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C57BL/6JCya-Rab10em1/Cya
Common Name:
Rab10-KO
Product ID:
S-KO-18769
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Rab10-KO
Strain ID
KOCMP-19325-Rab10-B6J-VA
Gene Name
Rab10
Product ID
S-KO-18769
Gene Alias
-
Background
C57BL/6JCya
NCBI ID
19325
Modification
Conventional knockout
Chromosome
12
Phenotype
MGI:105066
Document
Click here to download >>
Application
--
More
Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Rab10em1/Cya mice (Catalog S-KO-18769) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000021001
NCBI RefSeq
NM_016676
Target Region
Exon 3
Size of Effective Region
~1.0 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Rab10, a member of the small GTPase family, is involved in multiple cellular trafficking processes. It plays a role in the formation of recycling endosomal compartments like tubular endosomes through interaction with kinesin motors KIF13A and KIF13B [10]. Rab10 is also associated with pathways related to cell migration, lysosomal function, and is implicated in several disease conditions, making it a potential biomarker or drug target.

In Alzheimer's disease, a rare variant in the 3'-UTR of RAB10 has been identified as protective, indicating its possible role in disease resilience [2]. In Parkinson's disease, genetic variation at the LRRK2 locus, which can phosphorylate Rab10, is linked to disease risk. Lysosomal positioning regulates Rab10 phosphorylation by LRRK2, and loss of VPS13C, associated with early-onset Parkinson's disease, disrupts phospho-Rab10-mediated lysosomal function [4,5]. Also, urinary Rab10 phosphorylation is elevated in idiopathic Parkinson disease and is associated with disease progression [7]. In hepatocellular carcinoma, O-GlcNAcylation of RAB10 by OGT stabilizes it, accelerating cancer progression [3]. In breast cancer, RAB10 expression is elevated, promoting cell proliferation, migration, and invasion, and predicting a poor prognosis [9]. Moreover, Rab10-CAV1 mediated intraluminal vesicle transport to migrasomes is important for intercellular communication during skin wound healing [1]. Heterozygous Rab10 knock-out mice show changes in pathways related to neuronal metabolism, inflammation, and aging, and perform differently in hippocampal-dependent tasks, suggesting Rab10's role in controlling brain circuitry [6]. Rab10 also regulates lysosome exocytosis and plasma membrane repair [8].

In conclusion, Rab10 is crucial for multiple cellular functions such as endosomal formation, vesicle transport, and lysosomal function. Studies using gene knockout mouse models have revealed its significant roles in neurodegenerative diseases like Alzheimer's and Parkinson's, as well as in cancer. Understanding Rab10's functions provides insights into disease mechanisms and potential therapeutic targets.

References:
1. Li, Yong, Wen, Yiling, Li, Ying, Wong, Catherine C L, Chen, Yang. 2024. Rab10-CAV1 mediated intraluminal vesicle transport to migrasomes. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2319267121. doi:10.1073/pnas.2319267121. https://pubmed.ncbi.nlm.nih.gov/39008679/
2. Tavana, Justina P, Rosene, Matthew, Jensen, Nick O, Kauwe, John Sk, Karch, Celeste M. 2018. RAB10: an Alzheimer's disease resilience locus and potential drug target. In Clinical interventions in aging, 14, 73-79. doi:10.2147/CIA.S159148. https://pubmed.ncbi.nlm.nih.gov/30643396/
3. Lv, Zhuo, Ma, Guolu, Zhong, Zhuo, Li, Bin, Long, De. . O-GlcNAcylation of RAB10 promotes hepatocellular carcinoma progression. In Carcinogenesis, 44, 785-794. doi:10.1093/carcin/bgad034. https://pubmed.ncbi.nlm.nih.gov/37218374/
4. Kluss, Jillian H, Beilina, Alexandra, Williamson, Chad D, Cookson, Mark R, Bonet-Ponce, Luis. 2022. Lysosomal positioning regulates Rab10 phosphorylation at LRRK2+ lysosomes. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2205492119. doi:10.1073/pnas.2205492119. https://pubmed.ncbi.nlm.nih.gov/36256825/
5. Schrӧder, Leonie F, Peng, Wesley, Gao, Ge, Schwake, Michael, Krainc, Dimitri. 2024. VPS13C regulates phospho-Rab10-mediated lysosomal function in human dopaminergic neurons. In The Journal of cell biology, 223, . doi:10.1083/jcb.202304042. https://pubmed.ncbi.nlm.nih.gov/38358348/
6. Bunner, Wyatt, Wang, Jie, Cohen, Sarah, Yasuda, Ryohei, Szatmari, Erzsebet M. 2023. Behavioral and Transcriptome Profiling of Heterozygous Rab10 Knock-Out Mice. In eNeuro, 10, . doi:10.1523/ENEURO.0459-22.2023. https://pubmed.ncbi.nlm.nih.gov/37156612/
7. Wang, Shijie, Unnithan, Shakthi, Bryant, Nicole, Al-Khalidi, Hussein R, West, Andrew B. 2022. Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. In Movement disorders : official journal of the Movement Disorder Society, 37, 1454-1464. doi:10.1002/mds.29043. https://pubmed.ncbi.nlm.nih.gov/35521944/
8. Vieira, Otilia V. 2016. Rab3a and Rab10 are regulators of lysosome exocytosis and plasma membrane repair. In Small GTPases, 9, 349-351. doi:10.1080/21541248.2016.1235004. https://pubmed.ncbi.nlm.nih.gov/27687479/
9. Zhuo, Jian, Han, Jianjun, Zhao, Yanchun, Yang, Xiaohong, Liu, Weiguang. 2023. RAB10 promotes breast cancer proliferation migration and invasion predicting a poor prognosis for breast cancer. In Scientific reports, 13, 15252. doi:10.1038/s41598-023-42434-1. https://pubmed.ncbi.nlm.nih.gov/37709911/
10. Etoh, Kan, Fukuda, Mitsunori. 2019. Rab10 regulates tubular endosome formation through KIF13A and KIF13B motors. In Journal of cell science, 132, . doi:10.1242/jcs.226977. https://pubmed.ncbi.nlm.nih.gov/30700496/
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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