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1.
J Anim Physiol Anim Nutr (Berl) ; 100(3): 422-30, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26613803

ABSTRACT

Milk protein synthesis in the mammary gland involves expression of six major milk proteins' genes whose nutritional regulation remains poorly defined. In this study, the effect of long-term under- and overfeeding on the expression of as1-casein: CSN1S1, as2-casein: CSN1S2, ß-casein: CSN2, κ-casein: CSN3, α-lactalbumin: LALBA and ß-lactoglobulin: BLG gene in goat mammary tissue (MT) was examined. Twenty-four lactating dairy goat, at 90-98 days in milk, were divided into three homogenous subgroups and fed the same ration, for 60 days, in quantities which met 70% (underfeeding), 100% (control) and 130% (overfeeding) of their energy and crude protein requirements. The results showed a significant decrease in mRNA of CSN1S2, CSN2, CSN3 and LALBA genes in the MT of underfed goats compared with the overfed and on the CSN1S1 and BLG gene expressions in the MT of underfed goats compared with the respective control and overfed. CSN2 was the most abundant transcript in goat MT relative to the other milk proteins' genes. Significantly positive correlations were observed between the mRNA levels of caseins' and BLG genes with the milk yield. Moreover, a significant correlation was found between the mRNA levels of CSN1S2 with the milk protein, lactose content and lactose yield and also between the LALBA gene expression with the lactose content and lactose yield respectively. In conclusion, the feeding level and consequently the nutrients availability affected the milk lactose content, protein and lactose yield as well as the milk volume by altering the CSN1S1, CSN1S2, CSN2, CSN3, LALBA and BLG gene expression involved in their metabolic pathways.


Subject(s)
Animal Feed/analysis , Diet/veterinary , Energy Intake , Gene Expression Regulation/drug effects , Goats/physiology , Milk Proteins/metabolism , Animals , Female , Mammary Glands, Animal/metabolism , Milk/chemistry , Milk Proteins/genetics , Nutritional Requirements , Time Factors
2.
Planta ; 228(1): 37-49, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18320213

ABSTRACT

The biosynthesis of the polyamines spermidine (Spd) and spermine (Spm) from putrescine (Put) is catalysed by the consequent action of two aminopropyltransferases, spermidine synthase (SPDS EC: 2.5.1.16) and spermine synthase (SPMS EC: 2.5.1.22). Two cDNA clones coding for SPDS and SPMS homologues in the nitrogen-fixing nodules of the model legume Lotus japonicus were identified. Functionality of the encoded polypeptides was confirmed by their ability to complement spermidine and spermine deficiencies in yeast. The temporal and spatial expression pattern of the respective genes was correlated with the accumulation of total polyamines in symbiotic and non-symbiotic organs. Expression of both genes was maximal at early stages of nodule development, while at later stages the levels of both transcripts declined. Both genes were expressed in nodule inner cortical cells, vascular bundles, and central tissue. In contrast to gene expression, increasing amounts of Put, Spd, and Spm were found to accumulate during nodule development and after maturity. Interestingly, nodulated plants exhibited systemic changes in both LjSPDS and LjSPMS transcript levels and polyamine content in roots, stem and leaves, in comparison to uninoculated plants. These results give new insights into the neglected role of polyamines during nodule development and symbiotic nitrogen fixation (SNF).


Subject(s)
Lotus/genetics , Plant Proteins/genetics , Spermidine Synthase/genetics , Spermine Synthase/genetics , Amino Acid Sequence , Genetic Complementation Test , In Situ Hybridization , Lotus/enzymology , Lotus/metabolism , Molecular Sequence Data , Plant Proteins/metabolism , Polyamines/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Root Nodules, Plant/enzymology , Root Nodules, Plant/genetics , Root Nodules, Plant/metabolism , Sequence Homology, Amino Acid , Spermidine Synthase/metabolism , Spermine Synthase/metabolism , Transcription, Genetic
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