Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily

Christine Rossmann; Christian Windpassinger; Daniela Brunner; Alenka Kovacevic; Natascha Schweighofer; Roland Malli; Rufina Schuligoi; Andreas Prokesch; Barbara Kluve-Beckerman; Wolfgang F. Graier; Dagmar Kratky; Wolfgang Sattler; Ernst Malle

doi:10.1016/j.bbrc.2014.07.054

Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily

Christine Rossmann, Christian Windpassinger, Daniela Brunner, Alenka Kovacevic, Natascha Schweighofer, Roland Malli, Rufina Schuligoi, Andreas Prokesch, Barbara Kluve-Beckerman, Wolfgang F. Graier, Dagmar Kratky, Wolfgang Sattler, Ernst Malle^*

^*Corresponding author for this work

Institute of Biochemistry (6480)

Research output: Contribution to journal › Article › peer-review

Abstract

The serum amyloid A (SAA) family of proteins is encoded by multiple genes, which display allelic variation and a high degree of homology in mammals. The SAA1/2 genes code for non-glycosylated acute-phase SAA1/2 proteins, that may increase up to 1000-fold during inflammation. The SAA4 gene, well characterized in humans (hSAA4) and mice (mSaa4) codes for a SAA4 protein that is glycosylated only in humans. We here report on a previously uncharacterized SAA4 gene (rSAA4) and its product in Rattus norvegicus, the only mammalian species known not to express acute-phase SAA. The exon/intron organization of rSAA4 is similar to that reported for hSAA4 and mSaa4. By performing 5′- and 3′RACE, we identified a 1830-bases containing rSAA4 mRNA (including a GA-dinucleotide tandem repeat). Highest rSAA4 mRNA expression was detected in rat liver. In McA-RH7777 rat hepatoma cells, rSAA4 transcription was significantly upregulated in response to LPS and IL-6 while IL-1α/β and TNFα were without effect. Luciferase assays with promoter-truncation constructs identified three proximal C/EBP-elements that mediate expression of rSAA4 in McA-RH7777 cells. In line with sequence prediction a 14-kDa non-glycosylated SAA4 protein is abundantly expressed in rat liver. Fluorescence microscopy revealed predominant localization of rSAA4-GFP-tagged fusion protein in the ER.

Original language	English
Pages (from-to)	1643-1649
Number of pages	7
Journal	Biochemical and Biophysical Research Communications
Volume	450
Issue number	4
DOIs	https://doi.org/10.1016/j.bbrc.2014.07.054
Publication status	Published - 8 Aug 2014

Keywords

Inflammation
Luciferase assay
Promoter activity
Rat SAA

ASJC Scopus subject areas

Biophysics
Biochemistry
Molecular Biology
Cell Biology

Fields of Expertise

Human- & Biotechnology

Treatment code (Nähere Zuordnung)

Basic - Fundamental (Grundlagenforschung)
Experimental

Access to Document

10.1016/j.bbrc.2014.07.054Licence: CC BY-NC-ND 3.0

Cite this

Rossmann, C., Windpassinger, C., Brunner, D., Kovacevic, A., Schweighofer, N., Malli, R., Schuligoi, R., Prokesch, A., Kluve-Beckerman, B., Graier, W. F., Kratky, D., Sattler, W., & Malle, E. (2014). Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily. Biochemical and Biophysical Research Communications, 450(4), 1643-1649. https://doi.org/10.1016/j.bbrc.2014.07.054

Rossmann, C, Windpassinger, C, Brunner, D, Kovacevic, A, Schweighofer, N, Malli, R, Schuligoi, R, Prokesch, A, Kluve-Beckerman, B, Graier, WF , Kratky, D, Sattler, W & Malle, E 2014, 'Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily', Biochemical and Biophysical Research Communications, vol. 450, no. 4, pp. 1643-1649. https://doi.org/10.1016/j.bbrc.2014.07.054

@article{0eff51d8ce884b53b0fab7439c330785,

title = "Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily",

abstract = "The serum amyloid A (SAA) family of proteins is encoded by multiple genes, which display allelic variation and a high degree of homology in mammals. The SAA1/2 genes code for non-glycosylated acute-phase SAA1/2 proteins, that may increase up to 1000-fold during inflammation. The SAA4 gene, well characterized in humans (hSAA4) and mice (mSaa4) codes for a SAA4 protein that is glycosylated only in humans. We here report on a previously uncharacterized SAA4 gene (rSAA4) and its product in Rattus norvegicus, the only mammalian species known not to express acute-phase SAA. The exon/intron organization of rSAA4 is similar to that reported for hSAA4 and mSaa4. By performing 5′- and 3′RACE, we identified a 1830-bases containing rSAA4 mRNA (including a GA-dinucleotide tandem repeat). Highest rSAA4 mRNA expression was detected in rat liver. In McA-RH7777 rat hepatoma cells, rSAA4 transcription was significantly upregulated in response to LPS and IL-6 while IL-1α/β and TNFα were without effect. Luciferase assays with promoter-truncation constructs identified three proximal C/EBP-elements that mediate expression of rSAA4 in McA-RH7777 cells. In line with sequence prediction a 14-kDa non-glycosylated SAA4 protein is abundantly expressed in rat liver. Fluorescence microscopy revealed predominant localization of rSAA4-GFP-tagged fusion protein in the ER.",

