The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Control of Mitochondrial Transcription Specificity Factors (TFB1M and TFB2M) by Nuclear Respiratory Factors (NRF-1 and NRF-2) and PGC-1 Family Coactivators
Open accessAbstract
In vertebrates, mitochondrial DNA (mtDNA) transcription is initiated bidirectionally from closely spaced promoters, HSP and LSP, within the D-loop regulatory region. Early studies demonstrated that mtDNA transcription requires mitochondrial RNA polymerase and Tfam, a DNA binding stimulatory factor that is required for mtDNA maintenance. Recently, mitochondrial transcription specificity factors (TFB1M and TFB2M), which markedly enhance mtDNA transcription in the presence of Tfam and mitochondrial RNA polymerase, have been identified in mammalian cells. Here, we establish that the expression of human TFB1M and TFB2M promoters is governed by nuclear respiratory factors (NRF-1 and NRF-2), key transcription factors implicated in mitochondrial biogenesis. In addition, we show that NRF recognition sites within both TFB promoters are required for maximal trans activation by the PGC-1 family coactivators, PGC-1alpha and PRC. The physiological induction of these coactivators has been associated with the integration of NRFs and other transcription factors in a program of mitochondrial biogenesis. Finally, we demonstrate that the TFB genes are up-regulated along with Tfam and either PGC-1alpha or PRC in cellular systems where mitochondrial biogenesis is induced. Moreover, ectopic expression of PGC-1alpha is sufficient to induce the coordinate expression of all three nucleus-encoded mitochondrial transcription factors along with nuclear and mitochondrial respiratory subunits. These results support the conclusion that the coordinate regulation of nucleus-encoded mitochondrial transcription factors by NRFs and PGC-1 family coactivators is essential to the control of mitochondrial biogenesis.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Key in orchestrating this process is the nuclear-encoded mitochondrial transcription factor A (TFAM), which is pivotal in regulating mtDNA transcription by directly interacting with mitochondrial genome along with mitochondrial transcription specificity factors TFB1M and TFB2M (Figure 3; Gleyzer et al., 2005; Ljubicic et al., 2010).”
From Mitochondrial (Dys)function and Insulin Resistance: From Pathophysiological Molecular Mechanisms to the Impact of Diet (2019) · cites this paper as Gleyzer et al., 2005
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
PCR protocols — A guide to methods and applications
U.G. (1990) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(90)90252-7 · Cited by 11,751
Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139
Andrews, N. C., & Faller, D. V. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.9.2499 · Cited by 2,292
Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076
Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice
Larsson, N.-G., Wang, J., Wilhelmsson, H., Oldfors, A., Rustin, P., Lewandoski, M., Barsh, G. S., & Clayton, D. A. (1998) · Nature Genetics · doi:10.1038/ng0398-231 · Cited by 1,594
Peroxisome proliferator–activated receptor γ coactivator-1 promotes cardiac mitochondrial biogenesis
Lehman, J. J., Barger, P. M., Kovacs, A., Saffitz, J. E., Medeiros, D. M., & Kelly, D. P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10268 · Cited by 1,285
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function
Kelly, D. P., & Scarpulla, R. C. (2004) · Genes & Development · doi:10.1101/gad.1177604 · Cited by 1,243
Vega, R. B., Huss, J. M., & Kelly, D. P. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.5.1868-1876.2000 · Cited by 1,195
MITOCHONDRIAL DNA MAINTENANCE IN VERTEBRATES
Shadel, G. S., & Clayton, D. A. (1997) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.66.1.409 · Cited by 1,059
Virbasius, J. V., & Scarpulla, R. C. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.4.1309 · Cited by 819
Cited by
Sorted by citations
Items 501–600 of 709
ULP-2 SUMO protease regulates UPRmt and mitochondrial homeostasis in Caenorhabditis elegans
Michaeli, L., Spector, E., Haeussler, S., Carvalho, C. A., Grobe, H., Abu‐Shach, U. B., Zinger, H., Conradt, B., & Broday, L. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.01.050 · Cited by 9
Cellular Mechanisms of Drug Nephrotoxicity
Walker, R. J., & Endre, Z. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381462-3.00085-9 · Cited by 8
Metabolic Signaling as a Driver of T Cell Aging
Choi, M. S., Choi, S., Cho, M., & Kim, C. (2025) · Immune Network · doi:10.4110/in.2025.25.e14 · Cited by 8
Zhao, H., Huang, H.-W., Wu, J., & Huang, P.-Y. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.06.014 · Cited by 7
Zeng, X., Liu, D., Han, Y. Y., Huang, Z., Zhang, J., & Huang, Q. (2020) · PubMed Central · Cited by 7
Rivera, M. E., Rivera, C. N., & Vaughan, R. A. (2021) · Endocrine · doi:10.1007/s12020-021-02939-z · Cited by 7
Mitochondrial Metabolism and Insulin Action
Turner, N. A. (2013) · InTech eBooks · doi:10.5772/56449 · Cited by 8
Han, Y., & Xin, Y. (2013) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.1000-9604.2013.11.11 · Cited by 7
Rivera, C. N., Hinkle, J. S., Watne, R. M., Macgowan, T. C., Wommack, A. J., & Vaughan, R. A. (2023) · PPAR Research · doi:10.1155/2023/4779199 · Cited by 7
Shimura, T., Sunaga, K., Yamazaki, M., Honoka, N., Sasatani, M., Kamiya, K., & Ushiyama, A. (2024) · International Journal of Radiation Biology · doi:10.1080/09553002.2023.2295297 · Cited by 6
Mitochondrial Imbalance in Down Syndrome: A Driver of Accelerated Brain Aging?
