Using bioinformatic tools to examine similarities between human PDL-1 protein and common tobacco (Nicotiana tabacum).

2020 ◽  
Vol 38 (5_suppl) ◽  
pp. 70-70
Author(s):  
Elie G. Dib ◽  
Nicholas Hill ◽  
Jessica Wollard ◽  
Ji Woon Yoo ◽  
Joe E. Dib ◽  
...  

70 Background: Human CD274 receptor, known as programmed cell death 1 ligand 1 (RefSeq NP_054862.1), is an inhibitory ligand for Programmed cell death protein 1 (PD1). We aimed in this bioinformatic experiment to identify a homologous PDL-1 protein in plants. Methods: We chose to use tBLASTn because it compares a protein query sequence against a nucleotide sequence database dynamically translated in all six reading frames (both strands). We chose the EST database and restricted our search to plants (Viridiplantae). Results: Using the FASTA sequence of PDL-1 protein, the tBLASTn of the CD274 protein produced a single hit to Nicotiana tabacum (Common tobacco) cDNA, accession number FG181602.1 with E value of 2e-13 and score of 75.9. We translated the FASTA FG181602.1 through ExPASy and after inspecting the results of the 6 open reading frames (ORFs) in comparison with the matching homologous plant protein obtained through tBLASTn above, we found this “novel” protein which we named "PDL1LI". It has the following amino acid sequence: MHAVRRHRGEMHKVALLHNSFLIISILGSYADDFRVMVPTRRLTAARGHSVVLGCEFSPHFGPNPDLSSLVLTWQRQEDSRVVHSFYYERDQLAKQSSAYRNRTALFVTELSKGNASVRIENVGVTDAGRYLCTVSTNQGTNKAELQLDYGAFYTEPRLTINVNSSDVLLQYETEGFPAPVVIWKGEDGENLTDRMKTSVQSNEEMGLYYIKSSYTAPNTPLSLTFTLENHLLHQYLQRPVSYTGGQNSCFYQFIAPVVVS Gor4 shows that our novel PDL1LI protein is 181 amino acids long with 36% alpha helix, 18% extended strand and 46% random coil sequence. According to BLASTp, this protein contains an immunoglobulin domain found in the Ig superfamily in the first half of the protein, and specific domain hits to the Ig_HHLA2, V-set, and IGv domains, with e-values of 1.37e-28, 2.23e-08, and 1.73e-06. Conclusions: Of all the plants, we found a single homology for our original protein PDL1 only in Nicotiana tabacum. We named this novel protein PDL1LI. Tobacco has been implicated in the etiology of several cancers including lung cancer, bladder cancer, head and neck cancers, etc. A wet lab experiment is underway to isolate our novel protein PDL1LI and to study its properties including any possible inhibitory actions on T cells. If confirmed, then we would have elucidated a new carcinogenic mechanism of tobacco.

2002 ◽  
Vol 8 (S02) ◽  
pp. 248-249
Author(s):  
Louise Brisson ◽  
Nathalie Bolduc ◽  
Mario Ouellet ◽  
Frédéric Pitre ◽  
Israel Fortin

2007 ◽  
Vol 6 (11) ◽  
pp. 2001-2008 ◽  
Author(s):  
M. Paoletti ◽  
C. Clavé

ABSTRACT Vegetative incompatibility is a programmed cell death reaction that occurs when fungal cells of unlike genotypes fuse. Genes defining vegetative incompatibility (het genes) are highly polymorphic, and most if not all incompatibility systems include a protein partner bearing the fungus-specific domain termed the HET domain. The nonallelic het-C/het-E incompatibility system is the best-characterized incompatibility system in Podospora anserina. Cell death is triggered by interaction of specific alleles of het-C, encoding a glycolipid transfer protein, and het-E, encoding a HET domain and a WD repeat domain involved in recognition. We show here that overexpression of the isolated HET domain from het-E results in cell death. This cell death is characterized by induction of autophagy, increased vacuolization, septation, and production of lipid droplets, which are hallmarks of cell death by incompatibility. In addition, the HET domain lethality is suppressed by the same mutations as vegetative incompatibility, but not by the inactivation of het-C. These results establish the HET domain as the mediator of cell death by incompatibility and lead to a modular conception of incompatibility systems whereby recognition is ensured by the variable regions of incompatibility proteins and cell death is triggered by the HET domain.


2002 ◽  
Vol 9 (3) ◽  
pp. 309-321 ◽  
Author(s):  
D Serafini-Fracassini ◽  
S Del Duca ◽  
F Monti ◽  
F Poli ◽  
G Sacchetti ◽  
...  

2002 ◽  
Vol 116 (4) ◽  
pp. 548-553 ◽  
Author(s):  
Inês Chaves ◽  
Ana Paula Regalado ◽  
Ming Chen ◽  
Cândido Pinto Ricardo ◽  
Allan M. Showalter

Plant Science ◽  
2015 ◽  
Vol 238 ◽  
pp. 148-157 ◽  
Author(s):  
Amine Yekkour ◽  
Daniel Tran ◽  
Delphine Arbelet-Bonnin ◽  
Joël Briand ◽  
Florence Mathieu ◽  
...  

2005 ◽  
Vol 392 (1) ◽  
pp. 47-54 ◽  
Author(s):  
Dongsheng Liu ◽  
Hongwei Yao ◽  
Yaoyao Chen ◽  
Yingang Feng ◽  
Yingyu Chen ◽  
...  

PDCD5-(1–26) is a N-terminal 26-residue fragment of human PDCD5 (programmed cell death 5) protein. PDCD5 is an important novel protein that regulates both apoptotic and non-apoptotic programmed cell death. The conformation of PDCD5 protein is a stable helical core consisting of a triple-helix bundle and two dissociated terminal regions. The N-terminal region is ordered and contains abundant secondary structure. Overexpression and purification of the N-terminal 26-residure fragment, PDCD5-(1–26), was performed in this study to better understand its tertiary structure. The spectroscopic studies using CD and hetero- and homo-nuclear NMR methods determine a stable α-helix formed by Asp3–Ala19 of PDCD5-(1–26). The N-terminal residues Asp3–Ala19 of PDCD5 were then affirmed to have the capacity to form a stable α-helix independently of the core of the protein. Analysis of the helical peptide of PDCD5-(1–26) indicates that the surface of this well-formed α-helix has a unique electrostatic potential character. This may provide an environment for the N-terminal α-helix of PDCD5 to serve as an independent functional entity of the protein. The apoptosis activity assay shows that the deletion of the N-terminal α-helix of PDCD5 significantly attenuates the apoptosis-promoting effects on HL-60 cells induced by serum withdrawal.


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