Strain Data Sheet

RBRC02759

Strain Information

Image
BRC No.RBRC02759
TypeTargeted Mutation CongenicCartagena
SpeciesMus musculus
Strain nameB6.Cg-Atg7<tm1Tchi>
Former Common nameC57BL/6-Atg7 flox/flox
H-2 Haplotype
ES Cell lineTT2 [(C57BL/6NCrlj x CBA/JNCrlj)F1]
Background strain
Appearanceblack [a/a B/B C/C]
Strain developmentDeveloped by Masaaki Komatsu and Tomoyuki Chiba, Tokyo Metropolitan Institute of Medical Science. The targeting construct was electoroporated into TT2 ES cells derived from (C57BL/6 x CBA)F1. The mice were backcrossed to C57BL/6 over 5 times.
Strain descriptionAtg7, autophagy-related 7 gene floxed mice. A targeting vector was constructed by insertion of a loxP site within introns 13 and 14. Exon 14 was fused to a cDNA fragment encoded by exons 15, 16 and 17 and polyA after the stop codon. Atg7 is essential for ATG conjugation, LC3 modification systems, and autophagosome formation. Conditional Atg7 deficient mice can be generated by crossing with tissue-specific Cre mice.
Colony maintenanceHomozygote x Homozygote [or Crossing to C57BL/6JJcl]. Homozygous mutant mice are viable and fertile.
References
Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice.
Komatsu M, Waguri S, Ueno T, Iwata J, Murata S, Tanida I, Ezaki J, Mizushima N, Ohsumi Y, Uchiyama Y, Kominami E, Tanaka K, Chiba T
J. Cell Biol., 169, 425-434 (2005) 15866887

Health Report

Examination Date / Room / Rack2024/04/08Room:3-BRack:K
2024/01/09Room:3-BRack:K
2023/10/10Room:3-BRack:K
2023/07/10Room:3-BRack:K
2023/06/26Room:3-BRack:K
2023/06/26Room:3-BRack:K
2023/04/10Room:3-BRack:K
2023/01/10Room:3-BRack:K
2022/10/11Room:3-BRack:K

Gene

Gene SymbolGene NameChr.Allele SymbolAllele NameCommon NamesPromoterDiseases Related to This Gene
Atg7autophagy related 76Atg7targeted mutation 1, Tomaki Chiba
  • spinocerebellar ataxia, autosomal recessive 31(MedGEN)
  • loxPphage P1 loxP6loxP
  • spinocerebellar ataxia, autosomal recessive 31(MedGEN)
  • loxPphage P1 loxP6loxP
  • spinocerebellar ataxia, autosomal recessive 31(MedGEN)
  • neoneomycin resistance gene (E. coli)6herpes simplex virus thymidine kinase promoter (HSV tk promoter)
  • spinocerebellar ataxia, autosomal recessive 31(MedGEN)
  • Phenotype

    Annotation by Mammalian phenotyhpe ontology
  • abnormal amino acid level(MP:0005332)

  • abnormal autophagy(MP:0008260)

  • abnormal circulating enzyme level(MP:0001570)

  • abnormal common lymphocyte progenitor cell morphology(MP:0008249)

  • abnormal hematopoietic stem cell morphology(MP:0004808)
  • more 29 phenotypes
  • abnormal hematopoietic stem cell physiology(MP:0010763)

  • abnormal hepatocyte morphology(MP:0000607)

  • abnormal leukocyte morphology(MP:0008246)

  • abnormal liver morphology(MP:0000598)

  • abnormal liver physiology(MP:0000609)

  • abnormal motor neuron morphology(MP:0000937)

  • abnormal nervous system physiology(MP:0003633)

  • absent cerebral cortex pyramidal cells(MP:0009975)

  • absent hippocampus pyramidal cells(MP:0009972)

  • axon degeneration(MP:0005405)

  • behavior/neurological phenotype(MP:0005386)

  • decreased B cell number(MP:0005017)

  • decreased NK cell number(MP:0008045)

  • decreased T cell number(MP:0005018)

  • decreased bone marrow cell number(MP:0000333)

  • decreased common myeloid progenitor cell number(MP:0008813)

  • decreased hematopoietic stem cell number(MP:0004810)

  • decreased leukocyte cell number(MP:0000221)

  • decreased liver function(MP:0003325)

  • enlarged liver(MP:0000599)

  • increased circulating alanine transaminase level(MP:0002941)

  • increased circulating alkaline phosphatase level(MP:0002968)

