l(2)34De, pol γ-β, MtPolB, l(2)br16, DNApol-γ
Please see the JBrowse view of Dmel\PolG2 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 5.41
Gene model reviewed during 5.52
Multiphase exon postulated: this gene shares a region of coding sequence with an overlapping gene, but different reading frames are utilized in the overlapping coding region.
There is only one protein coding transcript and one polypeptide associated with this gene
Mitochondrial DNA polymerase was purified to near
homogeneity from early embryos. It is a heterodimer consisting of two
subunits of 125kD and 35kD. The large subunit contains the DNA-polymerase
activity.The DNA polymerase utilizes a large variety of template-primers
efficiently.
Component of the DNA polymerase gamma complex consisting of two subunits: the catalytic subunit DNApol-gamma/DNApolG1 and the accessory subunit PolG2/DNApol-gamma35.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\PolG2 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\PolG2 in JBrowse2-49
2-45.1
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.
Multiple amino acid sequence alignments show the DNA polymerases from numerous species forms a family strongly conserved from yeast to man.
Subunit structure and enzymatic activity of DNA polymerase γ are studied using a combination of physical and immunological approaches. The role of the 2 subunits in template primer DNA binding is explored.
mtSSB stimulates DNA polymerase γ activity in vitro.
The rate and processivity of DNA synthesis by DNA polymerase γ has been analysed under a variety of different conditions.
Biochemical description of the 3'->5' exonuclease associated with mitochondrial DNA polymerase.
The 3' to 5' exonuclease encoded provides a proof reading function to enhance the fidelity of DNA synthesis during mitochondrial DNA replication.
A structural and mechanistic analysis of DNApol-γ125 and DNApol-γ35 demonstrates them to be both effective and accurate in the synthesis of DNA.
Comparison of the rate and specificity of DNA synthesis by DNApol-γ125 and DNApol-γ35 on several template primers, and an examination of the products of DNA synthesis has been carried out.
DNApol-γ125 and DNApol-γ35 have been isolated and purified and their subunit structure and catalytic properties examined.
Source for merge of: MtPolB l(2)34De
Dicistronic annotation CG33084 split out into separate annotations for each open reading frame, CG33649 and CG33650 in release 4.2 of the genome annotation. CG33650 corresponds to DNApol-γ35.
One or more of the processed transcripts for this gene contain(s) two non-overlapping open reading frames (ORFs). The non-overlapping ORFs are represented by CG33649 and DNApol-γ35.
The identity of l(2)34De and MtPolB is based on mapping with T(2;3)b89e12 ordering l(2)34De and RpII33.
Source for identity of: PolG2 DNApol-γ35