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Anemia
Volume 2012, Article ID 926787, 10 pages
http://dx.doi.org/10.1155/2012/926787
Review Article

Towards a Molecular Understanding of the Fanconi Anemia Core Complex

Protein Structure and Function Laboratory, Lincoln's Inn Fields Laboratories, London Research Institute, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 3LY, UK

Received 15 December 2011; Accepted 21 March 2012

Academic Editor: Stefan Meyer

Copyright © 2012 Charlotte Hodson and Helen Walden. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. B. P. Alter, “Fanconi's anemia and malignancies,” American Journal of Hematology, vol. 53, no. 2, pp. 99–110, 1996. View at Google Scholar
  2. J. German, S. Schonberg, and S. Caskie, “A test for Fanconi's anemia,” Blood, vol. 69, no. 6, pp. 1637–1641, 1987. View at Google Scholar · View at Scopus
  3. A. R. Meetei, A. L. Medhurst, C. Ling et al., “A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M,” Nature Genetics, vol. 37, no. 9, pp. 958–963, 2005. View at Publisher · View at Google Scholar · View at Scopus
  4. A. Smogorzewska, S. Matsuoka, P. Vinciguerra et al., “Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair,” Cell, vol. 129, no. 2, pp. 289–301, 2007. View at Publisher · View at Google Scholar · View at Scopus
  5. A. E. Sims, E. Spiteri, R. J. Sims et al., “FANCI is a second monoubiquitinated member of the Fanconi anemia pathway,” Nature Structural and Molecular Biology, vol. 14, no. 6, pp. 564–567, 2007. View at Publisher · View at Google Scholar · View at Scopus
  6. C. Timmers, T. Taniguchi, J. Hejna et al., “Positional cloning of a novel Fanconi anemia gene, FANCD2,” Molecular Cell, vol. 7, no. 2, pp. 241–248, 2001. View at Publisher · View at Google Scholar · View at Scopus
  7. I. Garcia-Higuera, T. Taniguchi, S. Ganesan et al., “Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway,” Molecular Cell, vol. 7, no. 2, pp. 249–262, 2001. View at Publisher · View at Google Scholar · View at Scopus
  8. A. R. Meetei, J. P. de Winter, A. L. Medhurst et al., “A novel ubiquitin ligase is deficient in Fanconi anemia,” Nature Genetics, vol. 35, no. 2, pp. 165–170, 2003. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Levitus, Q. Waisfisz, B. C. Godthelp et al., “The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J,” Nature Genetics, vol. 37, no. 9, pp. 934–935, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. N. G. Howlett, T. Taniguchi, S. Olson et al., “Biallelic inactivation of BRCA2 in Fanconi anemia,” Science, vol. 297, no. 5581, pp. 606–609, 2002. View at Publisher · View at Google Scholar · View at Scopus
  11. J. P. de Winter, Q. Waisfisz, M. A. Rooimans et al., “The Fanconi anaemia group G gene FANCG is identical with XRCC9,” Nature Genetics, vol. 20, no. 3, pp. 281–283, 1998. View at Publisher · View at Google Scholar · View at Scopus
  12. J. P. de Winter, M. A. Rooimans, L. van der Weel et al., “The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM,” Nature Genetics, vol. 24, no. 1, pp. 15–16, 2000. View at Publisher · View at Google Scholar · View at Scopus
  13. A. R. Meetei, M. Levitus, Y. Xue et al., “X-linked inheritance of Fanconi anemia complementation group B,” Nature Genetics, vol. 36, no. 11, pp. 1219–1224, 2004. View at Publisher · View at Google Scholar · View at Scopus
  14. J. R. L. T. Foe, M. A. Rooimans, L. Bosnoyan-Collins et al., “Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA,” Nature Genetics, vol. 14, no. 3, pp. 320–323, 1996. View at Google Scholar · View at Scopus
  15. C. A. Strathdee, A. M. V. Duncan, and M. Buchwald, “Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9,” Nature Genetics, vol. 1, no. 3, pp. 196–198, 1992. View at Google Scholar · View at Scopus
  16. M. Levitus, M. A. Rooimans, J. Steltenpool et al., “Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes,” Blood, vol. 103, no. 7, pp. 2498–2503, 2004. View at Publisher · View at Google Scholar · View at Scopus
