دورية أكاديمية

The chromatin landscape of healthy and injured cell types in the human kidney

التفاصيل البيبلوغرافية
العنوان: The chromatin landscape of healthy and injured cell types in the human kidney
المؤلفون: Gisch, D.L., Brennan, M., Lake, B.B., Basta, J., Keller, M.S., Melo, Ferreira, R., Akilesh, S., Ghag, R., Lu, C., Cheng, Y.-H., Collins, K.S., Parikh, S.V., Rovin, B.H., Robbins, L., Stout, L., Conklin, K.Y., Diep, D., Zhang, B., Knoten, A., Barwinska, D., Asghari, M., Sabo, A.R., Ferkowicz, M.J., Sutton, T.A., Kelly, K.J., De, Boer, I.H., Rosas, S.E., Kiryluk, K., Hodgin, J.B., Alakwaa, F., Winfree, S., Jefferson, N., Türkmen, A., Gaut, J.P., Gehlenborg, N., Phillips, C.L., El-Achkar, T.M., Dagher, P.C., Hato, T., Zhang, K., Himmelfarb, J., Kretzler, M., Mollah, S., Lake, B., Morales, A., Stillman, I., Lecker, S., Bogen, S., Verma, A., Yu, G., Schmidt, I., Henderson, J., Beck, L., Yadati, P., Waikar, S., Amodu, A.A., Maikhor, S., Ilori, T., Colona, M.R., Weins, A., McMahon, G., Hacohen, N., Greka, A., Marshall, J.L., Hoover, P.J., Viswanathan, V.S., Crawford, D., Aulisio, M., Bush, W., Chen, Y., Madabhushi, A., O’Malley, C., Gadegbeku, C., Sendrey, D., Poggio, E., O’Toole, J., Sedor, J., Taliercio, J., Bush, L., Herlitz, L., Palmer, E., Nguyen, J., Spates-Harden, K., Cooperman, L., Jolly, S., Vinovskis, C., Bomback, A., Barasch, J., Appelbaum, P., D’Agati, V., Berrouet, C., Mehl, K., Sabatello, M., Shang, N., Balderes, O., Canetta, P.A., Kudose, S., de, Pinho, Gonçalves, J., Migas, L., Van, de, Plas, R., Lardenoije, R., Barisoni, L., Rennke, H., Verdoes, A., Sabo, A., Williams, J., Kelly, K., Dunn, K., Eadon, M., Ferkowicz, M., Dagher, P., Bledsoe, S., Wofford, S., (El-Achkar), T.A., Sutton, T., Bowen, W., Slade, A., Record, E., Cheng, Y., Jain, Y., Herr, B., Quardokus, E., Wang, A., Villalobos, C.P.C., Parikh, C., Atta, M., Menez, S., Wen, Y., Xu, A., Bernard, L., Johansen, C., Chen, S., Rosas, S., Donohoe, I., Sun, J., Knight, R., Shpigel, A., Bebiak, J., Saul, J., Ardayfio, J., Koewler, R., Pinkeney, R., Campbell, T., Azeloglu, E., Nadkarni, G., He, J., Tokita, J., Campbell, K., Patel, M., Lefferts, S., Iyengar, S.R., Ward, S., Coca, S., He, C., Xiong, Y., Prasad, P., Rovin, B., Shapiro, J.P., Parikh, S., Madhavan, S.M., Lukowski, J., Velickovic, D., Pasa-Tolic, L., Oliver, G.H., Troyanskaya, O., Sealfon, R., Mao, W., Wong, A., Pollack, A., Goltsev, Y., Ginley, B., Lutnick, B., Nolan, G., Anjani, K., Mukatash, T., Laszik, Z.G., Campos, B., Thajudeen, B., Beyda, D., Bracamonte, E., Brosius, F., Woodhead, G., Mendoza, K., Marquez, N., Scott, R., Tsosie, R., Saunders, M., Rike, A., Woodle, E.S., Lee, P.J., Alloway, R.R., Shi, T., Hsieh, E., Kendrick, J., Thurman, J., Wrobel, J., Pyle, L., Bjornstad, P., Lucarelli, N., Sarder, P., Renteria, A., Ricardo, A., Srivastava, A., Redmond, D., Carmona-Powell, E., Bui, J., Lash, J., Fox, M., Meza, N., Gaba, R., Setty, S., Kelly, T., Lienczewski, C., Demeke, D., Otto, E., Ascani, H., Hodgin, J., Schaub, J., Hartman, J., Mariani, L., Bitzer, M., Rose, M., Bonevich, N., Conser, N., McCown, P., Dull, R., Menon, R., Reamy, R., Eddy, S., Balis, U., Blanc, V., Nair, V., He, Y.O., Wright, Z., Steck, B., Luo, J., Frey, R., Coleman, A., Henderson-Brown, D., Berge, J., Caramori, M.L., Adeyi, O., Nachman, P., Safadi, S., Flanagan, S., Ma, S., Klett, S., Wolf, S., Harindhanavudhi, T., Rao, V., Mottl, A., Froment, A., Zeitler, E., Bream, P., Kelley, S., Rosengart, M., Elder, M., Palevsky, P., Murugan, R., Hall, D.E., Bender, F., Winters, J., Kellum, J.A., Gilliam, M., Tublin, M., Tan, R., Zhang, G., Sharma, K., Venkatachalam, M., Hendricks, A., Kermani, A., Torrealba, J., Vazquez, M., Wang, N., Cai, Q., Miller, R.T., Hedayati, S., Hoofnagle, A., Wangperawong, A., Berglund, A., Dighe, A.L., Young, B., Larson, B., Berry, B., Alpers, C., Limonte, C., Stutzke, C., Roberts, G., de, Boer, I., Snyder, J., Phuong, J., Carson, J., Rezaei, K., Tuttle, K., Brown, K., Blank, K., Sarkisova, N., McClelland, R., Mooney, S., Nam, Y., Wilcox, A., Park, C., Dowd, F., Williams, K., Grewenow, S.M., Daniel, S., Shankland, S., Pamreddy, A., Ye, H., Montellano, R., Bansal, S., Pillai, A., Zhang, D., Park, H., Patel, J., Sambandam, K., Basit, M., Wen, N., Moe, O.W., Toto, R.D., Lee, S.C., Sharman, K., Caprioli, R.M., Fogo, A., Allen, J., Spraggins, J., Djambazova, K., de, Caestecker, M., Dufresne, M., Farrow, M., Vijayan, A., Minor, B., Nwanne, G., Gaut, J., Conlon, K., Kaushal, M., Diettman, S.M., Victoria, Castro, A.M., Moledina, D., Wilson, F.P., Moeckel, G., Cantley, L., Shaw, M., Kakade, V., Arora, T., Jain, S., Rauchman, M., Eadon, M.T.
المساهمون: University of Arizona
المصدر: Nature Communications
بيانات النشر: Nature Research
سنة النشر: 2024
المجموعة: The University of Arizona: UA Campus Repository
الوصف: There is a need to define regions of gene activation or repression that control human kidney cells in states of health, injury, and repair to understand the molecular pathogenesis of kidney disease and design therapeutic strategies. Comprehensive integration of gene expression with epigenetic features that define regulatory elements remains a significant challenge. We measure dual single nucleus RNA expression and chromatin accessibility, DNA methylation, and H3K27ac, H3K4me1, H3K4me3, and H3K27me3 histone modifications to decipher the chromatin landscape and gene regulation of the kidney in reference and adaptive injury states. We establish a spatially-anchored epigenomic atlas to define the kidney’s active, silent, and regulatory accessible chromatin regions across the genome. Using this atlas, we note distinct control of adaptive injury in different epithelial cell types. A proximal tubule cell transcription factor network of ELF3, KLF6, and KLF10 regulates the transition between health and injury, while in thick ascending limb cells this transition is regulated by NR2F1. Further, combined perturbation of ELF3, KLF6, and KLF10 distinguishes two adaptive proximal tubular cell subtypes, one of which manifested a repair trajectory after knockout. This atlas will serve as a foundation to facilitate targeted cell-specific therapeutics by reprogramming gene regulatory networks. © 2024, The Author(s). ; Open access journal ; This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2041-1723
العلاقة: Gisch, D.L., Brennan, M., Lake, B.B. et al. The chromatin landscape of healthy and injured cell types in the human kidney. Nat Commun 15, 433 (2024). https://doi.org/10.1038/s41467-023-44467-6Test; http://hdl.handle.net/10150/671737Test; Nature Communications
DOI: 10.1038/s41467-023-44467-6
الإتاحة: https://doi.org/10.1038/s41467-023-44467-6Test
http://hdl.handle.net/10150/671737Test
حقوق: © The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License. ; https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.89806A8E
قاعدة البيانات: BASE
الوصف
تدمد:20411723
DOI:10.1038/s41467-023-44467-6