Zuo, X. (2025) · Aging and Disease · doi:10.14336/ad.2025.0189 · Cited by 9
Hao, Y., Chen, F., Ren, X., Huang, X., & Zhou, X. (2025) · Genes & Diseases · doi:10.1016/j.gendis.2025.101645 · Cited by 7
Sekiya, F. S., da Silva, C. P. N., Oba‐Shinjo, S. M., Santos‐Bezerra, D. P., Ravagnani, F. G., Pasqualucci, C. A., Gil, S. D. S., Gualano, B., Baptista, M. S., Corrêa‐Giannella, M. L., et al. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111932 · Cited by 6
Metabolically Relevant Cell Biology – Role of Intracellular Organelles for Cardiac Metabolism
Niemann, B., & Rohrbach, S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802394-5.00003-0 · Cited by 9
Khodagholi, F., Shahamati, S. Z., Chamgordani, M. M., Mousavi, M. A., Moslemi, M., Salehpour, M., Rafiei, S., & Foolad, F. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06177-4 · Cited by 6
Ziemann, M., Wu, W., Deng, X., & Du, X. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.921610 · Cited by 6
Exercise-Induced Mitochondrial Biogenesis in Skeletal Muscle
Hood, D. A., Chabi, B., Menzies, K. J., O′Leary, M. F. N., & Walkinshaw, D. R. (2007) · Springer eBooks · doi:10.1007/978-88-470-0376-7_3 · Cited by 6
Dykens, J. A. (2007) · Elsevier eBooks · doi:10.1016/b0-08-045044-x/00071-7 · Cited by 6
Zhang, L., Pouya, A., Kopetzky, J., Bitar, S., Wolf, C., Bello, F. D., Gomez‐Zepeda, D., Tenzer, S., & Methner, A. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107019 · Cited by 5
Mitochondrial transplant: Unravelling a promising treatment for ocular diseases
Yeo, Y., Bhargava, M., Khare, R. S., Parikh, B. H., & Su, X. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103902 · Cited by 6
Repression of the transcriptional activity of ERRα with sequence-specific DNA-binding polyamides
Chen, C.-Y., Li, Y., Jia, T., He, L., Hare, A. A., Silberstein, A. L., Gallagher, J., Martinez, T. F., Stiles, J. W., Olenyuk, B. Z., et al. (2020) · Medicinal Chemistry Research · doi:10.1007/s00044-019-02493-4 · Cited by 5
Liang, Y., Gu, M., Xiao, L., Zhou, Y., Yang, Q., Wang, Z., Yao, W., Gao, X., & Chen, S. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113684 · Cited by 5
Lesions of the mitochondrial genome and ways of its preservation
Gasiev, A. I., & Shaikhaev, G. O. (2008) · Russian Journal of Genetics · doi:10.1134/s1022795408040017 · Cited by 5
Seene, T., Kaasik, P., & Seppet, E. K. (2017) · Health · doi:10.4236/health.2017.95056 · Cited by 6
Mitochondrial Biogenesis and Dynamics in Health and Disease
Campos, J. C., Bozi, L. H. M., & Ferreira, J. C. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-86684-6_3 · Cited by 4
Ma, S., He, L., Zuo, Q., Zhang, G., & Guo, Y. (2023) · Cardiovascular Innovations and Applications · doi:10.15212/cvia.2022.0024 · Cited by 5
Kang, S. Y., Hyun, S. Y., Kwon, Y., Park, Y.-K., & Jung, H. W. (2019) · The Korea Journal of Herbology · doi:10.6116/kjh.2019.34.6.99 · Cited by 5
Transcription and its regulation in mammalian and human mitochondria
Sologub, M., Kochetkov, S. N., & Temiakov, D. (2009) · Molecular Biology · doi:10.1134/s0026893309020034 · Cited by 5
The Potential Use of PGC-1α and PGC-1β to Protect the Retina by Stimulating Mitochondrial Repair
Abrahan, C. E., & Ash, J. D. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-17121-0_53 · Cited by 5
Evaluating the role of NRF-1 in regulation of the goldfish COX4-1 gene in response to temperature
Gao, G., & Moyes, C. D. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.141184 · Cited by 5
