Strain Name:
STOCK Malat1tm1.1Svdi/Mmnc
Stock Number:
069938-UNC
Citation ID:
RRID:MMRRC_069938-UNC
Other Names:
Malat1 KO

Strain Information

Malat1tm1.1Svdi
Name: metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA); targeted mutation 1.1, Sven Diederichs
Type: Allele
Species: Mus musculus
Chromosome: 19
Alteration at locus: Knockout
Malat1
Name: metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA)
Synonyms: 2210401K01Rik, 9430072K23Rik, NEAT2
Type: Gene
Species: Mus musculus
Chromosome: 19
Alteration at locus: Knockout
NCBI: 72289
Genetic Alterations
The complete Malat1 6,982 bp of coding sequence, including 250 nucleotides upstream of the transcriptional start site and 321 nucleotides following the 3'-end of the transcript, was flanked by loxP sites. A FRT-flanked neomycin cassette was inserted downstream of the coding sequence but upstream of the second loxP site. Cre-mediated recombination removed the entire floxed region. qRT-PCR confirmed absence of transcripts in various organs.
Genotype Determination
  • Genotyping Protocol(s)
  • Center protocol and contact for technical support will be shipped with mice.
  • ES Cell Line

    v6.5

    Phenotype
    Mice homozygous for this knockout allele are viable and fertile under basal conditions but show cardiovascular phenotypes when challenged. Furthermore, they have reduced neonatal regenerative capacity.
    MeSH Terms
    • Animals
    • Cell Nucleus/metabolism
    • Cell Survival
    • Gene Knockout Techniques
    • Humans
    • Liver Neoplasms/metabolism
    • Liver Neoplasms/pathology
    • Lung Neoplasms/metabolism
    • Lung Neoplasms/pathology
    • Mice
    • Mice, Knockout
    • RNA, Long Noncoding/genetics
    • RNA, Long Noncoding/metabolism
    • Cell Cycle Proteins/genetics
    • Cell Cycle Proteins/metabolism
    • Cell Movement
    • Cell Proliferation
    • Cells, Cultured
    • Disease Models, Animal
    • Endothelial Cells/metabolism
    • Gene Expression Regulation
    • Hindlimb
    • Human Umbilical Vein Endothelial Cells/metabolism
    • Ischemia/genetics
    • Ischemia/metabolism
    • Ischemia/physiopathology
    • Mice, Inbred C57BL
    • Muscle, Skeletal/blood supply
    • Neovascularization, Physiologic
    • Oligonucleotides/genetics
    • Oligonucleotides/metabolism
    • RNA Interference
    • Retinal Neovascularization/genetics
    • Retinal Neovascularization/metabolism
    • Retinal Neovascularization/physiopathology
    • Signal Transduction
    • Transfection
    • Aorta/metabolism
    • Aorta/pathology
    • Aortitis/genetics
    • Aortitis/metabolism
    • Aortitis/pathology
    • Atherosclerosis/genetics
    • Atherosclerosis/metabolism
    • Atherosclerosis/pathology
    • Bone Marrow Cells/metabolism
    • Bone Marrow Cells/pathology
    • Bone Marrow Transplantation
    • Case-Control Studies
    • Down-Regulation
    • Hematopoiesis
    • Mice, Knockout, ApoE
    • MicroRNAs/genetics
    • MicroRNAs/metabolism
    • Plaque, Atherosclerotic
    Strain Development

    A targeting vector (5'-arm-loxP-Malat1-FRT-Neo-FRT-loxP-3'-arm) was linearized and electroporated into the embryonic stem cell (ES) line V6.5 (SV129 × Bl6 F1 hybrid). G418-resistant ES clones were screened for correct homologous recombination at the Malat1 locus via colony PCR and Southern Blot analysis. Positive ES cell clones were injected into blastocysts derived from C57BL/6J mice (Charles River), and chimeric animals were set up for breeding with wildtype C57BL/6J mice to identify animals transmitting the correctly targeted Malat1 locus via the germ line. The heterozygous Malat1loxP,FRTNeo/+ mice generated from the ES cell clones were crossed with a transgenic CMV-Cre deleter line (in a C57Bl/6J genetic background) to remove the PGK-Neo selection cassette and the complete Malat1 gene, which was confirmed by PCR. As a result, nucleotides 5795370–5802920 from mouse chromosome 19qA(Assembly NCBI37/mm9) consisting of the complete 6982 nt Malat1 transcript sequence plus 251 nt upstream of the Malat1 transcription start site and 322 nt downstream of the Malat1 transcript end were removed.
    Mice were interbred. The genetic background appears to be primarily B6J, but an undetermined amount of 129 is likely to be present.

