PUBLICATIONS

1. Rojas, V., Salinas, F., Romero, A., Larrondo, L.F., Canessa, P., 2022. Interactions between Core Elements of the Botrytis cinerea Circadian Clock Are Modulated by Light and Different Protein Domains. J Fungi  8. https://doi.org/10.3390/jof8050486
2. Figueroa, D., Rojas, V., Romero, A., Larrondo, L.F., Salinas, F., 2021. The rise and shine of yeast optogenetics. Yeast 38, 131–146. https://doi.org/10.1002/yea.3529
3. Muñoz-Guzmán, F., Caballero, V., Larrondo, L.F., 2021. A Global Search for novel Transcription Factors impacting the Neurospora crassa Circadian Clock. G3  11. https://doi.org/10.1093/g3journal/jkab100
4. Olivares-Yañez, C., Sánchez, E., Pérez-Lara, G., Seguel, A., Camejo, P.Y., Larrondo, L.F., Vidal, E.A., Canessa, P., 2021. A comprehensive transcription factor and DNA-binding motif resource for the construction of gene regulatory networks in Botrytis cinerea and Trichoderma  atroviride. Comput Struct Biotechnol J 19, 6212–6228. https://doi.org/10.1016/j.csbj.2021.11.012
5. Romero, A., Rojas, V., Delgado, V., Salinas, F., Larrondo, L.F., 2021. Modular and Molecular Optimization of a LOV (Light-Oxygen-Voltage)-Based Optogenetic Switch in Yeast. Int J Mol Sci 22. https://doi.org/10.3390/ijms22168538
6. Díaz, R.D., Larrondo, L.F., 2020. A circadian clock in Neurospora crassa functions during plant cell wall deconstruction. Fungal Biol 124, 501–508. https://doi.org/10.1016/j.funbio.2020.03.003
7. Nespolo, R.F., Villarroel, C.A., Oporto, C.I., Tapia, S.M., Vega-Macaya, F., Urbina, K., De Chiara, M., Mozzachiodi, S., Mikhalev, E., Thompson, D., Larrondo, L.F., Saenz-Agudelo, P., Liti, G., Cubillos, F.A., 2020. An Out-of-Patagonia migration explains the worldwide diversity and distribution of Saccharomyces eubayanus lineages. PLoS Genet 16, e1008777. https://doi.org/10.1371/journal.pgen.1008777
8. Horta, M.A.C., Thieme, N., Gao, Y., Burnum-Johnson, K.E., Nicora, C.D., Gritsenko, M.A., Lipton, M.S., Mohanraj, K., de Assis, L.J., Lin, L., Tian, C., Braus, G.H., Borkovich, K.A., Schmoll, M., Larrondo, L.F., Samal, A., Goldman, G.H., Benz, J.P., 2019. Broad Substrate-Specific Phosphorylation Events Are Associated With the Initial Stage of Plant Cell Wall Recognition in Neurospora crassa. Front Microbiol 10, 2317. https://doi.org/10.3389/fmicb.2019.02317
9. Kessi-Pérez, E.I., Salinas, F., González, A., Su, Y., Guillamón, J.M., Hall, M.N., Larrondo, L.F., Martínez, C., 2019a. KAE1 Allelic Variants Affect TORC1 Activation and Fermentation Kinetics in Saccharomyces cerevisiae. Front Microbiol 10, 1686. https://doi.org/10.3389/fmicb.2019.01686
10. Kessi-Pérez, E.I., Salinas, F., Molinet, J., González, A., Muñiz, S., Guillamón, J.M., Hall, M.N., Larrondo, L.F., Martínez, C., 2019b. Indirect monitoring of TORC1 signalling pathway reveals molecular diversity among different yeast strains. Yeast 36, 65–74.https://doi.org/10.1002/yea.3351
11. Larrondo, L.F., Canessa, P., 2019. The Clock Keeps on Ticking: Emerging Roles for Circadian Regulation in the Control of Fungal Physiology and Pathogenesis. Curr Top Microbiol Immunol 422, 121–156. https://doi.org/10.1007/82_2018_143
