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C57BL/6JCya-Myo19em1/Cya
Common Name:
Myo19-KO
Product ID:
S-KO-11582
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Myo19-KO
Strain ID
KOCMP-66196-Myo19-B6J-VA
Gene Name
Myo19
Product ID
S-KO-11582
Gene Alias
1110055A02Rik; Myohd1
Background
C57BL/6JCya
NCBI ID
66196
Modification
Conventional knockout
Chromosome
11
Phenotype
MGI:1913446
Document
Click here to download >>
Application
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Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Myo19em1/Cya mice (Catalog S-KO-11582) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000093969
NCBI RefSeq
NM_025414
Target Region
Exon 3~22
Size of Effective Region
~23.0 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Myo19, a mitochondrially localized myosin, is crucial for mitochondrial homeostasis as it promotes mitochondrial fission by tethering mitochondria to endoplasmic reticulum-associated actin [1]. It is also involved in mitochondrial movement, dynamics, and positioning, and impacts cell function through its effects on mitochondria [2,3]. Myo19 has a unique evolutionary history and is an actin-activated ATPase [2].

Myo19 knockdown led to mitochondrial elongation, while overexpression induced fragmentation [1]. In Myo19-deficient HEK293T cells, mitochondria were not properly fragmented at mitosis, and were partitioned asymmetrically to daughter cells. Respiratory functions were impaired, ROS generation was enhanced, and cell proliferation, cytokinesis, and cell-matrix adhesion were negatively affected [5]. Myo19 silencing in cells also caused defects in mitochondrial distribution within cells and during division, and some cells underwent stochastic division failure [6]. Loss of Myo19 enhanced the microenvironmental ROS gradient, promoting tumor cell chemotaxis and metastasis [4].

In conclusion, Myo19 is essential for maintaining mitochondrial dynamics, including fission, and for proper mitochondrial inheritance during cell division. Its loss is associated with abnormal mitochondrial functions and increased tumor metastasis, highlighting its significance in normal cellular processes and disease, especially in understanding the role of mitochondria in cancer metastasis.

References:

1. Coscia, Stephen M, Thompson, Cameron P, Tang, Qing, Lakadamyali, Melike, Holzbaur, Erika L F. 2023. Myo19 tethers mitochondria to endoplasmic reticulum-associated actin to promote mitochondrial fission. In Journal of cell science, 136, . doi:10.1242/jcs.260612. https://pubmed.ncbi.nlm.nih.gov/36744380/

2. Bocanegra, Jennifer L, Adikes, Rebecca, Quintero, Omar A. . Myosin XIX. In Advances in experimental medicine and biology, 1239, 439-451. doi:10.1007/978-3-030-38062-5_20. https://pubmed.ncbi.nlm.nih.gov/32451871/

3. Shneyer, Boris I, Ušaj, Marko, Henn, Arnon. 2015. Myo19 is an outer mitochondrial membrane motor and effector of starvation-induced filopodia. In Journal of cell science, 129, 543-56. doi:10.1242/jcs.175349. https://pubmed.ncbi.nlm.nih.gov/26659663/

4. Ren, Xiaoyu, Shi, Peng, Su, Jing, Hu, Yiping, Wu, Congying. 2024. Loss of Myo19 increases metastasis by enhancing microenvironmental ROS gradient and chemotaxis. In EMBO reports, 25, 971-990. doi:10.1038/s44319-023-00052-y. https://pubmed.ncbi.nlm.nih.gov/38279020/

5. Majstrowicz, Katarzyna, Honnert, Ulrike, Nikolaus, Petra, Hemkemeyer, Sandra A, Bähler, Martin. 2021. Coordination of mitochondrial and cellular dynamics by the actin-based motor Myo19. In Journal of cell science, 134, . doi:10.1242/jcs.255844. https://pubmed.ncbi.nlm.nih.gov/34013964/

6. Rohn, Jennifer L, Patel, Jigna V, Neumann, Beate, Ellenberg, Jan, Baum, Buzz. 2014. Myo19 ensures symmetric partitioning of mitochondria and coupling of mitochondrial segregation to cell division. In Current biology : CB, 24, 2598-605. doi:10.1016/j.cub.2014.09.045. https://pubmed.ncbi.nlm.nih.gov/25447992/

Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
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