SIRT1 transgenic mice show phenotypes resembling calorie restriction

Summary We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are hemizygous for this transgene express normal levels of β‐actin and higher levels of SIRT1 protein in several tissues. Transgenic mice dis...

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Published inAging cell Vol. 6; no. 6; pp. 759 - 767
Main Authors Bordone, Laura, Cohen, Dena, Robinson, Ashley, Motta, Maria Carla, Van Veen, Ed, Czopik, Agnieszka, Steele, Andrew D., Crowe, Hayley, Marmor, Stephen, Luo, Jianyuan, Gu, Wei, Guarente, Leonard
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.12.2007
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Online AccessGet full text
ISSN1474-9718
1474-9726
1474-9726
DOI10.1111/j.1474-9726.2007.00335.x

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Abstract Summary We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are hemizygous for this transgene express normal levels of β‐actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie‐restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.
AbstractList Summary We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are hemizygous for this transgene express normal levels of β‐actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie‐restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the beta-actin locus. Mice that are hemizygous for this transgene express normal levels of beta-actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie-restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the beta-actin locus. Mice that are hemizygous for this transgene express normal levels of beta-actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie-restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the beta-actin locus. Mice that are hemizygous for this transgene express normal levels of beta-actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie-restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are hemizygous for this transgene express normal levels of β‐actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie‐restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.
Author Van Veen, Ed
Luo, Jianyuan
Cohen, Dena
Motta, Maria Carla
Czopik, Agnieszka
Gu, Wei
Guarente, Leonard
Crowe, Hayley
Marmor, Stephen
Steele, Andrew D.
Bordone, Laura
Robinson, Ashley
Author_xml – sequence: 1
  givenname: Laura
  surname: Bordone
  fullname: Bordone, Laura
– sequence: 2
  givenname: Dena
  surname: Cohen
  fullname: Cohen, Dena
– sequence: 3
  givenname: Ashley
  surname: Robinson
  fullname: Robinson, Ashley
– sequence: 4
  givenname: Maria Carla
  surname: Motta
  fullname: Motta, Maria Carla
– sequence: 5
  givenname: Ed
  surname: Van Veen
  fullname: Van Veen, Ed
– sequence: 6
  givenname: Agnieszka
  surname: Czopik
  fullname: Czopik, Agnieszka
– sequence: 7
  givenname: Andrew D.
  surname: Steele
  fullname: Steele, Andrew D.
– sequence: 8
  givenname: Hayley
  surname: Crowe
  fullname: Crowe, Hayley
– sequence: 9
  givenname: Stephen
  surname: Marmor
  fullname: Marmor, Stephen
– sequence: 10
  givenname: Jianyuan
  surname: Luo
  fullname: Luo, Jianyuan
– sequence: 11
  givenname: Wei
  surname: Gu
  fullname: Gu, Wei
– sequence: 12
  givenname: Leonard
  surname: Guarente
  fullname: Guarente, Leonard
BackLink https://www.ncbi.nlm.nih.gov/pubmed/17877786$$D View this record in MEDLINE/PubMed
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Snippet Summary We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that...
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are...
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the beta-actin locus. Mice that are...
We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the beta -actin locus. Mice that are...
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StartPage 759
SubjectTerms Adipokines - blood
Animals
Blood Glucose - analysis
Caloric Restriction
calorie restriction
Cholesterol - blood
Insulin - blood
Longevity - genetics
Mice
Mice, Transgenic
Phenotype
SIRT1
Sirtuin 1
Sirtuins - genetics
Sirtuins - metabolism
transgenic mice
Up-Regulation
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  providerName: Wiley-Blackwell
Title SIRT1 transgenic mice show phenotypes resembling calorie restriction
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1474-9726.2007.00335.x
https://www.ncbi.nlm.nih.gov/pubmed/17877786
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Volume 6
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