5'-monophosphate dehydrogenase 2 OS=Homo sapiens GN=IMPDH2 PE=1 SV=2 IMDH2_HUMAN 1.0000 0.6024 0.0000 Vinculin OS=Homo sapiens GN=VCL PE=1 SV=4 VINC_HUMAN Cytoskeleton 1.0000 0.4515 0.4447 Eukaryotic translation initiation factor 2 subunit 3 OS=Homo sapiens GN=EIF2S3 PE=1 SV=3 IF2G_HUMAN 1.0000 0.6862 0.6477 Heterogeneous nuclear ribonucleoprotein L OS=Homo sapiens GN=HNRNPL PE=1 SV=2 HNRPL_HUMAN 1.0000 2.5729 2.1460 Threonine--tRNA ligase cytoplasmic OS=Homo sapiens GN=TARS PE=1 SV=3 SYTC_HUMAN 1.0000 0.0000 0.4872 Stress-70 protein mitochondrial OS=Homo sapiens GN=HSPA9 PE=1 SV=2 GRP75_HUMAN Chaperone 1.0000 1.0541 0.6863 Glutathione S-transferase P OS=Homo sapiens GN=GSTP1 PE=1 SV=2 GSTP1_HUMAN 1.0000 0.3250 0.6600 Putative nucleoside diphosphate kinase OS=Homo sapiens GN=NME2P1 PE=5 SV=1 NDK8_HUMAN 1.0000 0.6464 0.4020 Signaling Cytoskeleton-associated protein 4 OS=Homo sapiens GN=CKAP4 PE=1 SV=2 CKAP4_HUMAN factor 1.0000 0.8313 2.3207 Activated RNA polymerase II transcriptional coactivator p15 OS=Homo sapiens GN=SUB1 PE=1 SV=3 TCP4_HUMAN Chaperone 1.0000 0.8486 0.4508 Splicing factor 3B subunit 2 OS=Homo sapiens GN=SF3B2 PE=1 SV=2 SF3B2_HUMAN 1.0000 1.4806 0.3532 Fascin OS=Homo sapiens GN=FSCN1 PE=1 SV=3 FSCN1_HUMAN Cytoskeleton 1.0000 0.6730 0.5491 Signaling Nucleophosmin OS=Homo sapiens GN=NPM1 PE=1 SV=2 NPM_HUMAN factor 1.0000 0.0027 1.0522 Prohibitin OS=Homo sapiens GN=PHB PE=1 SV=1 PHB_HUMAN 1.0000 0.2221 1.8892 C-1-tetrahydrofolate synthase cytoplasmic OS=Homo sapiens GN=MTHFD1 PE=1 SV=3 C1TC_HUMAN 1.0000 0.7847 0.0000 Elongation factor 1-delta OS=Homo sapiens GN=EEF1D PE=1
Load more

Recommended publications
  • List & Label Preview File
    L I N A R I S I n f o r m a t i o n B I O L O G I S C H E P R O D U K T E PRIMÄRANTIKÖRPER-Veterinär erkennen: Maus, verschiedene Labels alphabetisch geordnet Beschreibung Format Klon Wirt Isotyp Anwendung Menge ME Kat.Nr. Description Format Clone Host Isotype Application Quantity Cat.No. Mouse Anti-Cardiolipin Ig's -ve control for ELISA 1 ml ADI-5502 IgG Mouse 0,5 mg ADI-AMPT11-M-500 Anti-Cardiolipin Ig's +ve control for ELISA polyclonal Mouse 1 ml ADI-5503 CD27 PE (Armenian Hamster IgG1) Hamster 50 tests ADI-MCD027-PE Monoclonal Anti-VSV-G-Cy conjugate for Mouse 0,1 mg ADI-VSV11-Cy Immunofluorescence Interleukin-4 IgG Mouse 0,1 mg ADI-AB-10710 Anti-Myelin Oligodendrocyte Glycoprotein IgG Mouse 0,1 mg ADI-AB-19910 CD160 mAb, PE, , (mouse IgG2bk) Mouse 50 tests ADI-MCD160-PE CD81, Purified (mouse IgG1) Mouse 0,1 mg ADI-MCD081-UL Interleukin-2 receptor IgG Rat 0,1 mg ADI-AB-10310 Interleukin-2 IgG Rat 0,1 mg ADI-AB-10510 