Literature DB >> 22444613

Genomics of metabolic adaptations in the peripartal cow.

J J Loor1.   

Abstract

The peripartal period is characterized by dramatic alterations in metabolism and function of key tissues such as liver, adipose and mammary. Metabolic regulation relies partly on transcriptional control of gene networks, a collection of DNA segments, which interact with a transcription factor or nuclear receptor, as a mechanism controlling the concentration of key enzymes in cells. These 'global' interactions can govern the rates at which genes in the network are transcribed into mRNA. The study of the entire genome, sub-networks or candidate genes at the mRNA level encompasses the broad field of genomics. Genomics of peripartal metabolic adaptations has traditionally been focused on candidate genes and more recently, using microarrays, on the broader transcriptome landscape. The candidate gene approach has expanded our knowledge on the functional adaptations of ureagenesis, fatty acid oxidation, gluconeogenesis, inflammation and growth hormone signaling in liver. More recent work with peripartal mammary tissue has used a gene network approach to study milk fat synthesis regulation as well as a candidate gene approach to study lipid transport, glucose uptake and inflammatory response. Network and pathway analysis of microarray data from cows fed different levels of dietary energy pre partum has revealed unique clusters encompassing functional categories including signal transduction, endoplasmic reticulum stress, peroxisome proliferator-activated receptors (PPARγ) signaling, PPARα signaling, immune or inflammatory processes and cell death in subcutaneous adipose tissue as well as liver. Of interest from a nutritional perspective is the potential to alter PPARγ signaling in adipose and PPARα signaling in liver as a means to enhance insulin sensitivity as well as fatty acid oxidation post partum. Major advances in understanding the metabolic adaptations of peripartal cows will come from using a systems biology approach to integrate data generated at the mRNA, protein, metabolite and tissue level across different nutritional management approaches and with cows of different genetic merit. This will allow the assembly of the important components needed to improve existing metabolic models of the peripartal cow and provide the tools to manipulate complex processes that could have significant long-term economic impact including lactation persistency, fertility and efficiency. An important goal of the future will be to apply additional experimental tools (e.g. gene silencing) and bioinformatics (e.g. transcription factor binding site identification) to studies focused on peripartal cows.

Entities:  

Year:  2010        PMID: 22444613     DOI: 10.1017/S1751731110000960

Source DB:  PubMed          Journal:  Animal        ISSN: 1751-7311            Impact factor:   3.240


  25 in total

1.  Different mitochondrial DNA copy number in liver and mammary gland of lactating cows with divergent genetic background for milk production.

Authors:  Rosemarie Weikard; Christa Kuehn
Journal:  Mol Biol Rep       Date:  2018-07-26       Impact factor: 2.316

Review 2.  Nutrigenomic Interventions to Address Metabolic Stress and Related Disorders in Transition Cows.

Authors:  Faiz-Ul Hassan; Asif Nadeem; Maryam Javed; Muhammad Saif-Ur-Rehman; Muhammad Aasif Shahzad; Jahanzaib Azhar; Borhan Shokrollahi
Journal:  Biomed Res Int       Date:  2022-06-11       Impact factor: 3.246

3.  Immunometabolism in livestock: triggers and physiological role of transcription regulators, nutrients, and microbiota.

Authors:  Juan J Loor; Ahmed A Elolimy
Journal:  Anim Front       Date:  2022-10-14

4.  Role of peroxisome proliferator-activated receptor-α on the synthesis of monounsaturated fatty acids in goat mammary epithelial cells.

Authors:  Huibin Tian; Jun Luo; Hengbo Shi; Xiaoying Chen; Jiao Wu; Yusheng Liang; Cong Li; Juan J Loor
Journal:  J Anim Sci       Date:  2020-03-01       Impact factor: 3.159

5.  How selected tissues of lactating holstein cows respond to dietary polyunsaturated fatty acid supplementation.

Authors:  Beate Hiller; Joaquin Angulo; Martha Olivera; Gerd Nuernberg; Karin Nuernberg
Journal:  Lipids       Date:  2012-11-06       Impact factor: 1.880

6.  RNA-seq analysis of differential gene expression in liver from lactating dairy cows divergent in negative energy balance.

Authors:  Matthew McCabe; Sinéad Waters; Dermot Morris; David Kenny; David Lynn; Chris Creevey
Journal:  BMC Genomics       Date:  2012-05-20       Impact factor: 3.969

7.  Dietary Lipid During Late-Pregnancy and Early-Lactation to Manipulate Metabolic and Inflammatory Gene Network Expression in Dairy Cattle Liver with a Focus on PPARs.

Authors:  Haji Akbar; Eduardo Schmitt; Michael A Ballou; Marcio N Corrêa; Edward J Depeters; Juan J Loor
Journal:  Gene Regul Syst Bio       Date:  2013-06-11

8.  Ruminant metabolic systems biology: reconstruction and integration of transcriptome dynamics underlying functional responses of tissues to nutrition and physiological state.

Authors:  Massimo Bionaz; Juan J Loor
Journal:  Gene Regul Syst Bio       Date:  2012-06-25

9.  Application of Top-Down and Bottom-up Systems Approaches in Ruminant Physiology and Metabolism.

Authors:  Khuram Shahzad; Juan J Loor
Journal:  Curr Genomics       Date:  2012-08       Impact factor: 2.236

10.  Regulation of Genes Involved in Carnitine Homeostasis by PPARα across Different Species (Rat, Mouse, Pig, Cattle, Chicken, and Human).

Authors:  Robert Ringseis; Gaiping Wen; Klaus Eder
Journal:  PPAR Res       Date:  2012-10-23       Impact factor: 4.964

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