12. Boni, A.C., Ambrósio, D.L., Cupertino, F.B., Montenegro-Montero, A., Virgilio, S., Freitas, F.Z., Corrocher, F.A., Gonçalves, R.D., Yang, A., Weirauch, M.T., Hughes, T.R., Larrondo, L.F., Bertolini, M.C., 2018. Neurospora crassa developmental control mediated by the FLB-3 transcription factor. Fungal Biol 122, 570–582. https://doi.org/10.1016/j.funbio.2018.01.004
13. Rojas-Aedo, J.F., Gil-Durán, C., Goity, A., Vaca, I., Levicán, G., Larrondo, L.F., Chávez, R., 2018. The developmental regulator Pcz1 affects the production of secondary metabolites in the filamentous fungus Penicillium roqueforti. Microbiol Res 212–213, 67–74. https://doi.org/10.1016/j.micres.2018.05.005
14. Salinas, F., Rojas, V., Delgado, V., López, J., Agosin, E., Larrondo, L.F., 2018. Fungal Light-Oxygen-Voltage Domains for Optogenetic Control of Gene Expression and Flocculation in Yeast. mBio 9. https://doi.org/10.1128/mBio.00626-18
15. Tapia, S.M., Cuevas, M., Abarca, V., Delgado, V., Rojas, V., García, V., Brice, C., Martínez, C., Salinas, F., Larrondo, L.F., Cubillos, F.A., 2018. GPD1 and ADH3 Natural Variants Underlie Glycerol Yield Differences in Wine Fermentation. Front Microbiol 9, 1460. https://doi.org/10.3389/fmicb.2018.01460
16. Castillo, L., Plaza, V., Larrondo, L.F., Canessa, P., 2017. Recent Advances in the Study of the Plant Pathogenic Fungus Botrytis cinerea and its Interaction with the Environment. Curr Protein Pept Sci 18, 976–989. https://doi.org/10.2174/1389203717666160809160915
17. Franco, D.L., Canessa, P., Bellora, N., Risau-Gusman, S., Olivares-Yañez, C., Pérez-Lara, R., Libkind, D., Larrondo, L.F., Marpegan, L., 2017. Spontaneous circadian rhythms in a cold-adapted natural isolate of Aureobasidium pullulans. Sci Rep 7, 13837. https://doi.org/10.1038/s41598-017-14085-6
18. Gaskell, J., Kersten, P., Larrondo, L.F., Canessa, P., Martinez, D., Hibbett, D., Schmoll, M., Kubicek, C.P., Martinez, A.T., Yadav, J., Master, E., Magnuson, J.K., Yaver, D., Berka, R., Lail, K., Chen, C., LaButti, K., Nolan, M., Lipzen, A., Aerts, A., Riley, R., Barry, K., Henrissat, B., Blanchette, R., Grigoriev, I.V., Cullen, D., 2017. Draft genome sequence of a monokaryotic model brown-rot fungus Postia (Rhodonia) placenta SB12. Genom Data 14, 21–23. https://doi.org/10.1016/j.gdata.2017.08.003
19. Salinas, F., Rojas, V., Delgado, V., Agosin, E., Larrondo, L.F., 2017. Optogenetic switches for light-controlled gene expression in yeast. Appl Microbiol Biotechnol 101, 2629–2640. https://doi.org/10.1007/s00253-017-8178-8
20. Hevia, M.A., Canessa, P., Larrondo, L.F., 2016. Circadian clocks and the regulation of virulence in fungi: Getting up to speed. Semin Cell Dev Biol 57, 147–155. https://doi.org/10.1016/j.semcdb.2016.03.021
21. Kessi-Pérez, E.I., Araos, S., García, V., Salinas, F., Abarca, V., Larrondo, L.F., Martínez, C., Cubillos, F.A., 2016. RIM15 antagonistic pleiotropy is responsible for differences in fermentation and stress response kinetics in budding yeast. FEMS Yeast Res 16, fow021. https://doi.org/10.1093/femsyr/fow021