keywords = "Inflammation, Luciferase assay, Promoter activity, Rat SAA",

author = "Christine Rossmann and Christian Windpassinger and Daniela Brunner and Alenka Kovacevic and Natascha Schweighofer and Roland Malli and Rufina Schuligoi and Andreas Prokesch and Barbara Kluve-Beckerman and Graier, {Wolfgang F.} and Dagmar Kratky and Wolfgang Sattler and Ernst Malle",

note = "Funding Information: Supported by the Austrian Science Fund (FWF-Austria) P19074 and SFB F3004 and F3007. ",

year = "2014",

month = aug,

day = "8",

doi = "10.1016/j.bbrc.2014.07.054",

language = "English",

volume = "450",

pages = "1643--1649",

journal = "Biochemical and Biophysical Research Communications",

issn = "1090-2104",

publisher = "Elsevier Inc.",

number = "4",

}

TY - JOUR

T1 - Characterization of rat serum amyloid A4 (SAA4)

T2 - A novel member of the SAA superfamily

AU - Rossmann, Christine

AU - Windpassinger, Christian

AU - Brunner, Daniela

AU - Kovacevic, Alenka

AU - Schweighofer, Natascha

AU - Malli, Roland

AU - Schuligoi, Rufina

AU - Prokesch, Andreas

AU - Kluve-Beckerman, Barbara

AU - Graier, Wolfgang F.

AU - Kratky, Dagmar

AU - Sattler, Wolfgang

AU - Malle, Ernst

N1 - Funding Information: Supported by the Austrian Science Fund (FWF-Austria) P19074 and SFB F3004 and F3007.

PY - 2014/8/8

Y1 - 2014/8/8

N2 - The serum amyloid A (SAA) family of proteins is encoded by multiple genes, which display allelic variation and a high degree of homology in mammals. The SAA1/2 genes code for non-glycosylated acute-phase SAA1/2 proteins, that may increase up to 1000-fold during inflammation. The SAA4 gene, well characterized in humans (hSAA4) and mice (mSaa4) codes for a SAA4 protein that is glycosylated only in humans. We here report on a previously uncharacterized SAA4 gene (rSAA4) and its product in Rattus norvegicus, the only mammalian species known not to express acute-phase SAA. The exon/intron organization of rSAA4 is similar to that reported for hSAA4 and mSaa4. By performing 5′- and 3′RACE, we identified a 1830-bases containing rSAA4 mRNA (including a GA-dinucleotide tandem repeat). Highest rSAA4 mRNA expression was detected in rat liver. In McA-RH7777 rat hepatoma cells, rSAA4 transcription was significantly upregulated in response to LPS and IL-6 while IL-1α/β and TNFα were without effect. Luciferase assays with promoter-truncation constructs identified three proximal C/EBP-elements that mediate expression of rSAA4 in McA-RH7777 cells. In line with sequence prediction a 14-kDa non-glycosylated SAA4 protein is abundantly expressed in rat liver. Fluorescence microscopy revealed predominant localization of rSAA4-GFP-tagged fusion protein in the ER.

AB - The serum amyloid A (SAA) family of proteins is encoded by multiple genes, which display allelic variation and a high degree of homology in mammals. The SAA1/2 genes code for non-glycosylated acute-phase SAA1/2 proteins, that may increase up to 1000-fold during inflammation. The SAA4 gene, well characterized in humans (hSAA4) and mice (mSaa4) codes for a SAA4 protein that is glycosylated only in humans. We here report on a previously uncharacterized SAA4 gene (rSAA4) and its product in Rattus norvegicus, the only mammalian species known not to express acute-phase SAA. The exon/intron organization of rSAA4 is similar to that reported for hSAA4 and mSaa4. By performing 5′- and 3′RACE, we identified a 1830-bases containing rSAA4 mRNA (including a GA-dinucleotide tandem repeat). Highest rSAA4 mRNA expression was detected in rat liver. In McA-RH7777 rat hepatoma cells, rSAA4 transcription was significantly upregulated in response to LPS and IL-6 while IL-1α/β and TNFα were without effect. Luciferase assays with promoter-truncation constructs identified three proximal C/EBP-elements that mediate expression of rSAA4 in McA-RH7777 cells. In line with sequence prediction a 14-kDa non-glycosylated SAA4 protein is abundantly expressed in rat liver. Fluorescence microscopy revealed predominant localization of rSAA4-GFP-tagged fusion protein in the ER.

KW - Inflammation

KW - Luciferase assay

KW - Promoter activity

KW - Rat SAA

UR - http://www.scopus.com/inward/record.url?scp=84906088661&partnerID=8YFLogxK

U2 - 10.1016/j.bbrc.2014.07.054

DO - 10.1016/j.bbrc.2014.07.054

M3 - Article

SN - 1090-2104

VL - 450

SP - 1643

EP - 1649

JO - Biochemical and Biophysical Research Communications

JF - Biochemical and Biophysical Research Communications

IS - 4

ER -

Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily

Abstract

Keywords

ASJC Scopus subject areas

Fields of Expertise

Treatment code (Nähere Zuordnung)

Access to Document

Other files and links

Fingerprint

FWF - APMAP in adipogenesis - The role of APMAP in adipogenesis and energy metabolism.

Cite this

Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily

Abstract

Keywords

ASJC Scopus subject areas

Fields of Expertise

Treatment code (Nähere Zuordnung)

Access to Document

Other files and links

Fingerprint

Projects

FWF - APMAP in adipogenesis - The role of APMAP in adipogenesis and energy metabolism.

Cite this