Reference genes for gene expression profiling in mouse models of Listeria monocytogenes infection

Author:

Tavares Lethicia Souza1,Oliveira-Silva Roberta Lane2ORCID,Moura Marcelo Tigre3ORCID,da Silva Jéssica Barboza2,Benko-Iseppon Ana Maria2ORCID,Lima-Filho José Vitor1

Affiliation:

1. Departamento de Biologia, Universidade Federal Rural de Pernambuco, Recife, PE, Brasil

2. Departamento de Genética, Universidade Federal de Pernambuco, Recife, PE, Brasil

3. Departamento de Biologia Celular e Molecular, Centro de Biotecnologia, Campus I, Universidade Federal da Paraíba, João Pessoa, PB, Brasil

Abstract

RT-qPCR dissects transcription-based processes but requires reference genes (RGs) for data normalization. This study prospected RGs for mouse macrophages (pMØ) and spleen infected with Listeria monocytogenes. The pMØ were infected in vitro with L. monocytogenes or vehicle for 4 h. Mice were injected with L. monocytogenes (or vehicle) and euthanized 24 h post-injection. The RGs came from a multispecies primer set, from the literature or designed here. The RG ranking relied on GeNorm, NormFinder, BestKeeper, Delta-CT and RefFinder. B2m- H3f3a- Ppia were the most stable RGs for pMØ, albeit RG indexes fine-tuned estimations of cytokine relative expression. Actβ-Ubc- Ppia were the best RGs for spleen but modestly impacted the cytokine relative expression. Hence, mouse models of L. monocytogenes require context-specific RGs for RT-qPCR, thus reinforcing its paramount contribution to accurate gene expression profiling.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Future Science Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Biotechnology

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