22. Montenegro-Montero, A., Larrondo, L.F., 2016. In the Driver’s Seat: The Case for Transcriptional Regulation and Coupling as Relevant Determinants of the Circadian Transcriptome and Proteome in Eukaryotes. J Biol Rhythms 31, 37–47. https://doi.org/10.1177/0748730415607321
23. Olivares-Yañez, C., Emerson, J., Kettenbach, A., Loros, J.J., Dunlap, J.C., Larrondo, L.F., 2016. Modulation of Circadian Gene Expression and Metabolic Compensation by the RCO-1 Corepressor of Neurospora crassa. Genetics 204, 163–176. https://doi.org/10.1534/genetics.116.191064
24. Salinas, F., de Boer, C.G., Abarca, V., García, V., Cuevas, M., Araos, S., Larrondo, L.F., Martínez, C., Cubillos, F.A., 2016. Natural variation in non-coding regions underlying phenotypic diversity in budding yeast. Sci Rep 6, 21849. https://doi.org/10.1038/srep21849
25. Feeney, K.A., Hansen, L.L., Putker, M., Olivares-Yañez, C., Day, J., Eades, L.J., Larrondo, L.F., Hoyle, N.P., O’Neill, J.S., van Ooijen, G., 2016. Daily magnesium fluxes regulate cellular timekeeping and energy balance. Nature 532, 375–379. https://doi.org/10.1038/nature17407
26. Hevia, M.A., Canessa, P., Müller-Esparza, H., Larrondo, L.F., 2015. A circadian oscillator in the fungus Botrytis cinerea regulates virulence when infecting Arabidopsis thaliana. Proc Natl Acad Sci U S A 112, 8744–8749. https://doi.org/10.1073/pnas.1508432112
27. Larrondo, L.F., Olivares-Yañez, C., Baker, C.L., Loros, J.J., Dunlap, J.C., 2015. Circadian rhythms. Decoupling circadian clock protein turnover from circadian period determination. Science 347, 1257277. https://doi.org/10.1126/science.1257277
28. Montenegro-Montero, A., Canessa, P., Larrondo, L.F., 2015a. Around the Fungal Clock: Recent Advances in the Molecular Study of Circadian Clocks in Neurospora and Other Fungi. Adv Genet 92, 107–184. https://doi.org/10.1016/bs.adgen.2015.09.003
29. Montenegro-Montero, A., Goity, A., Larrondo, L.F., 2015b. The bZIP Transcription Factor HAC-1 Is Involved in the Unfolded Protein Response and Is Necessary for Growth on Cellulose in Neurospora crassa. PLoS One 10, e0131415. https://doi.org/10.1371/journal.pone.0131415
30. Plaza, V., Lagües, Y., Carvajal, M., Pérez-García, L.A., Mora-Montes, H.M., Canessa, P., Larrondo, L.F., Castillo, L., 2015. bcpmr1 encodes a P-type Ca(2+)/Mn(2+)-ATPase mediating cell-wall integrity and virulence in the phytopathogen Botrytis cinerea. Fungal Genet Biol 76, 36–46. https://doi.org/10.1016/j.fgb.2015.01.012
31. Gooch, V.D., Johnson, A.E., Bourne, B.J., Nix, B.T., Maas, J.A., Fox, J.A., Loros, J.J., Larrondo, L.F., Dunlap, J.C., 2014a. A kinetic study of the effects of light on circadian rhythmicity of the frq promoter of Neurospora crassa. J Biol Rhythms 29, 38–48. https://doi.org/10.1177/0748730413517981
32. Gooch, V.D., Johnson, A.E., Larrondo, L.F., Loros, J.J., Dunlap, J.C., 2014b. Bright to dim oscillatory response of the Neurospora circadian oscillator. J Biol Rhythms 29, 49–59. https://doi.org/10.1177/0748730413517983