Interleukin-4 IgG Rat 0,1 mg ADI-AB-10810 Interleukin-10 IgG Rat 0,1 mg ADI-AB-11310 Interleukin-12p40 IgG Rat 0,1 mg ADI-AB-11410 CTLA-4 IgG Rat 0,1 mg ADI-AB-11610 CD80 IgG Rat 0,1 mg ADI-AB-13310 CD11a IgG Rat 0,1 mg ADI-AB-13510 CD11b-FITC IgG Rat 0,1 mg ADI-AB-13610 B220 IgG Rat 0,1 mg ADI-AB-13910 CD90 Thy-1.1 IgG Rat 0,1 mg ADI-AB-14010 CD90 Thy-1.2 IgG Rat 0,1 mg ADI-AB-14110 CD90 Thy-1 IgG Rat 0,1 mg ADI-AB-14210 CD4 IgG Rat 0,1 mg ADI-AB-16510 IFN-gamma IgG Rat 0,1 mg ADI-AB-16610 CD3 IgG Rat 0,1 mg ADI-AB-17510 Interleukin-12p75 IgG Rat 0,1 mg ADI-AB-20910 CD8b , PE-Cy5 (Clone CT-CD8b) (rat IgG2a) Rat 50 tests
    [Show full text]
  • Monoacylglycerol As a Metabolic Coupling Factor in Glucose-Stimulated Insulin Secretion
    Université de Montréal Monoacylglycerol as a metabolic coupling factor in glucose-stimulated insulin secretion par Shangang Zhao Département de Biochimie Faculté de Médecine Mémoire présentée à la Faculté des Etudes Supérieures en vue de l’obtention du grade de maître ès sciences en Biochimie Décembre 2010 © Shangang Zhao, 2010 Université de Montréal Faculté des études supérieures Ce mémoire intitulée : Monoacylglycerol as a metabolic coupling factor in glucose-stimulated insulin secretion Présenté par : Shangang Zhao a été évaluée par un jury composé des personnes suivantes: Dr Tony Antakly, président-rapporteur Dr Marc Prentki, directeur de recherche Dr Ashok K. Srivastava, membre du jury i Résumé Les cellules beta pancréatiques sécrètent l’insuline lors d’une augmentation post-prandiale du glucose dans le sang. Ce processus essentiel est contrôlé par des facteurs physiologiques, nutritionnels et pathologiques. D’autres sources d’énergie, comme les acides aminés (leucine et glutamine) ou les acides gras potentialisent la sécrétion d’insuline. Une sécrétion d’insuline insuffisante au besoin du corps déclanche le diabète. Le rôle que joue l’augmentation du calcium intracellulaire et les canaux K+/ATP dans la sécrétion d’insuline est bien connu. Bien que le mécanisme exact de la potentialisation de la sécrétion d’insuline par les lipides est inconnu, le cycle Glycérolipides/Acides gras (GL/FFA) et son segment lipolytique ont été reconnu comme un composant essentiel de la potentialisation lipidique de la sécrétion d’insuline. Le diacylglycérol, provenant de la lipolyse, a été proposé comme un signal lipidique important d’amplification. Cependant, l’hydrolyse des triglycérides et des diacylglycérides a été démontrée essentielle pour la sécrétion d’insuline stimulée par le glucose, en suggérant un rôle du monoacylglycérol (MAG) dans ce processus.