Mitochondrial Proteins in the Development of Parkinson’s Disease
Zilocchi, M., Fasano, M., & Alberio, T. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-8367-0_2 · Cited by 5
Nikolić, N., Bakke, S. S., Kase, E. T., Rudberg, I., Halle, I. F., Rustan, A. C., Thoresen, G. H., & Aas, V. (2013) · PLoS ONE · doi:10.1371/annotation/270b432d-50ec-41f1-ad4d-ddd9f51f62a5 · Cited by 5
Hushmandi, K., Salarizadeh, N., Einollahi, B., Izadi, M., Doosti, P., Behzadnia, M. J., Cho, W. C., Yousefi, T., Khoshnazar, S. M., Alimohammadi, M., et al. (2026) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-025-01824-0 · Cited by 4
Li, J., Liang, R., Mao, Y., Yang, X., Luo, X., Zhu, L., & Zhang, Y. (2026) · Meat Science · doi:10.1016/j.meatsci.2026.110112 · Cited by 4
Qianyang yuyin granule ameliorates mitochondrial dysfunction of hypertensive myocardial remodeling
Zheng, Y., Fang, Y., Luo, Y., Fang, Z., & Fang, Z. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118610 · Cited by 4
Zhang, C.-X., Chang, X., Zhao, D., He, Y., Dong, G., & Gao, L. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1536773 · Cited by 6
Fiorani, M., Buffi, G., Bagherlou, N., Canonico, B., de Matteis, R., Guidarelli, A., Montanari, M., Battistelli, M., Papa, S., Coppo, L., et al. (2025) · Biochimica et biophysica acta. Molecular cell research · doi:10.1016/j.bbamcr.2025.119967 · Cited by 6
Xiao, Y., Xu, C., Chen, Z., Dai, W., Hu, X., Zhang, S., Zhong, J., Chen, J., Liu, X., Liang, L., et al. (2024) · Aging Cell · doi:10.1111/acel.14319 · Cited by 4
Exploring mitochondrial dynamics and localization under cellular stress: A comprehensive insight
Agarwal, S., Karuppusamy, K. A., & Gupta, A. K. (2025) · Journal of Biosciences · doi:10.1007/s12038-025-00514-6 · Cited by 4
Chronic stress elicits sex‐specific mitochondrial respiratory functional changes in the rat heart
Odendaal, C., O'Brien, C., Cairns, M., Maarman, G. J., Joseph, D. E., Smith, C., Rautenbach, F., Marnewick, J. L., & Essop, M. F. (2025) · Physiological Reports · doi:10.14814/phy2.70371 · Cited by 4
The Effects of Astragali Radix Extracts on Mitochondrial Function in C2C12 Myotubes
Song, M. (2014) · Journal of Korean Medicine for Obesity Research · doi:10.15429/jkomor.2014.14.2.55 · Cited by 4
Verma, G., & Rico, S. G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817193-6.00008-x · Cited by 4
Miyanishi, H., Kitazawa, A., Izuo, N., Muramatsu, S., & Nitta, A. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03594-0 · Cited by 3
Mitochondrial physiology: An overview
Infantino, V., Todisco, S., & Convertini, P. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-88462-4.00001-8 · Cited by 5
Durán, A., Priestman, D. A., Heras, M. L., Rebolledo‐Jaramillo, B., Olguín, V., Calderón, J. F., Zanlungo, S., Gutiérrez, J., Platt, F. M., & Klein, A. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054915 · Cited by 4
Transcriptional Control of Striated Muscle Mitochondrial Biogenesis and Function
Kelly, D. P., & Scarpulla, R. C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381510-1.00016-8 · Cited by 4
Lee, T.-Y., Tsai, K., Lee, W.-S., & Hsu, C. (2007) · Journal of Molecular Endocrinology · doi:10.1677/jme.1.00002 · Cited by 4
Vertebrates show coordinated elevated expression of mitochondrial and nuclear genes after birthPreprint
Medini, H., & Mishmar, D. (2025) · Genome Research · doi:10.1101/gr.279700.124 · Cited by 4
Effect of mTORC Agonism via MHY1485 with and without Rapamycin on C2C12 Myotube Metabolism
