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 Date : 2021/07/19 No:266 
 
 
 

Recent News

 
 
 
 
New Books
 
 
Period: 2021-07-19 ~ 2021-07-26
 
 
 
 
 
 

Database Introduction

 
 
 
 
HSTalks new releases

 
 
This Month's Releases of HSTalks the Biomedical & Life Sciences Collection
 
 
 
 
 
 
 
Database Trial

 
 
Please grasp the trial period of Wiley Digital Textbooks, which expires on 7/31/2021
 
 
 
 
 
 

Video Service

 
 
 
 
Welcome to browse the video of Health Talk

 
 
Title: 「Boost Immunity, Eat Healthy」: Application
Speakrer: Dr. Pan, Wen-Harn, IBMS
 
 
 
 
 
 
 
Video of Academic Ethics Workshop for Researcher by MOST

 
 
Title: Plagiarism and self plagiarism
Speaker: Dr. Sun, Y. Henry, IMB
 
 
 
 
 
 
 
Welcome to browse the video service of LSL courses

 
 
4/14 IPA Hands on Case Study (in Chinese)

4/22 Introduction to RNA-seq data Analysis(In English)
 
 
 
 
 
 

Blog

 
 
 
 
Scientific Laboratory Protocol and Method Resources

 
 
LSL provides links to online resources of laboratory protocols and methods that are used primarily in the life sciences.
 
 
 
 
 
 

Lectures

 
 
 
 
7/26 IBMS Seminar

 
 
Topic:The role of Akt-CBAP-TSC2-Rheb signalosome in growth factor signaling—Part II
Speaker:Dr. Yen, Jeffrey J.Y.
Date:07/26 (MON) 11:00 - 12:00
Place:Webex only
 
 
 
 
 
 
 
7/30 IPMB Sebinar

 
 
Topic:Type 2C Protein phosphatases and their target proteins that regulate growth during drought stress
Speaker:Dr. Paul Verslues
Time:2021-07-30 11:00
Place:presented virtually or physically depends on CECC's announcement
 
 
 
 
 
 

Important Research

 
 
 
 
Improvements of the productivity and saccharification efficiency of the cellulolytic β-glucosidase D2-BGL in Pichia pastoris via directed evolution

 
 
β-Glucosidases are essential for cellulose hydrolysis by catalyzing the final cellulolytic degradation of cello-oligomers and cellobiose to glucose. Dr. Tuan-Hua David Ho and his research team have discovered that the β-glucosidase D2-BGL, isolated from the fungus Chaetomella raphigera, has high substrate affinity and is an efficient β-glucosidase supplement to Trichoderma reesei cellulase mixtures for the saccharification of lignocellulosic biomass (Kao et al. 2019 Biotechnology for Biofuels).
 
 
 
 
 
 
 
 
Identification of MaWRKY40 and MaDLO1 as effective marker genes for tracking the salicylic acid-mediated immune response in bananas

 
 
Bananas lie among the world’s most important cash and staple crops but are threatened by various devastating pathogens. The phytohormone salicylic acid (SA) plays a key role in the regulation of plant immune response. Tracking the expression of SA-responsive marker genes under pathogen infection is important in pathogenesis elucidation. However, the common SA-responsive marker genes are not consistently induced in different banana cultivars or different organs. Here, we conducted transcriptome analysis for SA response of a banana cultivar, ‘Pei-Chiao’ (Cavendish, AAA genome), and identified three genes, MaWRKY40, MaWRKY70, and Downy Mildew Resistant 6 (DMR6)-Like Oxygenase 1 (MaDLO1) that are robustly induced upon SA treatment in both the leaves and roots.
 
 
 
 
 
 
 
A GalNAc/Gal-specific lectin modulates immune responses via toll-like receptor 4 independently of carbohydrate-binding ability

 
 
Toll-like receptor 4 (TLR4) recognizes various protein ligands; however, the protein-TLR4 binding model is unclear. Here we demonstrate a Crenomytilus grayanus lectin (CGL)-TLR4/MD2 model to show that CGL interacts with a TLR4/myeloid differentiation factor 2 (MD2) complex independently of sugar-binding properties. CGL could suppress lipopolysaccharide-induced immune responses significantly, suggesting that TLR4 itself has potential as a therapeutic target.
 
