Table 1

Selected properties of individual murine NFATc proteins expressed in lymphoid cells
NFATc Proteins Length1) Induction2) SUMO- Properties Refs.
[aa] RNA/Protein sites3)
NFATc1/αA 717 +/+++ (1) anti-apoptotic, supports proliferation, anti-anergic, oncogenic activity [24,38,39,90]
(NFATc,
NFAT2)
NFATc1/βA 703 -/- (1) n.d. [38]
NFATc1/αC 939 +/+/- 2 (+1) pro-apoptotic, (inhibits proliferation) [35,38,39]
NFATc1/βC 925 -/- 2 (+1) n.d. [38]
NFATc2 923-927 (+)/- 2 pro-apoptotic, anti-proliferative, supports anergy induction, tumor suppressor activity [24,35,56,57,59,90,97,98]
(NFAT1)
NFATc3 1076 /- 1-2 (anti-proliferative) [98]
(NFAT4,
NFATx)

1) Data from the NCBI database “Gene”. There, two short NFATc2 versions of 452 and 672 aa are also documented. However, their expression and function are unknown. For a comprehensive study about human and murine NFATc RNAs see Ref. [47].

2) Induction upon immune receptor stimulation in naïve and Th0/Th1 effector T cells and splenic B cells. RNA data were compiled from RNA Seq (E.S. et al., unpubl.) and real time PCR data obtained with splenic T and B cells upon primary stimulation [39]. The protein data reflect the results of Western blot assays [39]. +, 3–5 fold induction; +++, 50 fold induction and more.

3) Existence of SUMO-consensus sites within NFATc proteins. For NFATc1 and c2, their SUMOylation has been demonstrated in vivo[38,97]. (1) for NFATc1 indicates the existence of a “silent” SUMO consensus sites which remains un-used [38]. In NFATc3, two SUMO sites are present but only one corresponds to a “perfect” site.

Serfling et al. Cell Communication and Signaling 2012 10:16   doi:10.1186/1478-811X-10-16

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