    [Show full text]
  • Supplemental Data
    Article TCF7L2 is a master regulator of insulin production and processing ZHOU, Yuedan, et al. Abstract Genome-wide association studies have revealed >60 loci associated with type 2 diabetes (T2D), but the underlying causal variants and functional mechanisms remain largely elusive. Although variants in TCF7L2 confer the strongest risk of T2D among common variants by presumed effects on islet function, the molecular mechanisms are not yet well understood. Using RNA-sequencing, we have identified a TCF7L2-regulated transcriptional network responsible for its effect on insulin secretion in rodent and human pancreatic islets. ISL1 is a primary target of TCF7L2 and regulates proinsulin production and processing via MAFA, PDX1, NKX6.1, PCSK1, PCSK2 and SLC30A8, thereby providing evidence for a coordinated regulation of insulin production and processing. The risk T-allele of rs7903146 was associated with increased TCF7L2 expression, and decreased insulin content and secretion. Using gene expression profiles of 66 human pancreatic islets donors', we also show that the identified TCF7L2-ISL1 transcriptional network is regulated in a genotype-dependent manner. Taken together, these results demonstrate that not only synthesis of [...] Reference ZHOU, Yuedan, et al. TCF7L2 is a master regulator of insulin production and processing. Human Molecular Genetics, 2014, vol. 23, no. 24, p. 6419-6431 DOI : 10.1093/hmg/ddu359 PMID : 25015099 Available at: http://archive-ouverte.unige.ch/unige:45177 Disclaimer: layout of this document may differ from the published
    [Show full text]
  • ANALYSIS of GENE PATHWAYS INVOLVED in DCIS PROGRESSION in RESPONSE to ACIDIC EXTRACELLULAR Ph Neha Aggarwal1, Jennifer Rothberg2, Robert J
    ANALYSIS OF GENE PATHWAYS INVOLVED IN DCIS PROGRESSION IN RESPONSE TO ACIDIC EXTRACELLULAR pH Neha Aggarwal1, Jennifer Rothberg2, Robert J. Gillies3 and Bonnie F. Sloane4 & Douglas Yingst 1Department of Physiology, 2Cancer Biology Program, and 4Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI, 48201; 3H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33602 Breast cancer is the most commonly diagnosed cancer in women in USA and has a high mortality rate, second only to lung cancer. About 85% of total 63300 new cases of breast cancer are predicted to be ductal carcinoma in situ (DCIS) in 2012. We are interested in identifying markers that are predictive of changes that occur in the breast microenvironment as a result of the presence of premalignant lesions such as DCIS that are poised to develop into breast cancer. A critical barrier to cancer progression is its ability to survive in the acidic microenvironment characteristic of breast cancer. As the breast is comprised of different cell types, we performed gene expression analysis using Affymetrix gene chip HG U133 plus 2.0 array of 3 DCIS cell lines grown in 3D at neutral and acidic pH. We then computed the significantly changed genes at acidic pH for three DCIS cell lines and found 6 common and 121 similar genes. IPA core analysis of these genes revealed the interferon-signaling (IFN) pathway to be significantly altered. STAT1 was one key transcription factor that was upregulated and that might be driving downstream signaling as a response to acidic microenvironment. We are validating some of the downstream targets of the IFN pathway using qPCR.
    [Show full text]
  • Alterations in the Intestinal Morphology, Gut Microbiota
    nutrients Article Alterations in the Intestinal Morphology, Gut Microbiota, and Trace Mineral Status Following Intra-Amniotic Administration (Gallus gallus) of Teff (Eragrostis tef) Seed Extracts Johnathon Carboni 1, Spenser Reed 2,3, Nikolai Kolba 2 , Adi Eshel 4, Omry Koren 4 and Elad Tako 2,* 1 Department of Biological Sciences, Cornell University, Ithaca, NY 14853, USA; [email protected] 2 Department of Food Science, Cornell University, Stocking Hall, Ithaca, NY 14853-7201, USA; [email protected] (S.R.); [email protected] (N.K.) 3 Department of Family Medicine, Kaiser Permanente Fontana Medical Centers, Fontana, CA 92335, USA 4 Azrieli Faculty of Medicine, Bar-Ilan University, 1311502 Safed, Israel; [email protected] (A.E.); [email protected] (O.K.) * Correspondence: [email protected]; Tel.: +1-607-255-0884 Received: 20 August 2020; Accepted: 30 September 2020; Published: 2 October 2020 Abstract: The consumption of teff (Eragrostis tef ), a gluten-free cereal grain, has increased due to its dense nutrient composition including complex carbohydrates, unsaturated fatty acids, trace minerals (especially Fe), and phytochemicals. This study utilized the clinically-validated Gallus gallus intra amniotic feeding model to assess the effects of intra-amniotic administration of teff extracts versus controls using seven groups: (1) non-injected; (2) 18W H2O injected; (3) 5% inulin; (4) teff extract 1%; (5) teff extract 2.5%; (6) teff extract 5%; and (7) teff extract 7.5%. The treatment groups were compared to each other and to controls. Our data demonstrated a significant improvement in hepatic iron (Fe) and zinc (Zn) concentration and LA:DGLA ratio without concomitant serum concentration changes, up-regulation of various Fe and Zn brush border membrane proteins, and beneficial morphological changes to duodenal villi and goblet cells.