33. Hong, C.I., Zámborszky, J., Baek, M., Labiscsak, L., Ju, K., Lee, H., Larrondo, L.F., Goity, A., Chong, H.S., Belden, W.J., Csikász-Nagy, A., 2014. Circadian rhythms synchronize mitosis in Neurospora crassa. Proc Natl Acad Sci U S A 111, 1397–1402. https://doi.org/10.1073/pnas.1319399111
34. Hori, C., Ishida, T., Igarashi, K., Samejima, M., Suzuki, H., Master, E., Ferreira, P., Ruiz-Dueñas, F.J., Held, B., Canessa, P., Larrondo, L.F., Schmoll, M., Druzhinina, I.S., Kubicek, C.P., Gaskell, J.A., Kersten, P., St John, F., Glasner, J., Sabat, G., Splinter BonDurant, S., Syed, K., Yadav, J., Mgbeahuruike, A.C., Kovalchuk, A., Asiegbu, F.O., Lackner, G., Hoffmeister, D., Rencoret, J., Gutiérrez, A., Sun, H., Lindquist, E., Barry, K., Riley, R., Grigoriev, I.V., Henrissat, B., Kües, U., Berka, R.M., Martínez, A.T., Covert, S.F., Blanchette, R.A., Cullen, D., 2014. Analysis of the Phlebiopsis gigantea genome, transcriptome and secretome provides insight into its pioneer colonization strategies of wood. PLoS Genet 10, e1004759. https://doi.org/10.1371/journal.pgen.1004759
35. Weirauch, M.T., Yang, A., Albu, M., Cote, A.G., Montenegro-Montero, A., Drewe, P., Najafabadi, H.S., Lambert, S.A., Mann, I., Cook, K., Zheng, H., Goity, A., van Bakel, H., Lozano, J.-C., Galli, M., Lewsey, M.G., Huang, E., Mukherjee, T., Chen, X., Reece-Hoyes, J.S., Govindarajan, S., Shaulsky, G., Walhout, A.J.M., Bouget, F.-Y., Ratsch, G., Larrondo, L.F., Ecker, J.R., Hughes, T.R., 2014. Determination and inference of eukaryotic transcription factor sequence specificity. Cell 158, 1431–1443. https://doi.org/10.1016/j.cell.2014.08.009
36. Canessa, P., Larrondo, L.F., 2013. Environmental responses and the control of iron homeostasis in fungal systems. Appl Microbiol Biotechnol 97, 939–955. https://doi.org/10.1007/s00253-012-4615-x
37. Canessa, P., Schumacher, J., Hevia, M.A., Tudzynski, P., Larrondo, L.F., 2013. Assessing the effects of light on differentiation and virulence of the plant pathogen Botrytis cinerea: characterization of the White Collar Complex. PLoS One 8, e84223. https://doi.org/10.1371/journal.pone.0084223
38. Hurley, J.M., Larrondo, L.F., Loros, J.J., Dunlap, J.C., 2013. Conserved RNA helicase FRH acts nonenzymatically to support the intrinsically disordered neurospora clock protein FRQ. Mol Cell 52, 832–843. https://doi.org/10.1016/j.molcel.2013.11.005
39. Canessa, P., Muñoz-Guzmán, F., Vicuña, R., Larrondo, L.F., 2012. Characterization of PIR1, a GATA family transcription factor involved in iron responses in the white-rot fungus Phanerochaete chrysosporium. Fungal Genet Biol 49, 626–634. https://doi.org/10.1016/j.fgb.2012.05.013