Cook, N. E., McGovern, M. R., Zaman, T., Lundin, P. M., & Vaughan, R. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136819 · Cited by 6
Dietary cannabidiol oil mitigates metabolic dysfunction in mice with high-fat diet-induced obesity
Iniguez, A. B., Sun, Q., Tian, Q., Du, ., & Zhu, M. J. (2025) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2025.110040 · Cited by 3
Lee, T. W., Bae, E., Kim, J. H., Jung, M. H., & Park, D. J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178353 · Cited by 3
Traumatic Skeletal Muscle Injury and Recovery
Greising, S. M., Call, J. A., & Baumann, C. W. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-88361-3_10 · Cited by 4
Pan, X., Mowdawalla, C., Bagnato, S., Pessin, J. E., Vallon, V., & Hussain, M. M. (2025) · Nature Communications · doi:10.1038/s41467-025-65402-x · Cited by 3
Luo, J., Lu, F., Cuciureanu, M. D., Xu, X., Dong, H., & Gong, M. (2026) · Renal Failure · doi:10.1080/0886022x.2026.2620218 · Cited by 3
Rios, W. Q., Silva, C. M., Ferreira, R. M., & Gomes, J. R. B. (2026) · Journal of Molecular Medicine · doi:10.1007/s00109-026-02694-6 · Cited by 3
Epicatechin promotes oocyte quality in mice during repeated superovulation
Feng, Y., Wu, Z., Zhao, X., Chen, M., Li, S., Lu, C., Shi, D., & Lu, F. (2023) · Theriogenology · doi:10.1016/j.theriogenology.2023.06.025 · Cited by 3
Gavrilova, D., Bezsonov, E. E., & Degtyarevskaya, T. (2023) · Journal of Translational Genetics and Genomics · doi:10.20517/jtgg.2023.38 · Cited by 4
Luján, L. M. L., McCarty, M. F., Galvez-Ruiz, J. C., López, S. T., & Assanga, S. B. I. (2024) · Human Nutrition & Metabolism · doi:10.1016/j.hnm.2024.200281 · Cited by 2
Makwana, K., Velazquez, E. J., Marzese, D. M., Smith, B., Bhowmick, N. A., Faries, M. B., Hamid, O., & Boiko, A. D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1495032 · Cited by 3
Chen, S., Cao, Y., Fan, Z., Xu, L., Pan, Z., Gao, Y., Wei, L., Wei, Q., Tian, Y., Zhang, X., et al. (2024) · Molecular Medicine · doi:10.1186/s10020-024-01017-0 · Cited by 4
Wang, J., Liu, P., Tan, T., Zhang, M., Xi, B., Li, D., & Wu, L. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.743065 · Cited by 3
Travis, K. B., Ragland, K. J., Spry, E. R., Zaman, T., Lundin, P. M., & Vaughan, R. A. (2025) · Acta Diabetologica · doi:10.1007/s00592-025-02570-8 · Cited by 3
Role of transcription factors in mtDNA biogenesis mediated by thyroid hormones
Patrushev, M. V., & Patrusheva, V. E. (2011) · Biochemistry (Moscow) · doi:10.1134/s0006297911020131 · Cited by 3
The Role and Regulation of PGC-1α and PGC-1β in Skeletal Muscle Adaptation
Lamon, S., & Russell, A. P. (2017) · Springer eBooks · doi:10.1007/978-981-10-3292-9_8 · Cited by 3
Metabolic Syndrome, Hormones, and Exercise
Δίπλα, Κ., Zafeiridis, A., & Tordjman, K. M. (2020) · Contemporary Endocrinology · doi:10.1007/978-3-030-33376-8_29 · Cited by 3
Guo, J., Ye, X., Zhao, Y., Huang, D., Wu, Q., Ihsan, A., & Wang, X. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113687 · Cited by 4
Lee, H., Ye, S., Kim, J., Jun, S., & Kang, N. G. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46060302 · Cited by 3
Morrish, F. M., Gingras, H., Noonan, J., Huang, L., Sweet, I. R., Kuok, I. T., Knoblaugh, S. E., & Hockenbery, D. M. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.150478 · Cited by 3
Yiş, U., Ezgü, F. S., Karakaya, P., Polat, İ., Arslan, N., Çankaya, T., Bozkaya, Ö. G., & Kurul, S. H. (2014) · Journal of Child Neurology · doi:10.1177/0883073814530499 · Cited by 3
