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Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

Abstract

The breast cancer resistance protein, also known as ABCG2, is one of the most highly studied ATP-binding cassette (ABC) transporters because of its ability to confer multidrug resistance1,2. The lack of information on the physiological role of ABCG2 in humans severely limits cancer chemotherapeutic approaches targeting this transporter. We report here that ABCG2 comprises the molecular basis of a new blood group system (Junior, Jr) and that individuals of the Jr(a−) blood type have inherited two null alleles of ABCG2. We identified five frameshift and three nonsense mutations in ABCG2. We also show that the prevalence of the Jr(a−) blood type in the Japanese and European Gypsy populations is related to the p.Gln126* and p.Arg236* protein alterations, respectively. The identification of ABCG2−/− (Jr(a−)) individuals who appear phenotypically normal is an essential step toward targeting ABCG2 in cancer and also in understanding the physiological and pharmacological roles of this promiscuous transporter in humans.

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Figure 1: The ABCG2 transporter encodes the Jra blood group antigen.
Figure 2: Null alleles of ABCG2 are responsible for the Jr(a−) blood type.

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References

  1. Polgar, O., Robey, R.W. & Bates, S.E. ABCG2: structure, function and role in drug response. Expert Opin. Drug Metab. Toxicol. 4, 1–15 (2008).

    Article  CAS  Google Scholar 

  2. Noguchi, K., Katayama, K., Mitsuhashi, J. & Sugimoto, Y. Functions of the breast cancer resistance protein (BCRP/ABCG2) in chemotherapy. Adv. Drug Deliv. Rev. 61, 26–33 (2009).

    Article  CAS  Google Scholar 

  3. Helias, V. et al. The human porphyrin transporter ABCB6 is dispensable for erythropoiesis but responsible for the new blood group system Langereis. Nat. Genet. published online, doi:10.1038/mg.1069 (15 January 2012).

  4. Kwon, M.Y., Su, L., Arndt, P.A., Garratty, G. & Blackall, D.P. Clinical significance of anti-Jra: report of two cases and review of the literature. Transfusion 44, 197–201 (2004).

    Article  Google Scholar 

  5. Peyrard, T. et al. Fatal hemolytic disease of the fetus and newborn associated with anti-Jr. Transfusion 48, 1906–1911 (2008).

    Article  Google Scholar 

  6. Nakajima, H. & Ito, K. An example of anti-Jra causing hemolytic disease of the newborn and frequency of Jra antigen in the Japanese population. Vox Sang. 35, 265–267 (1978).

    CAS  PubMed  Google Scholar 

  7. Miyazaki, T. et al. A human monoclonal antibody to high-frequency red cell antigen Jra. Vox Sang. 66, 51–54 (1994).

    CAS  PubMed  Google Scholar 

  8. Pisacka, M. et al. Six cases of anti-Jra antibody detected in one year—a probable relation with Gypsy ethnic minority from central Slovakia. Proceedings of the 26th Congress of the International Society for Blood Transfusion Vol. 78, 146 (Vienna, 2000).

  9. Scharenberg, C.W., Harkey, M.A. & Torok-Storb, B. The ABCG2 transporter is an efficient Hoechst 33342 efflux pump and is preferentially expressed by immature human hematopoietic progenitors. Blood 99, 507–512 (2002).

    Article  CAS  Google Scholar 

  10. Allikmets, R., Schriml, L.M., Hutchinson, A., Romano-Spica, V. & Dean, M. A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance. Cancer Res. 58, 5337–5339 (1998).

    CAS  PubMed  Google Scholar 

  11. Doyle, L.A. et al. A multidrug resistance transporter from human MCF-7 breast cancer cells. Proc. Natl. Acad. Sci. USA 95, 15665–15670 (1998).

    Article  CAS  Google Scholar 

  12. Miyake, K. et al. Molecular cloning of cDNAs which are highly overexpressed in mitoxantrone-resistant cells: demonstration of homology to ABC transport genes. Cancer Res. 59, 8–13 (1999).

    CAS  PubMed  Google Scholar 

  13. Vlaming, M.L., Lagas, J.S. & Schinkel, A.H. Physiological and pharmacological roles of ABCG2 (BCRP): recent findings in Abcg2 knockout mice. Adv. Drug Deliv. Rev. 61, 14–25 (2009).

    Article  CAS  Google Scholar 

  14. Maliepaard, M. et al. Subcellular localization and distribution of the breast cancer resistance protein transporter in normal human tissues. Cancer Res. 61, 3458–3464 (2001).

