Structure-function Studies in Mouse Embryonic Stem Cells Using Recombinase-mediated Cassette Exchange

Summary

Proteins often contain multiple domains that can exert different cellular functions. Gene knock-outs (KO) do not consider this functional diversity. Here, we report a recombination-mediated cassette exchange (RMCE)-based structure-function approach in KO embryonic stem cells that allows for the molecular dissection of various functional domains or variants of a protein.

Abstract

Gene engineering in mouse embryos or embryonic stem cells (mESCs) allows for the study of the function of a given protein. Proteins are the workhorses of the cell and often consist of multiple functional domains, which can be influenced by posttranslational modifications. The depletion of the entire protein in conditional or constitutive knock-out (KO) mice does not take into account this functional diversity and regulation. An mESC line and a derived mouse model, in which a docking site for FLPe recombination-mediated cassette exchange (RMCE) was inserted within the ROSA26 (R26) locus, was previously reported. Here, we report on a structure-function approach that allows for molecular dissection of the different functionalities of a multidomain protein. To this end, RMCE-compatible mice must be crossed with KO mice and then RMCE-compatible KO mESCs must be isolated. Next, a panel of putative rescue constructs can be introduced into the R26 locus via RMCE targeting. The candidate rescue cDNAs can be easily inserted between RMCE sites of the targeting vector using recombination cloning. Next, KO mESCs are transfected with the targeting vector in combination with an FLPe recombinase expression plasmid. RMCE reactivates the promoter-less neomycin-resistance gene in the ROSA26 docking sites and allows for the selection of the correct targeting event. In this way, high targeting efficiencies close to 100% are obtained, allowing for insertion of multiple putative rescue constructs in a semi-high throughput manner. Finally, a multitude of R26-driven rescue constructs can be tested for their ability to rescue the phenotype that was observed in parental KO mESCs. We present a proof-of-principle structure-function study in p120 catenin (p120ctn) KO mESCs using endoderm differentiation in embryoid bodies (EBs) as the phenotypic readout. This approach enables the identification of important domains, putative downstream pathways, and disease-relevant point mutations that underlie KO phenotypes for a given protein.

Introduction

It is estimated that mammalian genomes contain about 20,000 protein-coding genes. Alternative splicing and posttranslational modifications further increase the protein repertoire. Proteins have a modular structure¹ and often contain multiple interaction domains, which allow their recruitment into different protein complexes and their participation in multiple cellular processes². One example is the multi-functional protein called p120ctn. p120ctn is encoded by the Ctnnd1 gene and consists of a large central armadillo repeat domain flanked by an N-terminal and a C-terminal region. The armadillo domain of p120ctn ....

Protocol

All experiments on mice were conducted according to institutional, national, and European animal regulations.

1. Isolation of RMCE-compatible KO mESCs

1. Breed heterozygous KO mice with RMCE-compatible mice, such as ROSALUC mice¹⁰ or ROSA26-iPSC mice²¹. Both RMCE-compatible mice were maintained on a mixed 129/C57BL6/Swiss background.
   NOTE: Crossing with heterozygous KO mice is advised to overcome embryonic lethality in homozygous KO mice.
2. Use PCR to select heterozygous KO mice containing an RMCE cassette in the R26 locus¹².
3. Breed RMCE-compatible, heterozygo....

Results

The procedure to isolate RMCE-compatible KO mESC lines is depicted in Figure 2. Two consecutive breedings are required to obtain RMCE-compatible KO blastocysts. First, heterozygous KO mice are crossed with RMCE-compatible mice to obtain RMCE-compatible, heterozygous KO mice. These mice are then used for timed matings with other heterozygous KO mice to obtain 3.5-dpc, RMCE-compatible, homozygous KO blastocysts. The chance of obtaining such an embryo is one in eight, as pre.......

Discussion

Our mESC isolation method is user-friendly and does not require advanced skills or equipment, such as microsurgery of blastocysts. Thus, this technology is accessible to a large proportion of the scientific community. Anyone with basic cell culture experience can propagate ICM outgrowths and establish mESCs lines. However, the flushing and handling of blastocysts requires some practice. A mouth pipette is used to transfer blastocysts and consists of a micropipette, a micropipette holder, tubing, and an aspirator mouthpie.......