40. Fernandez-Fueyo, E., Ruiz-Dueñas, F.J., Ferreira, P., Floudas, D., Hibbett, D.S., Canessa, P., Larrondo, L.F., James, T.Y., Seelenfreund, D., Lobos, S., Polanco, R., Tello, M., Honda, Y., Watanabe, Takahito, Watanabe, Takashi, Ryu, J.S., Kubicek, C.P., Schmoll, M., Gaskell, J., Hammel, K.E., St John, F.J., Vanden Wymelenberg, A., Sabat, G., Splinter BonDurant, S., Syed, K., Yadav, J.S., Doddapaneni, H., Subramanian, V., Lavín, J.L., Oguiza, J.A., Perez, G., Pisabarro, A.G., Ramirez, L., Santoyo, F., Master, E., Coutinho, P.M., Henrissat, B., Lombard, V., Magnuson, J.K., Kües, U., Hori, C., Igarashi, K., Samejima, M., Held, B.W., Barry, K.W., LaButti, K.M., Lapidus, A., Lindquist, E.A., Lucas, S.M., Riley, R., Salamov, A.A., Hoffmeister, D., Schwenk, D., Hadar, Y., Yarden, O., de Vries, R.P., Wiebenga, A., Stenlid, J., Eastwood, D., Grigoriev, I.V., Berka, R.M., Blanchette, R.A., Kersten, P., Martinez, A.T., Vicuna, R., Cullen, D., 2012. Comparative genomics of Ceriporiopsis subvermispora and Phanerochaete chrysosporium provide insight into selective ligninolysis. Proc Natl Acad Sci U S A 109, 5458–5463. https://doi.org/10.1073/pnas.1119912109
41. Floudas, D., Binder, M., Riley, R., Barry, K., Blanchette, R.A., Henrissat, B., Martínez, A.T., Otillar, R., Spatafora, J.W., Yadav, J.S., Aerts, A., Benoit, I., Boyd, A., Carlson, A., Copeland, A., Coutinho, P.M., de Vries, R.P., Ferreira, P., Findley, K., Foster, B., Gaskell, J., Glotzer, D., Górecki, P., Heitman, J., Hesse, C., Hori, C., Igarashi, K., Jurgens, J.A., Kallen, N., Kersten, P., Kohler, A., Kües, U., Kumar, T.K.A., Kuo, A., LaButti, K., Larrondo, L.F., Lindquist, E., Ling, A., Lombard, V., Lucas, S., Lundell, T., Martin, R., McLaughlin, D.J., Morgenstern, I., Morin, E., Murat, C., Nagy, L.G., Nolan, M., Ohm, R.A., Patyshakuliyeva, A., Rokas, A., Ruiz-Dueñas, F.J., Sabat, G., Salamov, A., Samejima, M., Schmutz, J., Slot, J.C., St John, F., Stenlid, J., Sun, H., Sun, S., Syed, K., Tsang, A., Wiebenga, A., Young, D., Pisabarro, A., Eastwood, D.C., Martin, F., Cullen, D., Grigoriev, I.V., Hibbett, D.S., 2012. The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes. Science 336, 1715–1719. https://doi.org/10.1126/science.1221748
42. Larrondo, L.F., Loros, J.J., Dunlap, J.C., 2012. High-resolution spatiotemporal analysis of gene expression in real time: in vivo analysis of circadian rhythms in Neurospora crassa using a FREQUENCY-luciferase  translational reporter. https://doi.org/10.1016/j.fgb.2012.06.001
43. Rodríguez-Rincón, F., Suarez, A., Lucas, M., Larrondo, L.F., de la Rubia, T., Polaina, J., Martínez, J., 2010. Molecular and structural modeling of the Phanerochaete flavido-alba extracellular laccase reveals its ferroxidase structure. Arch Microbiol 192, 883–892.https://doi.org/10.1007/s00203-010-0616-2
44. Larrondo, L.F., Colot, H.V., Baker, C.L., Loros, J.J., Dunlap, J.C., 2009. Fungal functional genomics: tunable knockout-knock-in expression and tagging strategies. Eukaryot Cell 8, 800–804. https://doi.org/10.1128/EC.00072-09