Activity-Dependent Bigenomic Transcriptional Regulation of Cytochrome c Oxidase in Neurons
Wong‐Riley, M. T. T., Liang, H., & Ongwijitwat, S. (2007) · Springer eBooks · doi:10.1007/978-0-387-73609-9_11 · Cited by 3
The Molecular Genetics of Oogenesis
Zhai, F., Ma, X., Yan, L., & Qiao, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813570-9.00007-3 · Cited by 4
Zhang, W., Xiong, H., Pang, J., Lai, L., Su, Z., Lin, H., Jian, B., Yang, H., & Zheng, Y. (2019) · Journal of Bio-X Research · doi:10.1097/jbr.0000000000000038 · Cited by 3
Ji, L., Huang, B., Ren, D., Wei, X., Liu, L., Bi, Y., Li, Z., Yuan, F., Han, K. Q., Li, K., et al. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70275 · Cited by 2
Xie, X., Yu, T., Deng, W., & Xie, S. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108106 · Cited by 4
Fu, W., Wang, J., Guo, Z., Ong, S., Gao, Y., Zhu, H., Wang, J., Du, Z., Meng, M., & Chang, X. (2026) · Acta Diabetologica · doi:10.1007/s00592-026-02706-4 · Cited by 2
7.3 Transcriptional Integration of Mitochondrial Biogenesis
Scarpulla, R. C. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_29 · Cited by 2
The potential role of environmental factors in modulating mitochondrial DNA epigenetic marks
Ryva, B. A., Zhou, Z., Goodrich, J. M., & Strakovsky, R. S. (2023) · Vitamins and hormones · doi:10.1016/bs.vh.2023.01.011 · Cited by 2
Rivera, C. N., Kamer, M. M., Cook, N. E., McGovern, M. R., Watne, R. M., Wommack, A., & Vaughan, R. (2023) · Cell Biochemistry and Function · doi:10.1002/cbf.3878 · Cited by 3
Wang, Q., Zeng, Z., Guo, L., Williams, K. E., Zhang, Y., Tang, H., Hu, H., Qin, G., Wang, K., & Wang, X. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1531302 · Cited by 2
Key Transcription Factors: Avenue for Treating Alcoholic Liver Disease
Guo, M., Cao, J.-N., Li, X., & Jin, L. (2025) · Current Medical Science · doi:10.1007/s11596-025-00079-3 · Cited by 2
Skeletal Muscle Mitochondrial Function/Dysfunction and Type 2 Diabetes
González-Franquesa, A., De, V., Lerín, C., & Pablo, M. (2012) · InTech eBooks · doi:10.5772/50130 · Cited by 3
Seppet, E. K., Orlova, E., Seene, T., & Gellerich, F. N. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5203-4_20 · Cited by 2
Mitochondrial biogenesis and mitophagy
Tan, S., Kennedy, B. K., & Wong, E. S. P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821562-3.00037-x · Cited by 2
Rivera, M. E., & Vaughan, R. A. (2021) · Lipids · doi:10.1002/lipd.12315 · Cited by 3
The molecular genetics of oogenesis
Zhai, F., Ma, X., Yan, L., & Qiao, J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91380-5.00011-3 · Cited by 2
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the BrainPreprint
Liu, S., Aldinger, K. A., Cheng, C. V., Kiyama, T., Dave, M., McNamara, H. K., Caraffi, S. G., Ivanovski, I. P., Errichiello, E., Zweier, C., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.30.437620 · Cited by 2
Excess glutamine does not alter myotube metabolism or insulin sensitivity
Krone, M. J., Rivera, C. N., Rivera, M. E., Watne, R. M., Lemonds, S. E., Wommack, A. J., & Vaughan, R. A. (2022) · Amino Acids · doi:10.1007/s00726-022-03131-x · Cited by 1
Xie, Z., Pu, Y., Yi, H., Feng, L., Zhang, Y., Zhou, P., Diao, H., & Yan, H. (2025) · Journal of Agriculture and Food Research · doi:10.1016/j.jafr.2025.102356 · Cited by 1
Mitochondrial DNA homeostasis: A novel therapeutic target for neurodegenerative diseases
Fu, T., Chen, X., Zhang, S., Fu, Y., Huang, L., & Xiong, W. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-00495 · Cited by 1
