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Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes. / Sharoyko, Vladimir V.; Abels, Mia; Sun, Jiangming; Nicholas, Lisa M.; Mollet, Ines Guerra; Stamenkovic, Jelena A.; Göhring, Isabel; Malmgren, Siri; Storm, Petter; Fadista, Joaõ; Spégel, Peter; Metodiev, Metodi D.; Larsson, Nils Göran5; Eliasson, Lena; Wierup, Nils; Mulder, Hindrik.

In: Human Molecular Genetics, Vol. 23, No. 21, 01.11.2014, p. 5733-5749.

Research output: Contribution to journalArticlepeer-review

Harvard

Sharoyko, VV, Abels, M, Sun, J, Nicholas, LM, Mollet, IG, Stamenkovic, JA, Göhring, I, Malmgren, S, Storm, P, Fadista, J, Spégel, P, Metodiev, MD, Larsson, NG, Eliasson, L, Wierup, N & Mulder, H 2014, 'Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes', Human Molecular Genetics, vol. 23, no. 21, pp. 5733-5749. https://doi.org/10.1093/hmg/ddu288

APA

Sharoyko, V. V., Abels, M., Sun, J., Nicholas, L. M., Mollet, I. G., Stamenkovic, J. A., Göhring, I., Malmgren, S., Storm, P., Fadista, J., Spégel, P., Metodiev, M. D., Larsson, N. G., Eliasson, L., Wierup, N., & Mulder, H. (2014). Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes. Human Molecular Genetics, 23(21), 5733-5749. https://doi.org/10.1093/hmg/ddu288

Vancouver

Sharoyko VV, Abels M, Sun J, Nicholas LM, Mollet IG, Stamenkovic JA et al. Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes. Human Molecular Genetics. 2014 Nov 1;23(21):5733-5749. https://doi.org/10.1093/hmg/ddu288

Author

Sharoyko, Vladimir V. ; Abels, Mia ; Sun, Jiangming ; Nicholas, Lisa M. ; Mollet, Ines Guerra ; Stamenkovic, Jelena A. ; Göhring, Isabel ; Malmgren, Siri ; Storm, Petter ; Fadista, Joaõ ; Spégel, Peter ; Metodiev, Metodi D. ; Larsson, Nils Göran5 ; Eliasson, Lena ; Wierup, Nils ; Mulder, Hindrik. / Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes. In: Human Molecular Genetics. 2014 ; Vol. 23, No. 21. pp. 5733-5749.

BibTeX

@article{3504e44515e04fb5a7b032a1a52c0c00,
title = "Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes",
abstract = "Wehave previously identifiedtranscription factorB1mitochondrial (TFB1M)as a type 2 diabetes (T2D) risk gene, using human and mouse genetics. To further understand the function of TFB1M and how it is associated with T2D, we created a b-cell-specific knockout of Tfb1m, which gradually developed diabetes. Prior to the onset of diabetes, b-Tfb1m2/2 mice exhibited retarded glucose clearance owing to impaired insulin secretion. b-Tfb1m2/2 islets released less insulin in response to fuels, contained less insulin and secretory granules and displayed reduced b-cell mass. Moreover, mitochondria in Tfb1m-deficient b-cells were more abundant with disrupted architecture. TFB1M is known to control mitochondrial protein translation by adenine dimethylation of 12S ribosomalRNA(rRNA). Here,wefound that the levels ofTFB1Mand mitochondrial-encoded proteins, mitochondrial 12S rRNA methylation, ATP production and oxygen consumption were reduced in b-Tfb1m2/2 islets. Furthermore, the levels of reactive oxygen species (ROS) in response to cellular stress were increased whereas induction of defense mechanisms was attenuated. We also show increased apoptosis and necrosis as well as infiltration of macrophages and CD41 cells in the islets. Taken together, our findings demonstrate that Tfb1m-deficiency in b-cells caused mitochondrial dysfunction and subsequently diabetes owing to combined loss of b-cell function and mass. These observations reflect pathogenetic processes in human islets: using RNA sequencing, we found that the TFB1M risk variant exhibited a negative gene-dosage effect on islet TFB1M mRNA levels, as well as insulin secretion. Our findings highlight the role of mitochondrial dysfunction in impairments of b-cell function and mass, the hallmarks of T2D.",
author = "Sharoyko, {Vladimir V.} and Mia Abels and Jiangming Sun and Nicholas, {Lisa M.} and Mollet, {Ines Guerra} and Stamenkovic, {Jelena A.} and Isabel G{\"o}hring and Siri Malmgren and Petter Storm and Joa{\~o} Fadista and Peter Sp{\'e}gel and Metodiev, {Metodi D.} and Larsson, {Nils G{\"o}ran5} and Lena Eliasson and Nils Wierup and Hindrik Mulder",
year = "2014",
month = nov,
day = "1",
doi = "10.1093/hmg/ddu288",
language = "English",
volume = "23",
pages = "5733--5749",
journal = "Human Molecular Genetics",
issn = "0964-6906",
publisher = "Oxford University Press",
number = "21",

}

RIS

TY - JOUR

T1 - Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes

AU - Sharoyko, Vladimir V.