    [Show full text]
  • Functional Characterisation of the Barley ZIP7 Zinc Transporter
    Functional characterisation of the barley ZIP7 zinc transporter Jingwen Tiong B. Science (Hons), The University of Adelaide A thesis submitted for the degree of Doctor of Philosophy The University of Adelaide Faculty of Sciences School of Agriculture, Food & Wine Waite Campus February 2012 I Contents List of figures ......................................................................................................................... VI List of tables ......................................................................................................................... VII Abstract ............................................................................................................................... VIII Declaration .............................................................................................................................. X Acknowledgements ............................................................................................................... XI Glossary of abbreviations .................................................................................................. XIII Chapter 1: Literature Review ................................................................................................. 1 1.1 Introduction ...................................................................................................................... 1 1.2 Improvement of plant Zn nutrition and biofortification .................................................. 3 1.2.1 Application of Zn fertilisers as an agronomic
    [Show full text]
  • Mirnas Documented to Play a Role in Hematopoietic Cell Lineage. Our
    Table S1: miRNAs documented to play a role in hematopoietic cell lineage. Our review of the literature summarizing miRNAs known to be involved in the development and proliferation of the hematopoietic lineage cells. miRNA Expression/function/target/regulator References miR-150 Elevated during developmental stages of B and T cell maturation. 16-19 Controls B cell differentiation, present in mature, resting T and B cells but decreased upon activation of naïve T or B cells. Plays a role in establishing lymphocyte identity. Very little is known about function in T cells. Regulators: Foxp3 Target: C-Myb miR-146a/b Upregulated in macropgahe inflammatory response. Differentially 17, 20 upregulated in murine Th1 subset but abolished in Th2 subset. Upregulated in response to TCRs stimulation, as well as by IL-1 and TNF. Highly expressed in murine T-regs and could play a role in establishing lymphocyte identity. Modulates activation induced cell death in activated T cells. Negative regulator of TLR and cytokine signaling pathway. Endotoxin tolerance. Antiviral role. Targets: IRAK1, IRAK2, TRAF6, FAF1 miR-16-1 Promote apoptosis by targeting Bcl2 expression, act as tumor 22 cluster suppressor RNAs. May block differentiation of later stage hematopoietic progenitor cells to mature cells. Downregulated in CLL. Target: BCL2. miR-155 Regulator of T and B cell maturation and innate immune response. 23-29 Expressed in primary mediastinal B-cell lymphoma, T and B cells, macrophages and DCs. Upregulated during B cell activation. Involved in T cell differentiation and indicated as a positive regulator of cytokine production. Activated by stimulating TLR3 and INFab receptors in bone derived macrophages (regulation of antimicrobial defense).
    [Show full text]
  • Genetic Variation of Traits Related to Salt Stress Response in Wheat (Triticum Aestivum L.)
