Abstract

Problem statement: Mitochondrial transcription factor A (TFAM) is a nucleus-encoded protein that is a key activator of mitochondrial transcription as well as a major participant in mitochondrial genome replication. Genomic characterization of the porcine TFAM gene is, therefore, necessary to determine its involvement in regulation of fat depots and meat quality traits in pigs. Approach: Genomic DNA sequence was determined using a comparative in silico annotation approach. RT-PCR was used for analysis of alternative splicing. Genome location was determined using Radiation Hybrid (RH) mapping. Genetic marker was identified by sequencing and genotyped by the PCR-RFLP method with SacI. GENEPOP version 3.3 software was used for statistic analysis. Results: We determined both full-length cDNA and genomic DNA sequences of the porcine TFAM gene. Gene expression analysis revealed an alternative 5’ splice site, which excludes exon 4 of the pig gene. We assigned this gene to porcine chromosome 14 (SSC14). A G/A substitution was detected in intron 1 of porcine TFAM gene and genotyped on a total of 252 animals, including 165 from seven Chinese and 87 from five Western pig breeds. The Bayesian analysis via MCMC (Markov chain Monte Carlo) revealed that these two groups of pigs were well separated at this locus during the breed history; 95% of the posterior difference of TFAM allelic frequency between these two pig groups was greater than zero. Conclusion/Recommendations: All these data provided basic genomic information needed for further functional characterization of the porcine TFAM gene. Because marked differences in fat and lean tissue deposition exist between Western and Chinese pig breeds, the G557A mutation in the TFAM gene deserves further evaluation to determine its phenotypic effect on fattening and carcass traits in commercial pig populations.

Highlights

  • Mitochondrial transcription Factor A (TFAM; previously known as mtTFA) is an integral part of the basal mitochondrial transcription machinery in mammals[1]

  • In step 3, the genomic DNA was used as a template against the Expressed Sequence Tag (EST) databases for an electronic rapid amplification of cDNA ends (e-RACE) to generate a full-length cDNA sequence for the porcine gene

  • Such a process led to a comprehensive annotation of the porcine TFAM gene at both cDNA and genomic DNA levels

Read more

Summary

INTRODUCTION

Mitochondrial transcription Factor A (TFAM; previously known as mtTFA) is an integral part of the basal mitochondrial transcription machinery in mammals[1]. It is required for transcription of mammalian mitochondrial DNA (mtDNA) from the light-strand and heavy-strand promoters in the presence of mitochondrial transcription factors B1 (TFB1M), B2 (TFB2M) and mitochondrial RNA polymerase (POLRMT)[2]. Mice heterozygous for a targeted mutation of the Tfam gene exhibited reduced mtDNA copy number, while homozygous knockout embryos exhibited severe mtDNA loss and embryonic lethality, probably due to abolished transcription dependent priming of mtDNA replication[2,3].

MATERIALS AND METHODS
RESULTS
1: W and C
DISCUSSION
Findings
CONCLUSION
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call