AU - Abels, Mia

AU - Sun, Jiangming

AU - Nicholas, Lisa M.

AU - Mollet, Ines Guerra

AU - Stamenkovic, Jelena A.

AU - Göhring, Isabel

AU - Malmgren, Siri

AU - Storm, Petter

AU - Fadista, Joaõ

AU - Spégel, Peter

AU - Metodiev, Metodi D.

AU - Larsson, Nils Göran5

AU - Eliasson, Lena

AU - Wierup, Nils

AU - Mulder, Hindrik

PY - 2014/11/1

Y1 - 2014/11/1

N2 - Wehave previously identifiedtranscription factorB1mitochondrial (TFB1M)as a type 2 diabetes (T2D) risk gene, using human and mouse genetics. To further understand the function of TFB1M and how it is associated with T2D, we created a b-cell-specific knockout of Tfb1m, which gradually developed diabetes. Prior to the onset of diabetes, b-Tfb1m2/2 mice exhibited retarded glucose clearance owing to impaired insulin secretion. b-Tfb1m2/2 islets released less insulin in response to fuels, contained less insulin and secretory granules and displayed reduced b-cell mass. Moreover, mitochondria in Tfb1m-deficient b-cells were more abundant with disrupted architecture. TFB1M is known to control mitochondrial protein translation by adenine dimethylation of 12S ribosomalRNA(rRNA). Here,wefound that the levels ofTFB1Mand mitochondrial-encoded proteins, mitochondrial 12S rRNA methylation, ATP production and oxygen consumption were reduced in b-Tfb1m2/2 islets. Furthermore, the levels of reactive oxygen species (ROS) in response to cellular stress were increased whereas induction of defense mechanisms was attenuated. We also show increased apoptosis and necrosis as well as infiltration of macrophages and CD41 cells in the islets. Taken together, our findings demonstrate that Tfb1m-deficiency in b-cells caused mitochondrial dysfunction and subsequently diabetes owing to combined loss of b-cell function and mass. These observations reflect pathogenetic processes in human islets: using RNA sequencing, we found that the TFB1M risk variant exhibited a negative gene-dosage effect on islet TFB1M mRNA levels, as well as insulin secretion. Our findings highlight the role of mitochondrial dysfunction in impairments of b-cell function and mass, the hallmarks of T2D.

AB - Wehave previously identifiedtranscription factorB1mitochondrial (TFB1M)as a type 2 diabetes (T2D) risk gene, using human and mouse genetics. To further understand the function of TFB1M and how it is associated with T2D, we created a b-cell-specific knockout of Tfb1m, which gradually developed diabetes. Prior to the onset of diabetes, b-Tfb1m2/2 mice exhibited retarded glucose clearance owing to impaired insulin secretion. b-Tfb1m2/2 islets released less insulin in response to fuels, contained less insulin and secretory granules and displayed reduced b-cell mass. Moreover, mitochondria in Tfb1m-deficient b-cells were more abundant with disrupted architecture. TFB1M is known to control mitochondrial protein translation by adenine dimethylation of 12S ribosomalRNA(rRNA). Here,wefound that the levels ofTFB1Mand mitochondrial-encoded proteins, mitochondrial 12S rRNA methylation, ATP production and oxygen consumption were reduced in b-Tfb1m2/2 islets. Furthermore, the levels of reactive oxygen species (ROS) in response to cellular stress were increased whereas induction of defense mechanisms was attenuated. We also show increased apoptosis and necrosis as well as infiltration of macrophages and CD41 cells in the islets. Taken together, our findings demonstrate that Tfb1m-deficiency in b-cells caused mitochondrial dysfunction and subsequently diabetes owing to combined loss of b-cell function and mass. These observations reflect pathogenetic processes in human islets: using RNA sequencing, we found that the TFB1M risk variant exhibited a negative gene-dosage effect on islet TFB1M mRNA levels, as well as insulin secretion. Our findings highlight the role of mitochondrial dysfunction in impairments of b-cell function and mass, the hallmarks of T2D.

UR - http://www.scopus.com/inward/record.url?scp=84911361474&partnerID=8YFLogxK

U2 - 10.1093/hmg/ddu288

DO - 10.1093/hmg/ddu288

M3 - Article

C2 - 24916378

VL - 23

SP - 5733

EP - 5749

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 21

ER -

ID: 5715990