    Institut für Nutzpflanzenwissenschaften und Ressourcenschutz Genetic variation of traits related to salt stress response in Wheat (Triticum aestivum L.) Dissertation zur Erlangung des Grades Doktor der Agrarwissenschaften (Dr. agr.) der Landwirtschaftlichen Fakultät der Rheinischen Friedrich-Wilhelms-Universität Bonn vorgelegt von Oyiga Benedict Chijioke aus Enugu-Ezike, Nigeria Bonn 2017 Referent: Prof. Dr. Jens Léon Plant Breeding, INRES, University of Bonn Korreferent: Prof. Dr. Heiner Goldbach Plant Nutrition, INRES, University of Bonn Tag der Mündlichen Prüfung: 14.12. 2016 This research work was financially supported by the “Bundesministerium fur wirtschaftliche Zusammenarbeit und Entwicklung (BMZ)” in collaboration with the German Agency for International Cooperation (GIZ), Germany (Project number: 09.7860.1-001.00), the International Centre for Research in Dryland Agriculture (ICARDA) and the Center for Development Research (ZEF), Friedrich-Wilhelms-University, Bonn, Germany. Angefertigt mit Genehmigung der Landwirtschaftlichen Fakultät der Universität Bonn ii GENERAL SUMMARY (English) Salinity is one of the most severe abiotic stresses perceived by plants, and is continuously increasing due to climatic change and poor irrigation management practices. It is currently affecting ~800 million hectares of land worldwide, including over 20% of the world’s irrigated arable land. Salinity causes significant growth reduction and crop yield losses. With the predicted geometric increase in the global population, improving the salt tolerance (ST) of crops has become an important challenge and target for plant breeders. Several approaches have been exhaustively exploited to ameliorate the impact of salinity on crop plants, but because of the complex nature of ST in crop plant, these approaches have not been optimally translated into the desired results.
    [Show full text]
  • Title Methods to Evaluate Zinc Transport Into and out of the Secretory and Endosomal-Lysosomal Compartments in DT40 Cells. Autho
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Kyoto University Research Information Repository Methods to Evaluate Zinc Transport into and out of the Title Secretory and Endosomal-Lysosomal Compartments in DT40 Cells. Author(s) Kambe, Taiho Citation Methods in enzymology (2014), 534: 77-92 Issue Date 2014 URL http://hdl.handle.net/2433/180109 Right © 2014 Elsevier Inc. Type Journal Article Textversion author Kyoto University Running title: Zinc transport in subcellular compartments Methods to evaluate zinc transport into and out of the secretory and endosomal-lysosomal compartments in DT40 cells Taiho Kambe Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan Email: [email protected] Tel: +81-75-753-6273 Keywords: zinc, ZIP (Zrt/Irt-like protein), ZnT (zinc transporter), signaling, secretory and endosomal-lysosomal compartments, DT40, multiple gene disruptions 1 Abstract Zinc plays crucial roles in diverse biological processes. Recently, in addition to zinc mobilization into and out of the cell, zinc mobilization into and out of intracellular organelles, including the secretory and endosomal-lysosomal compartments, has received growing interest. In vertebrate cells, the Zrt/Irt-like proteins (ZIPs) and zinc transporters (ZnTs) are the two major families of zinc transporters involved in zinc mobilization across cellular membranes. Importantly, nearly half of ZIP and ZnT transporters are localized to subcellular compartments. Thus, to elucidate the numerous zinc-related cellular events, understanding ZIP and ZnT functions is critical. This chapter describes advanced methods used in our laboratory to examine zinc mobilization. Specifically, genetic and molecular approaches using chicken DT40 cells deficient in multiple ZnT and ZIP transporters are described.
    [Show full text]
  • The Function of Zinc Transporters in Human Cells
    THE FUNCTION OF ZINC TRANSPORTERS IN HUMAN CELLS BY LOVELEEN KUMAR, BSc., MSc. Submitted in fulfilment of requirements for the degree of Doctor of Philosophy DEAKIN UNIVERSITY JULY 2014 i Acknowledgements I would sincerely like to thank my supervisor Professor Leigh Ackland for giving me the opportunity to undertake my PhD under her invaluable guidance with continual support, encouragement and infinite enthusiasm. Thank you so much Leigh for having faith in me and being wonderful supervisor one could ever wish for. I would like to thank my co-supervisor Dr Agnes Michalczyk, not only for providing invaluable supervision and encouragement but being a great friend who I could talk to during hard times. Thanks a lot Agnes for being always there to support me. I am grateful to Professor Julian Mercer for allowing me to undertake my PhD candidature in the CCMB. I would also like to thank him for his expert advice at the discussion sessions that made me think in detail. Special thanks to Prof Andy Sinclair for providing me the scholarship and the mentoring sessions we had, it made me concentrate on the main goal. I would like to thank my Lab Manager Mr. Michael Holmes for having faith in my capability and providing me with opportunity to work as a technical officer to financially support my family. I am very grateful to our school manager Marita Reynolds to sanction my study leave to finish off my writting. I would like to extend that thanks to all Technical staff, who gave enormous mental support and friendly environment that helped me come out of my grief.
