KC-5675

HCT116-WRN-1577-1G>C-KI Cell Line

58505

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Background of HCT116-WRN-1577-1G>C-KI Cell Line

The WRN gene encodes a member of the RecQ helicase family, which plays a critical role in maintaining genomic stability through its involvement in DNA repair, replication, recombination, and telomere maintenance. Mutations in WRN are associated with Werner syndrome (WS), a rare autosomal recessive disorder characterized by premature aging, genomic instability, and increased cancer susceptibility. The WRN protein possesses 3′→5′ helicase and 3′→5′ exonuclease activities, both of which are essential for its function in DNA metabolism. Given its importance in preserving genomic integrity, understanding the functional consequences of WRN mutations is crucial for elucidating the molecular mechanisms underlying WS and related disorders.

Specifications

Catalog Number	KC-5675
Cell Line Name	HCT116-WRN-1577-1G>C-KI Cell Line
Clone Number	2B4
Host Cell Line	HCT116
Description	Stable HCT116 clone expressing endogenous WRN gene bearing c.1577-1G>C mutation.
Quantity	Two vials of frozen cells (≥2-10⁶/vial)
Stability	Stable in culture over a minimum of 10 passages
Application	Drug screening and biological assays
Freezing Medium	70% RPMI1640 + 20% FBS + 10% DMSO
Propagation Medium	RPMI1640 + 10% FBS
Selection Marker	NA
Morphology	Fibroblastoid cells growing as a monolayer
Subculture	Split the saturated culture at a ratio of 1:4-1:5 every 2-3 days; seed out at about 1-3 x 10⁵ cells/mL
Incubation	37 °C with 5% CO₂
Storage	Liquid nitrogen immediately upon receiving
Doubling Time	Approximately 30 hours
Mycoplasma Status	Negative

Cell Line Generation

HCT116-WRN-1577-1G>C-KI cell line was generated using the CRISPR method.

Characterization

Figure 1: Characterization of HCT116-WRN-1577-1G>C-KI Cell Line stable clone using PCR sequencing.

Figure 2: Characterization of Dose-response curves and IC50 values for HCT116 and HCT116-WRN-1577-1G>C-KI cells treated with VVD-214 and HRO761 over 5 days.

Cell Resuscitation

Prewarm culture medium (RPMI1640+10% FBS)in a 37°C water bath.
Thaw the frozen vial in a 37°C water bath for 1-2 minutes.
Transfer the vial into biosafety cabinet, and wipe the surface with 70% ethanol.
Unscrew the top of the vial and transfer the cell suspension gently into a sterile centrifuge tube containing 9.0mL complete culture medium.
Spin at ~ 125 × g for 5-7 minutes at room temperature, and discard the supernatant without disturbing the pellet.
Resuspend cell pellet with the appropriate volume of complete medium and transfer the cell suspension into a T25 culture flask.
Incubate the flask at 37°C, 5% CO₂ incubator.
Split saturated culture 1:4-1:5 every 2-3 days; seed out at about 1-3 × 10⁵ cells/mL.

Cell Freezing

Prepare the freezing medium (70% RPMI1640 + 20% FBS + 10% DMSO) fresh immediately before use.
Keep the freezing medium on ice and label cryovials.
Transfer cells to a sterile, conical centrifuge tube, and count the cells.
Centrifuge the cells at 250×g for 5 minutes at room temperature and carefully aspirate off the medium.
Resuspend the cells at a density of at least 3×10⁶ cells/mL in chilled freezing medium.
Aliquot 1 mL of the cell suspension into each cryovial.
Freeze cells in the CoolCell freezing container overnight in a -80°C freezer.
Transfer vials to liquid nitrogen for long-term storage.

References

Croteau DL, Popuri V, Opresko PL, Bohr VA. (2014). Human RecQ helicases in DNA repair, recombination, and replication. Annu Rev Biochem, 83, 519-52. PMID: 24606147.
Oshima J, Sidorova JM, Monnat RJ Jr. (2017). Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions. Ageing Res Rev, 33, 105-114. PMID: 27312357.
Huang S, Li B, Gray MD, Oshima J, Mian IS, Campisi J. (2006). The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease. Nat Genet, 20(2), 114-6. PMID: 9771702.