  17. O. Levran, C. Attwooll, R. T. Henry et al., “The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia,” Nature Genetics, vol. 37, no. 9, pp. 931–933, 2005. View at Publisher · View at Google Scholar · View at Scopus
  18. R. Litman, M. Peng, Z. Jin et al., “BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ,” Cancer Cell, vol. 8, no. 3, pp. 255–265, 2005. View at Publisher · View at Google Scholar · View at Scopus
  19. S. Reid, D. Schindler, H. Hanenberg et al., “Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer,” Nature Genetics, vol. 39, no. 2, pp. 162–164, 2007. View at Publisher · View at Google Scholar · View at Scopus
  20. B. Xia, J. C. Dorsman, N. Ameziane et al., “Fanconi anemia is associated with a defect in the BRCA2 partner PALB2,” Nature Genetics, vol. 39, no. 2, pp. 159–161, 2007. View at Publisher · View at Google Scholar · View at Scopus
  21. Y. Kim, F. P. Lach, R. Desetty, H. Hanenberg, A. D. Auerbach, and A. Smogorzewska, “Mutations of the SLX4 gene in Fanconi anemia,” Nature Genetics, vol. 43, no. 2, pp. 142–146, 2011. View at Publisher · View at Google Scholar · View at Scopus
  22. C. Stoepker, K. Hain, B. Schuster et al., “SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype,” Nature Genetics, vol. 43, no. 2, pp. 138–141, 2011. View at Publisher · View at Google Scholar · View at Scopus
  23. A. Meindl, H. Hellebrand, C. Wiek et al., “Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene,” Nature Genetics, vol. 42, no. 5, pp. 410–414, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. F. Vaz, H. Hanenberg, B. Schuster et al., “Mutation of the RAD51C gene in a Fanconi anemia-like disorder,” Nature Genetics, vol. 42, no. 5, pp. 406–409, 2010. View at Publisher · View at Google Scholar · View at Scopus
  25. I. Garcia-Higuera, Y. Kuang, D. Näf, J. Wasik, and A. D. D'Andrea, “Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex,” Molecular and Cellular Biology, vol. 19, no. 7, pp. 4866–4873, 1999. View at Google Scholar · View at Scopus
  26. I. Garcia-Higuera, Y. Kuang, J. Denham, and A. D. D'Andrea, “The Fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the Fanconi anemia complex,” Blood, vol. 96, no. 9, pp. 3224–3230, 2000. View at Google Scholar · View at Scopus
  27. J. P. de Winter, L. van der Weel, J. De Groot et al., “The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG,” Human Molecular Genetics, vol. 9, no. 18, pp. 2665–2674, 2000. View at Google Scholar · View at Scopus
  28. A. L. Medhurst, P. A. J. Huber, Q. Waisfisz, J. P. de Winter, and C. G. Mathew, “Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway,” Human Molecular Genetics, vol. 10, no. 4, pp. 423–429, 2001. View at Google Scholar · View at Scopus
  29. C. Ling, M. Ishiai, A. M. Ali et al., “FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway,” The EMBO Journal, vol. 26, no. 8, pp. 2104–2114, 2007. View at Publisher · View at Google Scholar · View at Scopus
  30. A. Ciccia, C. Ling, R. Coulthard et al., “Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM,” Molecular Cell, vol. 25, no. 3, pp. 331–343, 2007. View at Publisher · View at Google Scholar · View at Scopus
  31. H. Kim et al., “Regulation of Rev1 by the Fanconi anemia core complex,” Nature Structural and Molecular Biology, vol. 19, no. 2, pp. 164–170, 2012. View at Publisher · View at Google Scholar
  32. A. M. Ali et al., “FAAP20: a novel ubiquitin-binding FA nuclear core complex protein required for functional integrity of the FA-BRCA DNA repair pathway,” Blood, vol. 119, no. 14, pp. 3285–3294, 2012. View at Google Scholar
  33. J. W. C. Leung, Y. Wang, K. W. Fong, M. S. Y. Huen, L. Li, and J. Chen, “Fanconi anemia (FA) binding protein FAAP20 stabilizes FA complementation group A (FANCA) and participates in interstrand cross-link repair,” Proceedings of the National Academy of Sciences, vol. 109, no. 12, pp. 4491–4496, 2012. View at Publisher · View at Google Scholar