45. Martinez, D., Challacombe, J., Morgenstern, I., Hibbett, D., Schmoll, M., Kubicek, C.P., Ferreira, P., Ruiz-Duenas, F.J., Martinez, A.T., Kersten, P., Hammel, K.E., Vanden Wymelenberg, A., Gaskell, J., Lindquist, E., Sabat, G., Bondurant, S.S., Larrondo, L.F., Canessa, P., Vicuna, R., Yadav, J., Doddapaneni, H., Subramanian, V., Pisabarro, A.G., Lavín, J.L., Oguiza, J.A., Master, E., Henrissat, B., Coutinho, P.M., Harris, P., Magnuson, J.K., Baker, S.E., Bruno, K., Kenealy, W., Hoegger, P.J., Kües, U., Ramaiya, P., Lucas, S., Salamov, A., Shapiro, H., Tu, H., Chee, C.L., Misra, M., Xie, G., Teter, S., Yaver, D., James, T., Mokrejs, M., Pospisek, M., Grigoriev, I.V., Brettin, T., Rokhsar, D., Berka, R., Cullen, D., 2009. Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion. Proc Natl Acad Sci U S A 106, 1954–1959. https://doi.org/10.1073/pnas.0809575106
46. Colombres, M., Garate, J.A., Lagos, C.F., Araya-Secchi, R., Norambuena, P., Quiroz, S., Larrondo, L., Pérez-Acle, T., Eyzaguirre, J., 2008. An eleven amino acid residue deletion expands the substrate specificity of acetyl xylan esterase II (AXE II) from Penicillium purpurogenum. J Comput Aided Mol Des 22, 19–28. https://doi.org/10.1007/s10822-007-9149-4
47. Díaz, J., Chávez, R., Larrondo, L.F., Eyzaguirre, J., Bull, P., 2008. Functional analysis of the endoxylanase B (xynB) promoter from Penicillium purpurogenum. Curr Genet 54, 133–141. https://doi.org/10.1007/s00294-008-0205-y
48. Gooch, V.D., Mehra, A., Larrondo, L.F., Fox, J., Touroutoutoudis, M., Loros, J.J., Dunlap, J.C., 2008. Fully codon-optimized luciferase uncovers novel temperature characteristics of the Neurospora clock. Eukaryot Cell 7, 28–37. https://doi.org/10.1128/EC.00257-07
49. Martinez, D., Berka, R.M., Henrissat, B., Saloheimo, M., Arvas, M., Baker, S.E., Chapman, J., Chertkov, O., Coutinho, P.M., Cullen, D., Danchin, E.G.J., Grigoriev, I.V., Harris, P., Jackson, M., Kubicek, C.P., Han, C.S., Ho, I., Larrondo, L.F., de Leon, A.L., Magnuson, J.K., Merino, S., Misra, M., Nelson, B., Putnam, N., Robbertse, B., Salamov, A.A., Schmoll, M., Terry, A., Thayer, N., Westerholm-Parvinen, A., Schoch, C.L., Yao, J., Barabote, R., Nelson, M.A., Detter, C., Bruce, D., Kuske, C.R., Xie, G., Richardson, P., Rokhsar, D.S., Lucas, S.M., Rubin, E.M., Dunn-Coleman, N., Ward, M., Brettin, T.S., 2008. Genome sequencing and analysis of the biomass-degrading fungus Trichoderma reesei (syn. Hypocrea jecorina). Nat Biotechnol 26, 553–560. https://doi.org/10.1038/nbt1403
50. Belden, W.J., Larrondo, L.F., Froehlich, A.C., Shi, M., Chen, C.-H., Loros, J.J., Dunlap, J.C., 2007. The band mutation in Neurospora crassa is a dominant allele of ras-1 implicating RAS signaling in circadian output. Genes Dev 21, 1494–1505. https://doi.org/10.1101/gad.1551707
51. Dunlap, J.C., Loros, J.J., Colot, H.V., Mehra, A., Belden, W.J., Shi, M., Hong, C.I., Larrondo, L.F., Baker, C.L., Chen, C.-H., Schwerdtfeger, C., Collopy, P.D., Gamsby, J.J., Lambreghts, R., 2007. A circadian clock in Neurospora: how genes and proteins cooperate to produce a sustained, entrainable, and compensated biological oscillator with a period of  about a day. Cold Spring Harb Symp Quant Biol 72, 57–68. https://doi.org/10.1101/sqb.2007.72.072