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
ROSALUC Mice	made in house		frozen sperm available upon request
R26-iPSC mice	made in house		frozen sperm available upon request
Vessel probe	Fine Science Tools	10160-13	to check for copulation plugs
M2 medium	Sigma-Aldrich	M7167	make aliquots and store at -20 °C
Fine forceps (Dumont #5 Standard tip Student forceps)	Fine Science Tools	11251-10	spray with 70% EtOH before use (do not autoclave)
23 G needles	Fine-ject	8697
1-mL syringes	Soft-ject	6680
60-mm bacterial grade plates (for flushing)	Gosselin	BB60-01
Mouth pipette	made in house		see discussion
Mouse embryonic fibroblasts (MEFs, TgN (DR4)1 Jae strain)	ATTC	SCRC-1045
TgN (DR4)1 Jae mice	The Jackson Laboratory	3208
Mitomycin C	Sigma-Aldrich	M0503
Phosphate buffered saline (PBS) without calcium or magnesium	Gibco	14190-094
Tg(DR4)1Jae/J mice	JAX	3208	mice that contain four drug-selectable genes and DR4 MEFS confers resistance to neomycin, puromycin, hygromycin and 6-thioguanine
0.1% Gelatin	Sigma-Aldrich	G1393	Dissolve 0.5 g in 500 mL distilled water, autoclave and store at 4 °C.
Trypsin (0.25%)	Gibco	25200-056
2 μM pluripotin	Cayman Chemical	10009557
pRMCE-DV1	BCCM/LMBP collection	LMBP 08870	public available from the BCCM/LMBP collection (http://bccm.belspo.be)
cre-excised pRMCE-DV1	BCCM/LMBP collection	LMBP 08195	public available from the BCCM/LMBP collection (http://bccm.belspo.be)
pCAG-FlpE-IRES-Puro-pA	Addgene	20733
heat-shock competent DH5α bacteria	made in house
Gateway pDONR221 vector	Thermo Fisher	12536-017	contains kanamycin-resistance gene
BP clonase II mix	Thermo Fisher	11789-020
LR clonase II mix	Thermo Fisher	11791-020
Luria Broth (LB)
Ampicillin
Applied Biosystems 3730XL DNA Analyzer	Thermo Fisher	3730XL
G418	Thermo Fisher	11811-023
Lipofectamine 2000 transfection reagent	Thermo Fisher	11668027
Lipofectamine LTX transfection reagent	Thermo Fisher	15338100
Effectene transfection reagent	Qiagen	301425
GATEWAY pENTR 1A vector	Thermo Fisher	A10462	recombination-compatible vector
mouse monoclonal anti-p120ctn antibody	BD Transduction Laboratories	610134
mouse monoclonal anti-Ecadherin antibody	BD Transduction Laboratories	610181
General equipment
Sterile dissection tools			fine scissors and forceps for dissecting the uterus
Sterile pipettes: 5 mL, 10 mL and 25 mL
15-mL and 50-mL conical centrifuge tubes
96-well culture plates V-shaped bottom and flat bottom)
Culture dishes: 24 wells, 12 wells and 6 wells
Multichannel pipettes (to pipette 30, 50, 100 and 200 μL)
Sterile multichannel reservoirs
Access to a laminar air flow
Access to an incubator at 37 °C with 5% CO2
Access to an inverted microscope
Access to a bench-top centrifuge
Access to a stereo microscope with transmitted-light
Culture media
MEF Medium			stored at 4 °C; warm 30 min at 37 °C before use
Dulbecco’s modified Eagle’s medium (DMEM)	Gibco	41965-062
10% fetal bovine serum (FBS)	Sigma-Aldrich	F-7524
L-glutamine (2 mM)	Gibco	25030-024
Sodium pyruvate  (0.4 mM)	Gibco	11360-039
penicillin (100 U/mL)	Gibco	15140-122
streptomycin (100 µg/mL)	Gibco	15140-122
SR-based mESC medium			stored at 4 °C; warm 30 min at 37 °C before use
DMEM/F12	Gibco	31330-038	mixed in a 1:1 ratio
15% knock-out serum replacement (SR)	Gibco	10828–028
L-glutamine (2 mM)	Gibco	25030-024
0.1 mM non-essential amino acids	Gibco	11140-050
penicillin (100 U/mL)	Gibco	15140-122
streptomycin (100 µg/mL)	Gibco	15140-122
β-mercaptoethanol (0.1 mM)	Sigma-Aldrich	M 3148
2,000 U/mL recombinant mouse LIF	(IRC/VIB Protein Service facility)
FBS-based mESC medium (similar to SR-based mESC medium)			stored at 4°C; warm 30 min at 37°C before use
Knockout DMEM	Gibco	10829-018
15% FBS	Hyclone	SH30070.03E
Differention Medium			stored at 4 °C; warm 30 min at 37 °C before use
Iscove's Modified Dulbecco's Medium (IMDM)	Gibco	21980-032
15% FBS	Hyclone	SH30070.03E
5% CD Hybridoma Medium(1x) liquid	Gibco	11279-023
2 mM L-glutamine	Gibco	25030-024
0.4 mM 1-thioglycerol	Sigma-Aldrich	M-6145
50 μg/mL ascorbic acid	Sigma-Aldrich	A-4544
penicillin (100 U/mL)	Gibco	15140-122
streptomycin (100 µg/mL)	Gibco	15140-122
2i
1 μM Erk inhibitor PD0325901	Axon Medchem	Axon 1408
3 μM Gsk3 inhibitor CHIR99021	Axon Medchem	Axon 1386