分離済み変異体

tm2685

Allele Nametm2685
BalanceCompleted
OutCrossNot Accepted
Sequence NameY57A10A.15
Gene Namepolg-1
Worm BaseAllele Name tm2685 (x1)
Gene Name polg-1
Sequence Y57A10A.15
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype" lethal or sterile
Mutation site Please see gene structure to locate the deletion in relation to exon(s) 62921/62922-63407/63408 (486 bp deletion)
ChromosomeII
Putative gene structurecomplement(join(53507..53659, 53863..54090, 54916..55216, 56472..56874, 57618..57988, 59080..59628, 61225..61582, 61709..61793, 62568..63020, 63272..63589))
Map position6.94
BalancermnC1 [dpy-10(e128) unc52(e444) nIs190 let-?],rol-1 (e91)
Map position of balancer
Sequence of primersExtFwd:GATAAGCCTCCCGACATCTG,IntFwd:CCCGACATCTGGCTCGATCA,ExtRev:GCGTCCTCCGAAAATAATGC,IntRev:CCACGTATCCCGCCGACAAA
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Mazzetto M, Gonzalez LE, Sanchez N, Reinke V.
Characterization of the distribution and dynamics of chromatin states in the C. elegans germline reveals substantial H3K4me3 remodeling during oogenesis.
Genome Res 2024 34(1) 57-69 
[ PubMed ID = 38164610 ] [ RRC reference ]

Meyrick J, Stefanetti RJ, Errington L, McFarland R, Gorman GS, Lax NZ.
Model systems informing mechanisms and drug discovery: a review of POLG-related disease models.
Wellcome Open Res 2023 8 33 
[ PubMed ID = 41199776 ] [ RRC reference ]

Hench J, Bratić Hench I, Pujol C, Ipsen S, Brodesser S, Mourier A, Tolnay M, Frank S, Trifunović A.
A tissue-specific approach to the analysis of metabolic changes in Caenorhabditis elegans.
PLoS One 2011 6(12) e28417 
[ PubMed ID = 22162770 ] [ RRC reference ]

Bratic I, Hench J, Trifunovic A.
Caenorhabditis elegans as a model system for mtDNA replication defects.
Methods 2010 51(4) 437-43 
[ PubMed ID = 20230897 ] [ RRC reference ]

Sugimoto T, Mori C, Takanami T, Sasagawa Y, Saito R, Ichiishi E, Higashitani A.
Caenorhabditis elegans par2.1/mtssb-1 is essential for mitochondrial DNA replication and its defect causes comprehensive transcriptional alterations including a hypoxia response.
Exp Cell Res 2008 314(1) 103-14 
[ PubMed ID = 17900564 ] [ RRC reference ]