52. Larrondo, L.F., Canessa, P., Melo, F., Polanco, R., Vicuña, R., 2007a. Cloning and characterization of the genes encoding the high-affinity iron-uptake protein complex Fet3/Ftr1 in the basidiomycete Phanerochaete chrysosporium. Microbiology (Reading) 153, 1772–1780. https://doi.org/10.1099/mic.0.2006/003442-0
53. Larrondo, L.F., Canessa, P., Vicuña, R., Stewart, P., Vanden Wymelenberg, A., Cullen, D., 2007b. Structure and transcriptional impact of divergent repetitive elements inserted within Phanerochaete chrysosporium strain RP-78 genes. Mol Genet Genomics 277, 43–55. https://doi.org/10.1007/s00438-006-0167-z
54. Loros, J.J., Dunlap, J.C., Larrondo, L.F., Shi, M., Belden, W.J., Gooch, V.D., Chen, C.-H., Baker, C.L., Mehra, A., Colot, H.V., Schwerdtfeger, C., Lambreghts, R., Collopy, P.D., Gamsby, J.J., Hong, C.I., 2007. Circadian output, input, and intracellular oscillators: insights into the circadian systems of single cells. Cold Spring Harb Symp Quant Biol 72, 201–214. https://doi.org/10.1101/sqb.2007.72.067
55. Shi, M., Larrondo, L.F., Loros, J.J., Dunlap, J.C., 2007. A developmental cycle masks output from the circadian oscillator under conditions of choline deficiency in Neurospora. Proc Natl Acad Sci U S A 104, 20102–20107. https://doi.org/10.1073/pnas.0706631104
56. Polanco, R., Canessa, P., Rivas, A., Larrondo, L.F., Lobos, S., Vicuña, R., 2006. Cloning and functional characterization of the gene encoding the transcription factor Ace1 in the basidiomycete Phanerochaete chrysosporium. Biol Res 39, 641–648. https://doi.org/10.4067/s0716-97602006000500007
57. Varela-Nallar, L., Toledo, E.M., Larrondo, L.F., Cabral, A.L.B., Martins, V.R., Inestrosa, N.C., 2006. Induction of cellular prion protein gene expression by copper in neurons. Am J Physiol Cell Physiol 290, C271-281. https://doi.org/10.1152/ajpcell.00160.2005
58. Larrondo, L., Gonzalez, A., Perez Acle, T., Cullen, D., Vicuña, R., 2005. The nop gene from Phanerochaete chrysosporium encodes a peroxidase with novel structural features. Biophys Chem 116, 167–173. https://doi.org/10.1016/j.bpc.2005.03.006
59. Macarena, S., Fernando, L.L., Mónica, V., Rafael, V., Bernardo, G., 2005. Incomplete processing of peroxidase transcripts in the lignin degrading fungus Phanerochaete chrysosporium. FEMS Microbiol Lett 242, 37–44. https://doi.org/10.1016/j.femsle.2004.10.037
60. Larrondo, L.F., González, B., Cullen, D., Vicuña, R., 2004. Characterization of a multicopper oxidase gene cluster in Phanerochaete chrysosporium and evidence of altered splicing of the mco transcripts. Microbiology (Reading) 150, 2775–2783. https://doi.org/10.1099/mic.0.27072-0
61. Martinez, D., Larrondo, L.F., Putnam, N., Gelpke, M.D.S., Huang, K., Chapman, J., Helfenbein, K.G., Ramaiya, P., Detter, J.C., Larimer, F., Coutinho, P.M., Henrissat, B., Berka, R., Cullen, D., Rokhsar, D., 2004. Genome sequence of the lignocellulose degrading fungus Phanerochaete chrysosporium strain RP78. Nat Biotechnol 22, 695–700. https://doi.org/10.1038/nbt967
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