Mutation Reduces Immune Response in C57BL/6J Mice

Philip Dubé, PhD
Tuesday, February 14th, 2017
Researchers from the University of Iowa inadvertently identified an Nlrp12 missense mutation which inhibits immune responses in C57BL/6J mice. Further investigation reveals the mutation occurred prior to 1971, potentially impacting decades of research conducted on affected mouse models.

Reduced Neutrophil Recruitment in C57BL/6J

In this study, the authors compared C57BL/6J and C57BL/6NTac mice and noted that C57BL/6J mice had reduced neutrophil recruitment. Initially hypothesizing the difference was due to a microbiome effect, possibly segmented filamentous bacteria (SFB), they found that this deficit had a genetic basis and was linked to a previously identified single nucleotide polymorphism (SNP) in the Nlrp12 gene.

They showed that the C57BL/6J missense mutation was dominant and that the associated neutrophil defect was phenocopied in Nlrp12-/- mice on either the C57BL/6N or BALB/c backgrounds.

Related InsightRead the Taconic Biosciences' Insight:

How is the Immune Response in C57BL/6J Affected?

NLRP12 (Nod-like receptor pyrin domain containing 12) is a component of the innate immune system that regulates immune cell trafficking and cytokine production. The C57BL/6J mutation (G to A at position 3,222,537, Chr. 7) causes an amino acid substitution in NLRP12 (arginine to lysine at residue 1034) in a conserved leucine rich repeat (LRR) domain which is putatively important for protein-protein interactions.

The affected LRR domain from NLRP12 is highly conserved among mammals. There are two important exceptions within the Mus genus:

  1. lysine (K) to arginine (R) substitution at position 1034
  2. methionine (M)/valine (V) to lysine (K) substitution at position 1035
Figure 1: Multiple sequence alignment of NLRP12
(LRR 8 domain)
Essentially, the lysine at position 1034 in this domain is shifted by one residue within the Mus genus. It is notable that the subsequent C57BL/6J mutation introduced a double lysine residue in this domain which is unique among all mammals. A double lysine within this highly-conserved domain may potentially affect protein-protein interactions or the post-translational regulation of NLRP12.

It is unclear how either of the mouse NLRP12 variants functionally compare to human NLRP12; however, these new data show that the C57BL/6J Nlrp12 variant is a loss-of-function mutation as compared to Nlrp12 from other mouse strains (including C57BL/6N and BALB/c).

When Did This Mutation Occur?

The mutation is specific to C57BL/6J and related substrains, and is not present in C57BL/6N strains. This suggests that the C57BL/6J mutation arose after the separation of the C57BL/6J and C57BL/6N substrains in 1951.

Our data show that a related C57BL/6J substrain, C57BL/6JBomTac, also carries this mutation, indicating that this mutation arose prior to 1971 when this substrain separated from the ancestral C57BL/6J.

Moreover, sequence data from 3 wild-sourced mouse lines and 16 inbred strains show that the C57BL/6J variant is unique in the Mus genus. These findings emphasize the importance of indicating the full designation of mice used in studies or in the creation of genetically modified mouse models.

Many of the most popular C57BL/6 embryonic stem (ES) cells were derived from a C57BL/6NTac mouse, including JM8 and all derivatives, C2, B6/BLU and VGB6. These are the cells of choice for many cutting-edge genome projects, including the Knockout Mouse Project (KOMP) and the International Mouse Phenotyping Consortium (IMPC). Taconic Model Generation Solutions uses highly germline competent C57BL/6NTac ES cells to create genetically modified mice.

Documenting C57BL/6 Substrains

There are at least 16 different C57BL/6 substrains that have diverged since the original isolation of this line in the 1930s. There are numerous genetic differences between the two main C57BL/6 branches (C57BL/6J and C57BL/6N). Furthermore, substrains within each of these two branches, as maintained by different vendors, are distinct and each carries a unique spectrum of genetic characteristics.

Given this diversity, it is important that researchers understand and appropriately document the specific inbred stain/substrain/source used in studies. The literature is full of instances of incomplete details regarding the specifics or sources of "C57BL/6" mice - this could refer to any one of at least 16 different inbred strains with different genetic profiles!

These new findings emphasize the importance of completely indicating the full designation of mice used in studies, and in the creation or maintenance of genetically modified mice. Examples of a full designation for a C57BL/6 inbred strain would include: C57BL/6NTac or C57BL/6JBomTac.

Figure 2: Sequencing data confirm that the C57BL/6J mutation is absent in the C57BL/6NTac strain, but is present in the C57BL/6JBomTac strain (Departments of Genetic Sciences and Compliance, and Molecular Analysis, Taconic Biosciences)

Taconic Mouse Models Taconic Biosciences' Quality Information
Ulland TK, Jain N, Hornick EE, Elliott EI, Clay GM, Sadler JJ, Mills KA, Janowski AM, Volk AP, Wang K, Legge KL, Gakhar L, Bourdi M, Ferguson PJ, Wilson ME, Cassel SL, Sutterwala FS. Nlrp12 mutation causes C57BL/6J strain-specific defect in neutrophil recruitment. Nat Commun. 2016 Oct 25;7:13180.
Simon MM, Greenaway S, White JK, et al. A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 2013 Jul 31;14(7):R82.
Arthur JC, Lich JD, Ye Z, Allen IC, Gris D, Wilson JE, Schneider M, Roney KE, O'Connor BP, Moore CB, Morrison A, Sutterwala FS, Bertin J, Koller BH, Liu Z, Ting JP. Cutting edge: NLRP12 controls dendritic and myeloid cell migration to affect contact hypersensitivity. J Immunol. 2010 Oct 15;185(8):4515-9.
Lukens JR, Gurung P, Shaw PJ, Barr MJ, Zaki MH, Brown SA, Vogel P, Chi H, Kanneganti TD. The NLRP12 Sensor Negatively Regulates Autoinflammatory Disease by Modulating Interleukin-4 Production in T Cells. Immunity. 2015 Apr 21;42(4):654-64.
Simon MM, Greenaway S, White JK, et al. A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 2013 Jul 31;14(7):R82.
Zurita E, Chagoyen M, Cantero M, Alonso R, González-Neira A, López-Jiménez A, López-Moreno JA, Landel CP, Benítez J, Pazos F, Montoliu L. Genetic polymorphisms among C57BL/6 mouse inbred strains. Transgenic Res. 2011 Jun;20(3):481-9.

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