  • increased circulating aspartate transaminase level(MP:0005343)

  • increased hepatocyte proliferation(MP:0003893)

  • increased liver weight(MP:0002981)

  • increased neuron apoptosis(MP:0003203)

  • limb grasping(MP:0001513)

  • tremors(MP:0000745)

  • weight loss(MP:0001263)
  • Detailed phenotype data

    Ordering Information

    供与核酸Polyoma enhancer/herpes simplex virus thymidine kinase gene (MC1) promoter, E. coli Neomycin resistance gene, Phage P1 loxP sites, Mouse Atg7 genomic DNA
    Research application
    提供条件条件を付加する。利用者は事前に寄託者の提供承諾書を得る。
    研究成果の公表にあたって寄託者の指定する文献を引用する。J. Cell Blol., 169, 425-434 (2005).
    研究成果の公表にあたって謝辞の表明を必要とする。
    公表を前提とした学術研究に限る。営利機関の使用にあたっては事前に寄託者からの許可を得ること。利用者が本件リソースを使用して得られた研究成果に基づき特許等の申請、及び事業活動を行う場合は、寄託者と別途協議を行う。
    Depositor小松 雅明((財)東京都医学研究機構)
    Strain Status生体のアイコン生体
    凍結胚のアイコン凍結胚
    凍結精子のアイコン凍結精子
    Strain Availability凍結精子を1ヶ月以内に提供可能
    凍結胚を1ヶ月以内に提供可能
    生体マウスを3~6ヶ月以内に提供可能
    Additional Info.Necessary documents for ordering:
    1. Approval form (Japanese / English)
    2. Order form (Japanese / English)
    3. Category I MTA: MTA for distribution with RIKEN BRC (Japanese / English)
    4. Acceptance of responsibility for living modified organism (Japanese / English)
    Lab HP (Japanese)
    Genotyping protocol -PCR-
    Mouse of the Month Jun 2012, Mouse of the Month Oct 2016

