RpI135, Rpl135, DmRP135, RNA polymerase I
Please see the JBrowse view of Dmel\Polr1B for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.52
3.6 (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
1129 (aa)
Component of the RNA polymerase I (Pol I) complex consisting of at least 13 subunits.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Polr1B using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: maternally deposited
A 3.6 kb transcript is detected in Northern blots of adult mRNA.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Polr1B in JBrowse




2-0.7
2-0.0
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
polyclonal
dsRNA made from templates generated with primers directed against this gene in combination with dsRNA against gig results in suppression of the final average cell size, with it being closer to the control average cell size, rather than the average cell size resulting from knockdown of the candidate gene alone.
In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.
Based on biochemical evidence, it has been shown that RpI135 encodes the second largest subunit of RNA polymerase I, and not the equivalent subunit of RNA polymerase III, as previously reported (FBrf0050568).
Isolated as a clone having weak homology to the 150kD subunit of yeast RNA polymerase II.
RpI135, encoding the second largest subunit of RNA polymerase II, has been cloned and sequenced.
Source for merge of: RpI135 l(2)k16513
Source for identity of: RpI135 CG4033
Source for identity of: Polr1B RpI135
Named 'Polr1B' after the human ortholog.