    [Show full text]
  • Supporting Information
    Supporting Information Redefining the breast cancer exosome proteome by tandem mass tag quantitative proteomics and multivariate cluster analysis. David J Clarkǂ*1,2, William E Fondrieǂ2,3, Zhongping Liao4, Phyllis I Hanson5, Amy Fulton2, Li Mao1,2, Austin J Yang2 1 Department of Oncology and Diagnostic Sciences, University of Maryland School of Dentistry, Baltimore, MD 2 Marlene and Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, MD 3Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD 4 Lily Research Laboratory, Eli Lily and Company, Indianapolis, IN 5Department of Cell Biology and Physiology, Washington University, St. Louis, MO ǂ These authors contributed equally to this work. *Corresponding author: [email protected] 410-706-6114 Table of Contents Figure S-1: TMT log2 protein ratios were plotted by 100K enrichment against Optiprep/100K enrichment. (pg. S-2) Figure S-2: Immunoblot of SEC fractions, and Venn diagram of SEC and TMT-SVM analysis. (pg. S-3) Table S-1 Protein identifications, TMT ratios, SVM Classification and SVM Probability of 10K, 100K, and Optiprep lysates derived from SKBR3B conditioned media. (pg. S-4) Table S-2. Plasma membrane markers and their respective SVM Classification (pg. S-75) Table S-3. Identified proteins from our SEC analysis with respective Protein Prophet probability (pg. S-76) S-1 Figure S-1. Known exosome markers localize to quadrant corresponding to 100K enrichment. TMT log2 protein ratios were plotted by 100K enrichment (x-axis) against Optiprep/100K enrichment (y-axis). Selected Exosome (red) and Non-exosome (blue) protein markers are annotated.
    [Show full text]
  • Zinc Signaling in Physiology and Pathogenesis
    International Journal of Molecular Sciences Books Zinc Signaling in Physiology and Pathogenesis Edited by Toshiyuki Fukada and Taiho Kambe Printed Edition of the Special Issue Published in IJMS www.mdpi.com/journal/ijms MDPI Zinc Signaling in Physiology and Pathogenesis Special Issue Editors Toshiyuki Fukada Books Taiho Kambe MDPI • Basel • Beijing • Wuhan • Barcelona • Belgrade MDPI Special Issue Editors ToshiyukiFukada TokushimaBunri University Japan TaihoKambe Kyoto University Japan Editorial Office MDPI St. Alban-Anlage 66 Basel, Switzerland This edition is a reprint of the Special Issue published online in the open access journal IJMS (ISSN 1422-0067) from 2017-2018(available at: http:/ /www.mdpi.com/journal/ijms/special...issues/ zinc...signaling). Books For citation purposes, cite each article independently as indicated on the article page online and as indicated below: Lastname, F.M.; Lastname, F.M. Article title. Journal Name Year,A rticle number, page range. First Edition 2018 ISBN 978-3-03842-821-3 (Pbk) ISBN 978-3-03842-822-0 (PDF) Cover photo courtesy ofKoh-ei Toyoshimaand TakashiTsuji. It depicts mouse epidermal hair follicles which express zinc transporter ZIPlO (Bum-Ho Bin et al. PNAS 114, 12243-12248, 2017) Articles in this volume are Open Access and distributed under the Creative Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles even for commercial purposes, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. The book taken as a whole is©2018 MDPI, Basel, Switzerland, distributed under the terms and conditions of the Creative Commons license CC BY-NC-ND(http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
    [Show full text]