Schmid, K., Schenk, R. P., & Wiedemann, G. M. (2025) · European Journal of Immunology · doi:10.1002/eji.70066 · Cited by 1
Ganguly, A., Carter, C. M., Negron, A. R., Zhong, H., Moreira, A. G., Walters, M. S., Rogers, L. K., Prakash, Y. S., Tipple, T. E., & Richardson, A. (2025) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00205.2025 · Cited by 1
TOM70-Mitochondrial Pathway Reduction Mediates DEHP-Induced Neuroinflammation in Mice
Zhu, H.-M., Chen, M., Saleem, M. A. U., Wang, J.-X., Jiang, F.-W., Liu, S., Shi, Y.-S., Zhao, Y., & Li, J. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c09700 · Cited by 1
Xi, S., Ma, J., Yan, J., Li, Y., Zhang, P., Chen, H., Yang, G., Fu, X., Liu, J., & Zhang, Y. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1746901 · Cited by 6
Li, P., Gao, J., Li, H.-H., & Jiang, W. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153387 · Cited by 1
A Function-Centric Framework for Mitochondrial Quality Control
Ozcan, F., Vujovic, F., & Farahani, R. H. (2026) · Biomolecules · doi:10.3390/biom16081116 · Cited by 1
6.5 Mitochondrial Mechanisms of Oxidative Stress and Apoptosis
Soane, L., Solenski, N. J., & Fiskum, G. M. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_26 · Cited by 1
Belgrave, K. R. (2012) · Scholarship@Western (Western University) · Cited by 1
Transcriptional Control of Mitochondrial Biogenesis and Maturation
Vega, R. B., Leone, T. C., & Kelly, D. P. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1227-8_6 · Cited by 1
Aberrant increase in cytochrome c oxidase subunit I precedes neuronal death after cerebral ischemia
Takahashi, Y., Sugawara, T., Miyazaki, T., Itoh, H., & Mizoi, K. (2013) · Neuroreport · doi:10.1097/wnr.0000000000000018 · Cited by 1
Poberezhnyi, V. I., Marchuk, O., Shvidyuk, O. S., Petrik, I., & Logvinov, O. S. (2019) · Pain medicine · doi:10.31636/pmjua.v3i4.1 · Cited by 1
Metadata
- Authors
- Gleyzer, N., Vercauteren, K., & Scarpulla, R. C.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Scarpulla, Richard C.
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2005-02-01
- Volume
- 25
- Issue
- 4
- Pages
- 1354-1366
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC548005
- OpenAlex
- W2158088166
- Cited by
- 711
- References
- 39
- Citations by year
- 2026: 26 · 2025: 44 · 2024: 38 · 2023: 46 · 2022: 45 · 2021: 40 · 2020: 40 · 2019: 39 · 2018: 43 · 2017: 27 · 2016: 27 · 2015: 34 · 2014: 22 · 2013: 33 · 2012: 32
- FWCI
- 10.08
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Biology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service
- National Institute of General Medical Sciences (GM32525-22, R56GM032525, R01GM032525)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- TFB1M, TFB2M, nuclear respiratory factors, NRF1, Nrf2, PGC-1α, mitochondrial biogenesis, mitochondrial transcription, TFAM, transcriptional regulation, mitochondrial RNA polymerase
- MeSH terms
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Animals, Base Sequence, DNA-Binding Proteins, DNA, Mitochondrial, High Mobility Group Proteins, Humans, Methyltransferases, Molecular Sequence Data, Nuclear Proteins, Promoter Regions, Genetic, Transcription Factors, Trans-Activators, Up-Regulation, Mitochondrial Proteins, Electrophoretic Mobility Shift Assay, BALB 3T3 Cells, 3T3-L1 Cells, Nuclear Respiratory Factors, NF-E2-Related Factor 1, Nuclear Respiratory Factor 1, NF-E2-Related Factor 2, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review