C57BL/6JCya-Mtrf1lem1flox/Cya
Common Name:
Mtrf1l-flox
Product ID:
S-CKO-17830
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
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Basic Information
Strain Name
Mtrf1l-flox
Strain ID
CKOCMP-108853-Mtrf1l-B6J-VB
Gene Name
Product ID
S-CKO-17830
Gene Alias
9130004K12Rik
Background
C57BL/6JCya
NCBI ID
Modification
Conditional knockout
Chromosome
10
Phenotype
Document
Application
--
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Mtrf1lem1flox/Cya mice (Catalog S-CKO-17830) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000019908
NCBI RefSeq
NM_175374
Target Region
Exon 3
Size of Effective Region
~1.2 kb
Detailed Document
Overview of Gene Research
Mtrf1l, known as mitochondrial translational release factor 1 like, is a key mitochondrial translation factor. The mitochondrial translation process, where mitochondrial DNA-encoded genes are translated into proteins, is crucial for mitochondrial function, biogenesis, and integrity, and Mtrf1l is involved in the termination phase of this process [2,3]. It is among a series of factors that coordinate mitochondrial translation, which is essential for overall cellular energy production, metabolism, and other mitochondrial-related biological processes.
Muscle denervation in mice led to a decrease in the expression of Mtrf1l along with other mitochondrial translation factors, corresponding with a reduction in mitochondrial biogenesis [2]. In contrast, exercise training in mice upregulated Mtrf1l and other mitochondrial translation factors in the plantaris muscle, suggesting that Mtrf1l expression is related to mitochondrial biogenesis under different physiological conditions [3]. Also, in bovine oocytes, differences in Mtrf1l transcript levels were found between oocytes with greater and less developmental competence, indicating its potential role in oocyte development [1].
In conclusion, Mtrf1l is an important mitochondrial translation factor in the termination phase of mitochondrial translation, playing a role in processes such as mitochondrial biogenesis, as revealed by mouse models of muscle denervation and exercise, and potentially in oocyte development as shown in bovine studies. These findings contribute to our understanding of mitochondrial-related physiological processes and may have implications for understanding muscle-related and reproductive-related conditions.
References:
1. Nemcova, Lucie, Jansova, Denisa, Vodickova-Kepkova, Katerina, Machatkova, Marie, Kanka, Jiri. 2016. Detection of genes associated with developmental competence of bovine oocytes. In Animal reproduction science, 166, 58-71. doi:10.1016/j.anireprosci.2016.01.004. https://pubmed.ncbi.nlm.nih.gov/26811294/
2. Yokokawa, Takumi, Mori, Risako, Suga, Tadashi, Hayashi, Tatsuya, Fujita, Satoshi. 2020. Muscle denervation reduces mitochondrial biogenesis and mitochondrial translation factor expression in mice. In Biochemical and biophysical research communications, 527, 146-152. doi:10.1016/j.bbrc.2020.04.062. https://pubmed.ncbi.nlm.nih.gov/32446358/
3. Yokokawa, Takumi, Kido, Kohei, Suga, Tadashi, Hayashi, Tatsuya, Fujita, Satoshi. . Exercise-induced mitochondrial biogenesis coincides with the expression of mitochondrial translation factors in murine skeletal muscle. In Physiological reports, 6, e13893. doi:10.14814/phy2.13893. https://pubmed.ncbi.nlm.nih.gov/30369085/
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