Search bioRxiv⌕ Search

bioRxiv · 10.1101/2022.08.31.505262

Diversity, Phylogenetic Relationships, And Expression Profiles Of Invertase Inhibitor Genes In Sweetpotato

Abstract

Invertases and their inhibitor proteins are key regulators of carbon allocation in plants. Manipulation of invertase inhibitor (ITI) activity can potentially increase crop yield. The aim of this study was to determine the sequence diversity, phylogenetic relationships, and expression profiles of ITI genes in sweetpotato(Ipomoea batatas).. The coding sequences of two ITI paralogs (SPITI1 and SPITI2) were cloned from two sweetpotato varieties (Beauregard and Jewel) and sequenced. The DNA sequences were used to deduce amino acids sequences and predicted protein properties. Quantitative PCR (qPCR) was carried out to study the expression profiles of the genes at different developmental stages. The results show that introns are absent in both SPITI paralogs. SNPs, Indels, and variable simple sequence repeats (SSR) were present in the SPITI1 paralog, however, only SNPs were identified in the SPITI2 paralog. The predicted SPITI1 protein had 168, 172, or 174 amino acid residues, and molecular weights ranging from 17.88 to 18.38 kDa. In contrast, SPITI2 coded for a protein with 192 amino acid residues, with molecular weight ranging from 20.59 to 20.65 kDa. All conserved domains of ITI proteins were present in both protein isoforms. Phylogenetic analysis indicated that SPITI genes were more closely related to I.trifida and I.triloba than I.nil, thus, suggesting their evolutionary relationship and conservation. A qPCR study indicated that both SPITI genes were expressed in all the sample tissues, though relative expression values differed across tissues at different developmental stages. This is the first study reporting diversity of SPITI genes and of an ~18 kDA isoform in sweetpotato. The findings may enable design of genetic engineering strategies for SPITI genes, including CRISPR/Cas gene editing in sweetpotato.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Acheampong, S., Sederoff, H., Olukolu, B. A., Asare, A., Yencho, G.. 2022-08-31. Diversity, Phylogenetic Relationships, And Expression Profiles Of Invertase Inhibitor Genes In Sweetpotato. https://doi.org/10.1101/2022.08.31.505262

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Fatty Acid Synthase Binds Cellular mRNAs and its Depletion Reduces Translational Efficiency

Metabolic enzymes with non-canonical RNA binding activity have drawn a growing interest, due to their implications for basic biology and disease. Here we present the first endogenous RNA interactome of fatty acid synthase (FASN), an emerging oncological and virological target. Utilizing crosslinking-based approaches, we characterize the direct RNA association of FASN in two human cell lines, identifying over 6000 binding sites across over 3500 protein-coding genes, with a striking preference for the 5' UTR. We provide a functional cross-screen on the effects of FASN depletion on cellular translation. This integration with ribosome profiling indicated a preferential reduction in the translational efficiencies of FASN-associated mRNAs - an effect shown to be dependent on binding location and site number. Associated transcripts were enriched for morphogenic and cell division-related functions, as well as palmitoylated proteins. This correlative work primes further investigation of FASN as a regulator of translation of its target mRNAs.

molecular biology↗

Genomic features and instability of linezolid resistance in vancomycin-resistant Enterococcus faecalis ST525

This study investigated the mechanisms of oxazolidinone resistance and genomic background in clinical ST525 Enterococcus faecalis isolates, a poorly characterized lineage reported in Brazilian hospitals as either vancomycin-resistant (VRE) or linezolid- and vancomycin-resistant (LVRE). Five LVREfs from intensive care unit patients (linezolid MICs, 8-32 mg/L; vancomycin MICs, >256 mg/L) carried only G2576T and G2505A (in three of four rrl copies) as known linezolid resistance determinants, despite variable linezolid MICs. During serial in vitro passages without antibiotic pressure, isolates with initial MICs of 8-16 mg/L exhibited progressive MIC reductions accompanied by reversion of mutant to wild-type rrl copies, whereas the isolate with an initial MIC of 32 mg/L maintained high-level resistance without reversion. Additional domain V substitutions emerged during MIC decline, while growth kinetics remained broadly similar. Whole-genome sequencing of a representative isolate (LVREfs L7) revealed a ~2.8-Mb chromosome enriched in mobile genetic elements (~8.6%), lacking a functional CRISPR-Cas system. A plasmid-borne prototype Tn1546 carrying vanA, devoid of internal insertion sequences, was found inserted into a Tn3-family transposase gene, a platform not typically associated with vanA mobilization. Together, these findings indicate that ST525 LVREfs, whose genomic features are consistent with long-term persistence in hospitals, may pose a challenge to routine susceptibility testing. A single mutational mechanism can yield variable linezolid MICs, and the ratio of mutated vs wild-type rrl copies can become heterogeneous in the absence of antibiotic pressure, without correlating directly with these values, contrary to the well-documented copy number-MIC correlation.

molecular biology↗

Global repression of mesenchymal genes in epithelial cells by the histone demethylase LSD1

Epithelial-mesenchymal transition (EMT) is an essential process in development, tissue repair, and tumour metastasis, and is triggered by SNAI, ZEB and TWIST transcription factors, that recruit lysine-specific demethylase 1 (LSD1) to repress epithelial genes such as E-cadherin. In mesenchymal cells, LSD1 inhibition restores E-cadherin expression and reduces migration and invasion, consistent with LSD1 inhibition reverting EMT, and offering a therapeutic modality for EMT-associated disease. Recent data, however, suggest context-dependent roles for LSD1, as its inhibition in epithelial cells increases mesenchymal marker expression, potentially promoting EMT. To investigate this discrepancy, we mapped genome-wide binding of LSD1 in HCT116 epithelial cells and used rapid degron-mediated ablation of endogenous LSD1 to measure changes in nascent and steady-state transcription and chromatin accessibility. In epithelial cells, LSD1 binds constitutively-accessible, primed mesenchymal promoters. These are rapidly derepressed after LSD1 ablation, with activation of SNAI2 and ZEB1, which repress epithelial hallmarks such as E-cadherin. Re-introduction of LSD1 downregulates SNAI2 and ZEB1 but, surprisingly, further represses E-cadherin, indicating sustained loss of epithelial characteristics. Collectively, our results show that LSD1 maintains epithelial identity by repressing mesenchymal genes, questioning the therapeutic utility of LSD1 inhibition for EMT control.

molecular biology↗