    BRC mice in Publications

    Williams PA, Naughton KE, Simon LA, Soto GE, Parham LR, Ma X, Danan CH, Hu W, Friedman ES, McMillan EA, Mehta H, Stoltz MA, Soto Ocaña J, Zackular J, Bittinger K, Whelan KA, Karakasheva TA, Hamilton KE.
    Intestinal epithelial autophagy is required for the regenerative benefit of calorie restriction.
    Am J Physiol Gastrointest Liver Physiol (2023) 36852920
    Luo P, Yan H, Du J, Chen X, Shao J, Zhang Y, Xu Z, Jin Y, Lin N, Yang B, He Q.
    PLK1 (polo like kinase 1)-dependent autophagy facilitates gefitinib-induced hepatotoxicity by degrading COX6A1 (cytochrome c oxidase subunit 6A1).
    Autophagy 17(10) 3221-3237(2021) 33315519
    Muralimanoharan S, Gao X, Weintraub S, Myatt L, Maloyan A.
    Sexual dimorphism in activation of placental autophagy in obese women with evidence for fetal programming from a placenta-specific mouse model.
    Autophagy 12(5) 752-69(2016) 26986453
    Wang Y, Liu X, Zhu L, Li W, Li Z, Lu X, Liu J, Hua W, Zhou Y, Gu Y, Zhu M.
    PG545 alleviates diabetic retinopathy by promoting retinal Müller cell autophagy to inhibit the inflammatory response.
    Biochem Biophys Res Commun 531(4) 452-458(2020) 32800548
    Mizushima N, Yoshimori T, Levine B.
    Methods in mammalian autophagy research.
    Cell 140(3) 313-26(2010) 20144757
    Song ZH, Yu HY, Wang P, Mao GK, Liu WX, Li MN, Wang HN, Shang YL, Liu C, Xu ZL, Sun QY, Li W.
    Germ cell-specific Atg7 knockout results in primary ovarian insufficiency in female mice.
    Cell Death Dis 6(1) e1589(2015) 25590799
    Yan B, Belke D, Gui Y, Chen YX, Jiang ZS, Zheng XL.
    Pharmacological inhibition of MALT1 (mucosa-associated lymphoid tissue lymphoma translocation protein 1) induces ferroptosis in vascular smooth muscle cells.
    Cell Death Discov 9(1) 456(2023) 38097554
    Walter KM, Schönenberger MJ, Trötzmüller M, Horn M, Elsässer HP, Moser AB, Lucas MS, Schwarz T, Gerber PA, Faust PL, Moch H, Köfeler HC, Krek W, Kovacs WJ.
    Hif-2α promotes degradation of mammalian peroxisomes by selective autophagy.
    Cell Metab 20(5) 882-897(2014) 25440060
    Klochkova A, Karami AL, Fuller AD, Parham LR, Panchani SR, Natarajan S, Jackson JL, Mu A, Tan Y, Cai KQ, Klein-Szanto AJ, Muir AB, Tétreault MP, Graña X, Hamilton KE, Whelan KA.
    Autophagy Contributes to Homeostasis in Esophageal Epithelium Where High Autophagic Vesicle Level Marks Basal Cells With Limited Proliferation and Enhanced Self-Renewal Potential.
    Cell Mol Gastroenterol Hepatol 18(1) 15-40(2024) 38452871
    Parham LR, Williams PA, Katada K, Nettleford SK, Chatterji P, Acheampong KK, Danan CH, Ma X, Simon LA, Naughton KE, Karakasheva T, McMillan EA, Whelan KA, Brady DC, Shaffer SM, Hamilton KE.
    IGF2BP1/IMP1 deletion enhances a facultative stem cell state via regulation of MAP1LC3B.
    Cell Mol Gastroenterol Hepatol (2023) 38081361
    Wang H, Wan H, Li X, Liu W, Chen Q, Wang Y, Yang L, Tang H, Zhang X, Duan E, Zhao X, Gao F, Li W.
    Atg7 is required for acrosome biogenesis during spermatogenesis in mice.
    Cell Res 24(7) 852-69(2014) 24853953
    Bang S, Lee GK, Shin H, Suh CS, Lim HJ.
    Vitrification, in vitro fertilization, and development of Atg7 deficient mouse oocytes.
    Clin Exp Reprod Med 43(1) 9-14(2016) 27104152
    Chatterji P, Williams PA, Whelan KA, Samper FC, Andres SF, Simon LA, Parham LR, Mizuno R, Lundsmith ET, Lee DS, Liang S, Wijeratne HS, Marti S, Chau L, Giroux V, Wilkins BJ, Wu GD, Shah P, Tartaglia GG, Hamilton KE.
    Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1.
    EMBO Rep 20(6) (2019) 31061170
    Kang X, Yang W, Feng D, Jin X, Ma Z, Qian Z, Xie T, Li H, Liu J, Wang R, Li F, Li D, Sun H, Wu S.
    Cartilage-Specific Autophagy Deficiency Promotes ER Stress and Impairs Chondrogenesis in PERK-ATF4-CHOP-Dependent Manner.
    J Bone Miner Res 32(10) 2128-2141(2017) 28304100
    Li KC, Wang CH, Zou JJ, Qu C, Wang XL, Tian XS, Liu HW, Cui T.
    Loss of Atg7 in Endothelial Cells Enhanced Cutaneous Wound Healing in a Mouse Model.
    J Surg Res 249 145-155(2020) 31958599
    Zhang Y, Cross SD, Stanton JB, Marmorstein AD, Le YZ, Marmorstein LY.
    Early AMD-like defects in the RPE and retinal degeneration in aged mice with RPE-specific deletion of Atg5 or Atg7.
    Mol Vis 23 228-241(2017) 28465655
    Song Y, Na H, Lee SE, Kim YM, Moon J, Nam TW, Ji Y, Jin Y, Park JH, Cho SC, Lee J, Hwang D, Ha SJ, Park HW, Kim JB, Lee HW.
    Dysfunctional adipocytes promote tumor progression through YAP/TAZ-dependent cancer-associated adipocyte transformation.
    Nat Commun 15(1) 4052(2024) 38744820
    Tan HWS, Lu G, Dong H, Cho YL, Natalia A, Wang L, Chan C, Kappei D, Taneja R, Ling SC, Shao H, Tsai SY, Ding WX, Shen HM.
    A degradative to secretory autophagy switch mediates mitochondria clearance in the absence of the mATG8-conjugation machinery.
    Nat Commun 13(1) 3720(2022) 35764633
    Luciani A, Schumann A, Berquez M, Chen Z, Nieri D, Failli M, Debaix H, Festa BP, Tokonami N, Raimondi A, Cremonesi A, Carrella D, Forny P, Kölker S, Diomedi Camassei F, Diaz F, Moraes CT, Di Bernardo D, Baumgartner MR, Devuyst O.
    Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency.
    Nat Commun 11(1) 970(2020) 32080200