  34. T. R. Singh, D. Saro, A. M. Ali et al., “MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM,” Molecular Cell, vol. 37, no. 6, pp. 879–886, 2010. View at Publisher · View at Google Scholar · View at Scopus
  35. Z. Yan, M. Delannoy, C. Ling et al., “A histone-fold complex and FANCM forma conserved DNA-remodeling complex to maintain genome stability,” Molecular Cell, vol. 37, no. 6, pp. 865–878, 2010. View at Publisher · View at Google Scholar · View at Scopus
  36. G. L. Moldovan and A. D. D'Andrea, “How the Fanconi anemia pathway guards the genome,” Annual Review of Genetics, vol. 43, no. 1, pp. 223–249, 2009. View at Publisher · View at Google Scholar · View at Scopus
  37. E. S. Zimmerman, B. A. Schulman, and N. Zheng, “Structural assembly of cullin-RING ubiquitin ligase complexes,” Current Opinion in Structural Biology, vol. 20, no. 6, pp. 714–721, 2010. View at Publisher · View at Google Scholar · View at Scopus
  38. A. Schreiber, F. Stengel, Z. Zhang et al., “Structural basis for the subunit assembly of the anaphase-promoting complex,” Nature, vol. 470, no. 7333, pp. 227–232, 2011. View at Publisher · View at Google Scholar · View at Scopus
  39. B. A. Buschhorn, G. Petzold, M. Galova et al., “Substrate binding on the APC/C occurs between the coactivator Cdh1 and the processivity factor Doc1,” Nature Structural and Molecular Biology, vol. 18, no. 1, pp. 6–13, 2011. View at Publisher · View at Google Scholar · View at Scopus
  40. P. C. A. da Fonseca, E. H. Kong, Z. Zhang et al., “Structures of APC/CCdh1 with substrates identify Cdh1 and Apc10 as the D-box co-receptor,” Nature, vol. 470, no. 7333, pp. 274–278, 2011. View at Publisher · View at Google Scholar · View at Scopus
  41. A. F. Alpi, P. E. Pace, M. M. Babu, and K. J. Patel, “Mechanistic insight into site-restricted monoubiquitination of FANCD2 by Ube2t, FANCL, and FANCI,” Molecular Cell, vol. 32, no. 6, pp. 767–777, 2008. View at Publisher · View at Google Scholar · View at Scopus
  42. A. R. Cole, L. P. C. Lewis, and H. Walden, “The structure of the catalytic subunit FANCL of the Fanconi anemia core complex,” Nature Structural and Molecular Biology, vol. 17, no. 3, pp. 294–298, 2010. View at Publisher · View at Google Scholar · View at Scopus
  43. Y. J. Machida, Y. Machida, Y. Chen et al., “UBE2T is the E2 in the Fanconi anemia pathway and undergoes negative autoregulation,” Molecular Cell, vol. 23, no. 4, pp. 589–596, 2006. View at Publisher · View at Google Scholar · View at Scopus
  44. C. Hodson, A. R. Cole, L. P. C. Lewis, J. A. Miles, A. P. Trew, and H. Walden, “Structural analysis of human FANCL, the E3 ligase in the Fanconi anemia pathway,” The Journal of Biological Chemistry, vol. 286, no. 37, pp. 32628–32637, 2011. View at Google Scholar
  45. P. Pace, M. Johnson, W. M. Tan et al., “FANCE: the link between Fanconi anaemia complex assembly and activity,” The EMBO Journal, vol. 21, no. 13, pp. 3414–3423, 2002. View at Publisher · View at Google Scholar · View at Scopus
  46. S. M. Gordon and M. Buchwald, “Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems,” Blood, vol. 102, no. 1, pp. 136–141, 2003. View at Publisher · View at Google Scholar · View at Scopus
  47. F. Léveillé, M. Ferrer, A. L. Medhurst et al., “The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCC,” DNA Repair, vol. 5, no. 5, pp. 556–565, 2006. View at Publisher · View at Google Scholar · View at Scopus
  48. R. K. Nookala, S. Hussain, and L. Pellegrini, “Insights into Fanconi anaemia from the structure of human FANCE,” Nucleic Acids Research, vol. 35, no. 5, pp. 1638–1648, 2007. View at Publisher · View at Google Scholar · View at Scopus
  49. S. Seki, M. Ohzeki, A. Uchida et al., “A requirement of FancL and FancD2 monoubiquitination in DNA repair,” Genes to Cells, vol. 12, no. 3, pp. 299–310, 2007. View at Publisher · View at Google Scholar · View at Scopus
