Recognition of Translation Initiation Sites in Arabidopsis Thaliana

Author(s):  
Haitham Ashoor ◽  
Arturo M. Mora ◽  
Karim Awara ◽  
Boris R. Jankovic ◽  
Rajesh Chowdhary ◽  
...  

Their results suggest that in spite of the considerable evolutionary distance between Homo sapiensand A. thaliana, our approach successfully recognized deeply conserved genomic signals that characterize TIS. Moreover, they report the highest accuracy of TIS recognition in A. thaliana DNA genomic sequences.

2019 ◽  
Vol 11 (11) ◽  
pp. 3194-3206 ◽  
Author(s):  
Yulong Wei ◽  
Xuhua Xia

Abstract Microorganisms require efficient translation to grow and replicate rapidly, and translation is often rate-limited by initiation. A prominent feature that facilitates translation initiation in bacteria is the Shine–Dalgarno (SD) sequence. However, there is much debate over its conservation in Cyanobacteria and in chloroplasts which presumably originated from endosymbiosis of ancient Cyanobacteria. Elucidating the utilization of SD sequences in Cyanobacteria and in chloroplasts is therefore important to understand whether 1) SD role in Cyanobacterial translation has been reduced prior to chloroplast endosymbiosis or 2) translation in Cyanobacteria and in plastid has been subjected to different evolutionary pressures. To test these alternatives, we employed genomic, proteomic, and transcriptomic data to trace differences in SD usage among Synechocystis species, Microcystis aeruginosa, cyanophages, Nicotiana tabacum chloroplast, and Arabidopsis thaliana chloroplast. We corrected their mis-annotated 16S rRNA 3′ terminus using an RNA-Seq-based approach to determine their SD/anti-SD locational constraints using an improved measurement DtoStart. We found that cyanophages well-mimic Cyanobacteria in SD usage because both have been under the same selection pressure for SD-mediated initiation. Whereas chloroplasts lost this similarity because the need for SD-facilitated initiation has been reduced in plastids having much reduced genome size and different ribosomal proteins as a result of host-symbiont coevolution. Consequently, SD sequence significantly increases protein expression in Cyanobacteria but not in chloroplasts, and only Cyanobacterial genes compensate for a lack of SD sequence by having weaker secondary structures at the 5′ UTR. Our results suggest different evolutionary pressures operate on translation initiation in Cyanobacteria and in chloroplast.


Plant Science ◽  
2001 ◽  
Vol 161 (4) ◽  
pp. 685-693 ◽  
Author(s):  
Henri De Greve ◽  
Viet Khong Nguyen ◽  
Francine Deboeck ◽  
Lin Thia-Toong ◽  
Mansour Karimi ◽  
...  

2022 ◽  
Vol 12 ◽  
Author(s):  
Patrick Willems ◽  
Elvis Ndah ◽  
Veronique Jonckheere ◽  
Frank Van Breusegem ◽  
Petra Van Damme

Alternative translation initiation is a widespread event in biology that can shape multiple protein forms or proteoforms from a single gene. However, the respective contribution of alternative translation to protein complexity remains largely enigmatic. By complementary ribosome profiling and N-terminal proteomics (i.e., riboproteogenomics), we provide clear-cut evidence for ~90 N-terminal proteoform pairs shaped by (alternative) translation initiation in Arabidopsis thaliana. Next to several cases additionally confirmed by directed mutagenesis, identified alternative protein N-termini follow the enzymatic rules of co-translational N-terminal protein acetylation and initiator methionine removal. In contrast to other eukaryotic models, N-terminal acetylation in plants cannot generally be considered as a proxy of translation initiation because of its posttranslational occurrence on mature proteolytic neo-termini (N-termini) localized in the chloroplast stroma. Quantification of N-terminal acetylation revealed differing co- vs. posttranslational N-terminal acetylation patterns. Intriguingly, our data additionally hints to alternative translation initiation serving as a common mechanism to supply protein copies in multiple cellular compartments, as alternative translation sites are often in close proximity to cleavage sites of N-terminal transit sequences of nuclear-encoded chloroplastic and mitochondrial proteins. Overall, riboproteogenomics screening enables the identification of (differential localized) N-terminal proteoforms raised upon alternative translation.


PLoS ONE ◽  
2012 ◽  
Vol 7 (2) ◽  
pp. e31606 ◽  
Author(s):  
Ana Valeria Martínez-Silva ◽  
César Aguirre-Martínez ◽  
Carlos E. Flores-Tinoco ◽  
Naholi D. Alejandri-Ramírez ◽  
Tzvetanka D. Dinkova

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