nrelated to Bt-resistance coding genes (FigureBt-resistance related gene was much less than one hundred kb up- or downstream in the lncRNA (Figure 4A ). The BRD3 list proximal CYP was 7.868 kb from lncRNA LOC11350610 (this lncRNA was upregulated) (Figure 4A), the proximal ABC transporter 50.672 kb from lncRNA LOC110369725 (this lncRNA was downregulated) (Figure 4B), and also the serine protease 0.646 kb from lncRNA LOC110382674 (this lncRNA was discovered only within the resistant strain) (Figure 4C). The lncRNA presented in Figure 4D was downregulated, along with the lncRNA presented in Figure 4E was identified only in the susceptible strain.Insects 2022, 13,(Figure 4E). Each and every proximal Bt-resistance linked gene was less than one hundred kb up- or downstream in the lncRNA (Figure 4A ). The proximal CYP was 7.868 kb from lncRNA LOC11350610 (this lncRNA was upregulated) (Figure 4A), the proximal ABC transporter 50.672 kb from lncRNA LOC110369725 downstream was downregulated) resistance related gene was significantly less than 100 kb up- or (this lncRNAfrom the lncRNA (Fig(Figure 4B), and the serine protease 0.646 from lncRNA LOC11350610 (this lncRNA was ure 4A ). The proximal CYP was 7.868 kbkb from lncRNA LOC110382674 (this lncRNA of 18 was found only in the resistant proximal ABC transporter 50.672 kb in Figure9 4D upregulated) (Figure 4A), the strain) (Figure 4C). The lncRNA presentedfrom lncRNA was downregulated,lncRNA was downregulated)in Figure4B), plus the serine protease plus the lncRNA presented (Figure 4E was located only within the LOC110369725 (this susceptible strain. 0.646 kb from lncRNA LOC110382674 (this lncRNA was located only inside the resistant strain) (Figure 4C). The lncRNA presented in Figure 4D was downregulated, and the lncRNA presented in Figure 4E was found only in the susceptible strain.Figure 3. Workflow for identifying statistically differentiated JAK Formulation lncRNAs coding genes in toto and Figure three. Workflow for identifying statistically in Bt-resistance lncRNAs proximal in toto and these Figure with functions recognized to have a role differentiated lncRNAsare coding genesstatistically those 3. Workflow for identifying statistically differentiated that coding genes to in toto and with with functions known to have ain Bt-resistance which are proximal size to statistically differendifferentiated recognized to possess a role part in Bt-resistance which might be proximal from the scaffolds, even these functions lncRNAs. Proximity measurements had been limited by theto statistically differentiated lncRNAs. Proximity measurements million base by thecis plus the scaffolds,scaffolds, even though even though proximity is defined as 1 have been limited pairs by of size from despite the fact that proximity tiated lncRNAs. Proximity measurements were limitedsize the trans of the the lncRNA. For every proximal as 1 million and lncRNA, a BLASTn alignment was lncRNA. For every coding gene and proximity is defined as base pairsbase pairs cis and trans lncRNA. also every single proximalproximal coding is defined coding gene 1 million cis and trans from the in the For performed to assess possible pseudogenes. gene and lncRNA, a alignment was also carried out to assess potential potential pseudogenes. lncRNA, a BLASTn BLASTn alignment was also carried out to assess pseudogenes.(A)Figure 4. Cont.Insects 2022, 13, 12 Insects 2022, 1, x10 of 18 ten of(B)(C)Figure 4. Cont.Insects 2022, 13, 12 Insects 2022, 1, x11 of 18 11 of(D)(E)Figure 4. Genomic scaffold for lncRNAs and identification of proximal protein-coding genes. The Figure four. Genomic scaffold for lncRNAs and id