  50. F. A. E. Kruyt, F. Abou-Zahr, H. Mok, and H. Youssoufian, “Resistance to mitomycin C requires direct interaction between the Fanconi anemia proteins FANCA and FANCG in the nucleus through an arginine- rich domain,” The Journal of Biological Chemistry, vol. 274, no. 48, pp. 34212–34218, 1999. View at Publisher · View at Google Scholar · View at Scopus
  51. Q. Waisfisz, J. P. de Winter, F. A. E. Kruyt et al., “A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 18, pp. 10320–10325, 1999. View at Publisher · View at Google Scholar · View at Scopus
  52. P. A. J. Huber, A. L. Medhurst, H. Youssoufian, and C. G. Mathew, “Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis,” Biochemical and Biophysical Research Communications, vol. 268, no. 1, pp. 73–77, 2000. View at Publisher · View at Google Scholar · View at Scopus
  53. T. Reuter, S. Herterich, O. Bernhard, H. Hoehn, and H. J. Gross, “Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system,” Blood, vol. 95, no. 2, pp. 719–720, 2000. View at Google Scholar · View at Scopus
  54. E. Blom, H. J. van de Vrugt, Y. De Vries, J. P. de Winter, F. Arwert, and H. Joenje, “Multiple TPR motifs characterize the Fanconi anemia FANCG protein,” DNA Repair, vol. 3, no. 1, pp. 77–84, 2004. View at Publisher · View at Google Scholar · View at Scopus
  55. S. Hussain, J. B. Wilson, E. Blom et al., “Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2,” DNA Repair, vol. 5, no. 5, pp. 629–640, 2006. View at Publisher · View at Google Scholar · View at Scopus
  56. J. B. Wilson, E. Blom, R. Cunningham, Y. Xiao, G. M. Kupfer, and N. J. Jones, “Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance,” Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, vol. 689, no. 1-2, pp. 12–20, 2010. View at Publisher · View at Google Scholar · View at Scopus
  57. D. Adachi, T. Oda, H. Yagasaki et al., “Heterogenous activation of the Fanconi anemia pathway by patient-derived FANCA mutants,” Human Molecular Genetics, vol. 11, no. 25, pp. 3125–3134, 2002. View at Google Scholar · View at Scopus
  58. D. Näf, G. M. Kupfer, A. Suliman, K. Lambert, and A. D. D'Andrea, “Functional activity of the Fanconi anemia protein FAA requires FAC binding and nuclear localization,” Molecular and Cellular Biology, vol. 18, no. 10, pp. 5952–5960, 1998. View at Google Scholar · View at Scopus
  59. F. Léveillé, E. Blom, A. L. Medhurst et al., “The Fanconi anemia gene product FANCF is a flexible adaptor protein,” The Journal of Biological Chemistry, vol. 279, no. 38, pp. 39421–39430, 2004. View at Publisher · View at Google Scholar · View at Scopus
  60. P. Kowal, A. M. Gurtan, P. Stuckert, A. D. D'Andrea, and T. Ellenberger, “Structural determinants of human FANCF protein that function in the assembly of a DNA damage signaling complex,” The Journal of Biological Chemistry, vol. 282, no. 3, pp. 2047–2055, 2007. View at Publisher · View at Google Scholar · View at Scopus
  61. S. M. Gordon, N. Alon, and M. Buchwald, “FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway,” The Journal of Biological Chemistry, vol. 280, no. 43, pp. 36118–36125, 2005. View at Publisher · View at Google Scholar · View at Scopus
  62. T. Taniguchi and A. D. D'Andrea, “The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC,” Blood, vol. 100, no. 7, pp. 2457–2462, 2002. View at Publisher · View at Google Scholar · View at Scopus
  63. A. L. Medhurst, E. H. Laghmani, J. Steltenpool et al., “Evidence for subcomplexes in the Fanconi anemia pathway,” Blood, vol. 108, no. 6, pp. 2072–2080, 2006. View at Publisher · View at Google Scholar · View at Scopus
  64. A. Alpi, F. Langevin, G. Mosedale, Y. J. Machida, A. Dutta, and K. J. Patel, “UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination,” Molecular and Cellular Biology, vol. 27, no. 24, pp. 8421–8430, 2007. View at Publisher · View at Google Scholar · View at Scopus