    Suggested Control Mice
    WT litter mates
    MMRRC Genetic QC Summary
    The MMRRC Centers have developed a genetic QC pipeline using MiniMUGA array genotyping to provide additional information on strain backgrounds for MMRRC congenic and inbred strains. For more information on when data may be available, or to request genotyping for a strain of interest, please contact mmrrc@med.unc.edu. Older strains may not have this information.
    • Cardiovascular
    • Developmental Biology
    • Immunology and Inflammation
    Donor
    Stefan Günther, Ph.D., Max Planck for Heart and Lung Research.
    Primary Reference

    Eißmann M, Gutschner T, Hämmerle M, Günther S, Caudron-Herger M, Groß M, Schirmacher P, Rippe K, Braun T, Zörnig M, Diederichs S. Loss of the abundant nuclear non-coding RNA MALAT1 is compatible with life and development. RNA Biol. 2012 Aug;9(8):1076-87. doi: 10.4161/rna.21089. Epub 2012 Aug 1. (Medline PMID: 22858678)

    Michalik KM, You X, Manavski Y, Doddaballapur A, Zörnig M, Braun T, John D, Ponomareva Y, Chen W, Uchida S, Boon RA, Dimmeler S. Long noncoding RNA MALAT1 regulates endothelial cell function and vessel growth. Circ Res. 2014 Apr 25;114(9):1389-97. doi: 10.1161/CIRCRESAHA.114.303265. Epub 2014 Mar 6. (Medline PMID: 24602777)

    Cremer S, Michalik KM, Fischer A, Pfisterer L, Jaé N, Winter C, Boon RA, Muhly-Reinholz M, John D, Uchida S, Weber C, Poller W, Günther S, Braun T, Li DY, Maegdefessel L, Perisic Matic L, Hedin U, Soehnlein O, Zeiher A, Dimmeler S. Hematopoietic Deficiency of the Long Noncoding RNA MALAT1 Promotes Atherosclerosis and Plaque Inflammation. Circulation. 2019 Mar 5;139(10):1320-1334. doi: 10.1161/CIRCULATIONAHA.117.029015. Erratum in: Circulation. 2019 Jul 16;140(3):e161. (Medline PMID: 30586743)

    Colony and Husbandry Information

    Colony Surveillance Program and Current Health Reports

    Mice recovered from a cryo-archive will have health surveillance performed on recipient females. Health reports will be provided prior to shipment. If you require additional health status information, please email mmrrc_health@med.unc.edu.
    Coat Color
    Black
    Eye
    Black
    MMRRC Breeding System
    Random intra-strain mating
    Generation
    N/A
    Overall Breeding Performance
    Good
    Viability and Fertility: Female Male Comments
    Homozygotes are viable: Yes Yes
    Homozygotes are fertile: Yes Yes
    Heterozygotes are fertile: Yes Yes
    Age Reproductive Decline: Undetermined Undetermined
    Average litter size
    7 to 9
    Recommended wean age
    3 Weeks
    Average Pups Weaned
    7 to 9

    Order Request Information

    Limited quantities of breeder mice (recovered litter) are available from a cryoarchive; recovered litter usually available to ship in 3 to 4 months.

    Cryopreserved material may be available upon request, please inquire to mmrrc@med.unc.edu for more information.

    Distribution of this strain requires submission of the MMRRC Conditions of Use (COU). A link to the COU web form will be provided via email after an order has been placed; the form should be completed then or the email forwarded to your institutional official for completion.

    Additional charges may apply for any special requests. Shipping costs are in addition to the basic distribution/resuscitation fees. Information on shipping costs and any additional charges will be provided by the supplying MMRRC facility.

    Click button to Request this one strain. (Use the MMRRC Catalog Search to request more than one strain.)
    MMRRC Item # Description Distribution Fee / Unit (US $)
    *Shipping & Handling not included*
    Units Notes
    069938-UNC-RESUS Litter recovered from cryo-archive $2,914.00 / $4,837.00
    Non-Profit / For-Profit
    Litter Recovered litter4; additional fees for any special requests.
    Cryopreserved material may be available upon request, please inquire to mmrrc@med.unc.edu for more information.

    1 The distribution fee covers the expense of rederiving mice from a live mouse; you will receive the resulting litter. The litter will contain at minimum one mutant carrier; the actual number of animals and the gender and genotype ratios will vary. (Typically, multiple breeder pairs can be established from the recovered litter.) Prior to shipment, the MMRRC will provide information about the animals recovered. If you anticipate or find that you need to request specific genotypes, genders or quantities of mice in excess of what is likely from a resuscitated litter, you may discuss available options and pricing with the supplying MMRRC facility.

    2 An aliquot contains a sufficient number of embryos (in one or more vials or straws and based on the transfer success rate of the MMRRC facility) to transfer into one to three recipients. The MMRRC makes no guarantee concerning embryo transfer success experienced in the recipient investigator's laboratory. Neither gender nor genotype ratios are guaranteed.

    3 An aliquot is one straw or vial with sufficient sperm to recover at least one litter of mice, as per provided protocols, when performed at the MMRRC facility. The MMRRC makes no guarantee concerning the success of these procedures when performed outside the MMRRC facilities.

    4 The distribution fee covers the expense of resuscitating mice from the cryo-archive; you will receive the resulting litter. The litter will contain at minimum one mutant carrier; the actual number of animals and the gender and genotype ratios will vary. (Typically, multiple breeder pairs can be established from the recovered litter.) Prior to shipment, the MMRRC will provide information about the animals recovered. If you anticipate or find that you need to request specific genotypes, genders or quantities of mice in excess of what is likely from a resuscitated litter, you may discuss available options and pricing with the supplying MMRRC facility.

    To request material from the MMRRC: Please fill out our on-line request form (accessible from the catalog search results page, or click the Request this Strain button in the fees section). If you have questions or need assistance completing this form, you may call Customer Service at (800) 910-2291 (in USA or Canada) or (530) 757-5710 (international calls). Before you call, please have with you: the MMRRC item number, quantity needed, Bill-to and Ship-to contact information.