    CAS  PubMed  Google Scholar 

  15. Huls, M. et al. The breast cancer resistance protein transporter ABCG2 is expressed in the human kidney proximal tubule apical membrane. Kidney Int. 73, 220–225 (2008).

    Article  CAS  Google Scholar 

  16. Zhou, S. et al. Increased expression of the Abcg2 transporter during erythroid maturation plays a role in decreasing cellular protoporphyrin IX levels. Blood 105, 2571–2576 (2005).

    Article  CAS  Google Scholar 

  17. Cusatis, G. & Sparreboom, A. Pharmacogenomic importance of ABCG2. Pharmacogenomics 9, 1005–1009 (2008).

    Article  CAS  Google Scholar 

  18. Imai, Y. et al. C421A polymorphism in the human breast cancer resistance protein gene is associated with low expression of Q141K protein and low-level drug resistance. Mol. Cancer Ther. 1, 611–616 (2002).

    CAS  PubMed  Google Scholar 

  19. Lee, S.S. et al. Identification and functional assessment of BCRP polymorphisms in a Korean population. Drug Metab. Dispos. 35, 623–632 (2007).

    Article  CAS  Google Scholar 

  20. Kobayashi, D. et al. Functional assessment of ABCG2 (BCRP) gene polymorphisms to protein expression in human placenta. Drug Metab. Dispos. 33, 94–101 (2005).

    Article  CAS  Google Scholar 

  21. Tamura, A. et al. Re-evaluation and functional classification of non-synonymous single nucleotide polymorphisms of the human ATP-binding cassette transporter ABCG2. Cancer Sci. 98, 231–239 (2007).

    Article  CAS  Google Scholar 

  22. Dehghan, A. et al. Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. Lancet 372, 1953–1961 (2008).

    Article  CAS  Google Scholar 

  23. Kolz, M. et al. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet. 5, e1000504 (2009).

    Article  Google Scholar 

  24. Woodward, O.M. et al. Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Proc. Natl. Acad. Sci. USA 106, 10338–10342 (2009).

    Article  CAS  Google Scholar 

  25. Matsuo, H. et al. Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population. Sci. Transl. Med. 1, 5ra11 (2009).

    Article  Google Scholar 

  26. Jonker, J.W. et al. The breast cancer resistance protein protects against a major chlorophyll-derived dietary phototoxin and protoporphyria. Proc. Natl. Acad. Sci. USA 99, 15649–15654 (2002).

    Article  CAS  Google Scholar 

  27. Puy, H., Gouya, L. & Deybach, J.C. Porphyrias. Lancet 375, 924–937 (2010).

    Article  CAS  Google Scholar 

  28. Itoda, M. et al. Eight novel single nucleotide polymorphisms in ABCG2/BCRP in Japanese cancer patients administered irinotacan. Drug Metab. Pharmacokinet. 18, 212–217 (2003).

    Article  Google Scholar 

  29. Bäckstrom, G. et al. Genetic variation in the ATP-binding cassette transporter gene ABCG2 (BCRP) in a Swedish population. Eur. J. Pharm. Sci. 18, 359–364 (2003).

    Article  Google Scholar 

  30. Ballif, B.A., Carey, G.R., Sunyaev, S.R. & Gygi, S.P. Large-scale identification and evolution indexing of tyrosine phosphorylation sites from murine brain. J. Proteome Res. 7, 311–318 (2008).

    Article  CAS  Google Scholar 

  31. Elias, J.E. & Gygi, S.P. Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry. Nat. Methods 4, 207–214 (2007).

    Article  CAS  Google Scholar 

  32. Arnaud, L. et al. Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome. Transfusion 49, 479–484 (2009).

    Article  CAS  Google Scholar 

  33. Gouya, L. et al. Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria. Am. J. Hum. Genet. 78, 2–14 (2006).

    Article  CAS  Google Scholar 

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Acknowledgements

The authors are indebted to all present and past members of the CNRGS for identifying and conserving Jr(a−) blood samples and extracting genomic DNA. We greatly appreciate M. Le Gall for her thoughtful comments on the manuscript. This study was supported in part by the INTS, Inserm and Paris Diderot University (Paris 7). B.A.B. was funded by the Vermont Genetics Network through a grant from the US National Institutes of Health/National Center for Research Resources (P20 RR16462).

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Correspondence to Lionel Arnaud.

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Saison, C., Helias, V., Ballif, B. et al. Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior. Nat Genet 44, 174–177 (2012). https://doi.org/10.1038/ng.1070

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