  65. T. Taniguchi, I. Garcia-Higuera, P. R. Andreassen, R. C. Gregory, M. Grompe, and A. D. D'Andrea, “S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51,” Blood, vol. 100, no. 7, pp. 2414–2420, 2002. View at Publisher · View at Google Scholar · View at Scopus
  66. X. Wang, P. R. Andreassen, and A. D. D'Andrea, “Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin,” Molecular and Cellular Biology, vol. 24, no. 13, pp. 5850–5862, 2004. View at Publisher · View at Google Scholar · View at Scopus
  67. J. Wang, T. R. Sarkar, M. Zhou et al., “CCAAT/enhancer binding protein delta (C/EBPδ, CEBPD)-mediated nuclear import of FANCD2 by IPO4 augments cellular response to DNA damage,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 37, pp. 16131–16136, 2010. View at Publisher · View at Google Scholar · View at Scopus
  68. P. S. Rudland, A. M. Platt-Higgins, L. M. Davies et al., “Significance of the Fanconi anemia FANCD2 protein in sporadic and metastatic human breast cancer,” American Journal of Pathology, vol. 176, no. 6, pp. 2935–2947, 2010. View at Publisher · View at Google Scholar · View at Scopus
  69. D. J. Ma, S. J. Li, L. S. Wang, J. Dai, S. L. Zhao, and R. Zeng, “Temporal and spatial profiling of nuclei-associated proteins upon TNF-α/NF-κB signaling,” Cell Research, vol. 19, no. 5, pp. 651–664, 2009. View at Publisher · View at Google Scholar · View at Scopus
  70. A. Borriello, A. Locasciulli, A. M. Bianco et al., “A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia,” Leukemia, vol. 21, no. 1, pp. 72–78, 2007. View at Publisher · View at Google Scholar · View at Scopus
  71. T. Yamashita, D. L. Barber, Y. Zhu, N. Wu, and A. D. D'Andrea, “The Fanconi anemia polypeptide FACC is localized to the cytoplasm,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 14, pp. 6712–6716, 1994. View at Publisher · View at Google Scholar · View at Scopus
  72. A. R. Meetei, S. Sechi, M. Wallisch et al., “A multiprotein nuclear complex connects Fanconi anemia and bloom syndrome,” Molecular and Cellular Biology, vol. 23, no. 10, pp. 3417–3426, 2003. View at Publisher · View at Google Scholar · View at Scopus
  73. A. Thomashevski, A. A. High, M. Drozd et al., “The Fanconi anemia core complex forms four complexes of different sizes in different subcellular compartments,” The Journal of Biological Chemistry, vol. 279, no. 25, pp. 26201–26209, 2004. View at Publisher · View at Google Scholar · View at Scopus
  74. A. J. Deans and S. C. West, “FANCM connects the genome instability disorders bloom's syndrome and Fanconi anemia,” Molecular Cell, vol. 36, no. 6, pp. 943–953, 2009. View at Publisher · View at Google Scholar · View at Scopus
  75. G. Mosedale, W. Niedzwiedz, A. Alpi et al., “The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway,” Nature Structural and Molecular Biology, vol. 12, no. 9, pp. 763–771, 2005. View at Publisher · View at Google Scholar · View at Scopus
  76. Y. Xue, Y. Li, R. Guo, C. Ling, and W. Wang, “FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair,” Human Molecular Genetics, vol. 17, no. 11, pp. 1641–1652, 2008. View at Publisher · View at Google Scholar · View at Scopus
  77. J. M. Kim, Y. Kee, A. Gurtan, and A. D. D'Andrea, “Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24,” Blood, vol. 111, no. 10, pp. 5215–5222, 2008. View at Publisher · View at Google Scholar · View at Scopus
  78. H. Yang et al., “Saccharomyces cerevisiae MHF complex structurally resembles the histones (H3-H4)2 heterotetramer and functions as a heterotetramer,” Structure, vol. 20, no. 2, pp. 364–370, 2012. View at Google Scholar
  79. S. J. Collis, A. Ciccia, A. J. Deans et al., “FANCM and FAAP24 function in ATR-mediated checkpoint signaling independently of the Fanconi anemia core complex,” Molecular Cell, vol. 32, no. 3, pp. 313–324, 2008. View at Publisher · View at Google Scholar · View at Scopus