Abstract

BackgroundZinc (Zn) is an essential trace element. However, Zn bioavailability from commonly consumed plants may be reduced due to phytic acid. Zn supplementation has been used to treat diarrheal disease in children, and in the U.S. swine industry at pharmacological levels to promote growth and fecal consistency, but underlying mechanisms explaining these beneficial effects remain unknown. Moreover, adding supplemental phytase improves Zn bioavailability. Thus, we hypothesized that benefits of pharmacological Zn supplementation result from changes in gene expression that could be further affected by supplemental phytase. The goal of this study was to investigate the effects of feeding newly weaned pigs dietary Zn (150, 1,000, or 2,000 mg Zn/kg) as Zn oxide with or without phytase [500 phytase units (FTU)/kg] for 14 d on hepatic gene expression. Liver RNA from pigs fed 150, 1,000, or 2,000 mg Zn/kg, or 1,000 mg Zn/kg with phytase (n = 4 per treatment) was reverse transcribed and examined using the differential display reverse transcription polymerase chain reaction technique. Liver RNA from pigs fed 150 or 2,000 mg Zn/kg (n = 4 per treatment) was also evaluated using a 70-mer oligonucleotide microarray.ResultsExpressed sequence tags for 61 putatively differentially expressed transcripts were cloned and sequenced. In addition, interrogation of a 13,297 element oligonucleotide microarray revealed 650 annotated transcripts (FDR ≤ 0.05) affected by pharmacological Zn supplementation. Seven transcripts exhibiting differential expression in pigs fed pharmacological Zn with sequence similarities to genes encoding GLO1, PRDX4, ACY1, ORM1, CPB2, GSTM4, and HSP70.2 were selected for confirmation. Relative hepatic GLO1 (P < 0.0007), PRDX4 (P < 0.009) and ACY1 (P < 0.01) mRNA abundances were confirmed to be greater in pigs fed 1,000 (n = 8) and 2,000 (n = 8) mg Zn/kg than in pigs fed 150 (n = 7) mg Zn/kg. Relative hepatic HSP70.2 (P < 0.002) mRNA abundance was confirmed to be lower in pigs fed 2,000 mg Zn/kg than in pigs fed 150 or 1,000 mg Zn/kg.ConclusionResults suggest that feeding pharmacological Zn (1,000 or 2,000 mg Zn/kg) affects genes involved in reducing oxidative stress and in amino acid metabolism, which are essential for cell detoxification and proper cell function.

Highlights

  • Zinc (Zn) is an essential trace element

  • In this paper we report 61 amplicons identified by differential display reverse transcription polymerase chain reaction (DDRTPCR) and 650 annotated genes (FDR ≤ 0.05) identified by microarray analysis with putative differential gene expression, of which 5 transcripts with roles in oxidative stress reduction and amino acid metabolism were confirmed to have differential expression in pigs fed pharmacological Zn diets

  • Identification of differentially expressed genes by oligonucleotide microarray analysis To further monitor gene expression changes due to pharmacological Zn supplementation, we conducted a transcriptional profiling analysis using a commercially available pig 70-mer oligonucleotide set spotted on glass slide microarrays

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Summary

Introduction

Zinc (Zn) is an essential trace element. Zn bioavailability from commonly consumed plants may be reduced due to phytic acid. Liver RNA from pigs fed 150, 1,000, or 2,000 mg Zn/kg, or 1,000 mg Zn/kg with phytase (n = 4 per treatment) was reverse transcribed and examined using the differential display reverse transcription polymerase chain reaction technique. The trace mineral zinc (Zn) is involved in gene expression in numerous ways including DNA replication, RNA transcription, through the activity of transcription factors, DNA and RNA polymerases, signal transduction, oxidative stress and playing a role in programmed cell death [3]. It was recently estimated that almost 3,000 different proteins encoded by the human genome bind zinc [4]. An example of such proteins is metallothionein (MT), which exerts a protective effect against stress by acting as an antioxidant, and as a Zn storage and transfer protein [5]. The transcriptional regulation of the MT gene by dietary Zn has been demonstrated in rats [6]

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