 
 
 
 
 
 
Differential effects of SUMO1 and SUMO2 on circadian protein PER2 stability and function

 
 
Posttranslational modification (PTM) of core circadian clock proteins, including Period2 (PER2), is required for proper circadian regulation. PER2 function is regulated by casein kinase 1 (CK1)-mediated phosphorylation and ubiquitination but little is known about other PER2 PTMs or their interaction with PER2 phosphorylation. We found that PER2 can be SUMOylated by both SUMO1 and SUMO2; however, SUMO1 versus SUMO2 conjugation had different effects on PER2 turnover and transcriptional suppressor function. SUMO2 conjugation facilitated PER2 interaction with β-TrCP leading to PER2 proteasomal degradation. In contrast, SUMO1 conjugation, mediated by E3 SUMO-protein ligase RanBP2, enhanced CK1-mediated PER2 S662 phosphorylation, inhibited PER2 degradation and increased PER2 transcriptional suppressor function. PER2 K736 was critical for both SUMO1- and SUMO2-conjugation. A PER2 K736R mutation was sufficient to alter PER2 protein oscillation and reduce PER2-mediated transcriptional suppression. Together, our data revealed that SUMO1 versus SUMO2 conjugation acts as a determinant of PER2 stability and function and thereby affects the circadian regulatory system and the expression of clock-controlled genes.
 
 
 
 
 
 
 
Genetically encoded multivalent liquid glycan array displayed on M13 bacteriophage

 
 
The central dogma of biology does not allow for the study of glycans using DNA sequencing. We report a liquid glycan array (LiGA) platform comprising a library of DNA 'barcoded' M13 virions that display 30-1,500 copies of glycans per phage. A LiGA is synthesized by acylation of the phage pVIII protein with a dibenzocyclooctyne, followed by ligation of azido-modified glycans. Pulldown of the LiGA with lectins followed by deep sequencing of the barcodes in the bound phage decodes the optimal structure and density of the recognized glycans. The LiGA is target agnostic and can measure the glycan-binding profile of lectins, such as CD22, on cells in vitro and immune cells in a live mouse. From a mixture of multivalent glycan probes, LiGAs identify the glycoconjugates with optimal avidity necessary for binding to lectins on living cells in vitro and in vivo.
 
 
 
 
 
 
 
TIFA protein expression is associated with pulmonary arterial hypertension

 
 
Tumor necrosis factor receptor-associated factor-interacting protein with a forkhead-associated domain (TIFA), a key regulator of inflammation, may be involved in the pathogenesis of pulmonary arterial hypertension (PAH). A total of 48 PAH patients (age 50.1 ± 13.1 years, 22.9% men), 25 hypertensive subjects, and 26 healthy controls were enrolled. TIFA protein expression in peripheral blood mononuclear cells (PBMCs) and plasma interleukin (IL)-1β and tumor necrosis factor (TNF)-α were measured. Pulmonary arterial hemodynamics were derived from right heart catheterization. PAH patients had the highest expression of TIFA, TNF-α, and IL-1β. TIFA protein expression was significantly associated with IL-1β (r = 0.94; P < 0.001), TNF-α (r = 0.93; P < 0.001), mean pulmonary artery pressure (r = 0.41; P = 0.006), and pulmonary vascular resistance (r = 0.41; P = 0.007). TIFA protein expression could independently predict the presence of PAH (odds ratio [95% confidence interval per-0.1 standard deviation]: 1.72 [1.37-2.16]; P < 0.001) and outperformed echocardiographic estimation. Ex vivo silencing of TIFA protein expression in PBMCs led to the suppression of the cellular expression of IL-1β and TNF-α. IL-1β and TNF-α mediated 80.4% and 56.6% of the causal relationship between TIFA and PAH, respectively, supporting the idea that TIFA protein is involved in the pathogenesis of PAH.
 
 
 
 
 
 
 
 
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