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Developmental changes in physiological amino acids and hepatic methionine remethylation enzyme activities in E10‐21 chick embryos and D1‐49 broilers
Author(s) -
Lu Jianwei,
Weil Jordan,
Cerrate Sandro,
Coon Craig
Publication year - 2020
Publication title -
journal of animal physiology and animal nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.651
H-Index - 56
eISSN - 1439-0396
pISSN - 0931-2439
DOI - 10.1111/jpn.13390
Subject(s) - putrescine , methionine , serine hydroxymethyltransferase , embryo , spermidine , biology , medicine , glycine , spermine , endocrinology , polyamine , homocysteine , methyltransferase , biochemistry , transmethylation , serine , embryogenesis , enzyme , amino acid , methylation , microbiology and biotechnology , gene
The remethylation of homocysteine to methionine is important for chick embryos to sustain the S‐adenosylmethionine transmethylation reactions, which are essential for the rapid proliferation of cells. Developmental changes in hepatic 5‐methyltetrahydrofolate‐homocysteine methyltransferase (MFMT), betaine‐homocysteine methyltransferase (BHMT) and hepatic serine hydroxymethyltransferase (SHMT) were determined in E10‐21 Cobb 500 broiler chick embryos and hatched chicks from D1‐49. Hepatic levels of free serine, glycine, putrescine, spermidine and spermine levels were also determined. Analyses showed hepatic MFMT‐specific activity doubled from E10 to E12, with remaining embryo development experiencing small fluctuations in activity through E21. Hepatic MFMT doubled immediately after hatch, with peak activity occurring at D3. Afterwards, hepatic MFMT‐specific activity steadily declined from D7‐49. Hepatic BHMT activity was higher from E10 to E16 of embryogenesis, decreased rapidly at E17 and remained lower through E21 ( p < .05). Hepatic BHMT‐specific activity was also lower in chicks, with the exception of a peak in specific activity on D7. BHMT activity returned to lower levels by D21. Throughout embryogenesis, hepatic SHMT activity in chick embryos remained relatively constant except for a decrease at 13E, followed by an increase at 14E. Maximal activity of SHMT was found the first day post‐hatch. Additionally, SHMT activity was significantly lower in growing chicks than that in embryos. Hepatic‐free serine and glycine levels were negatively correlated with SHMT in hatched chicks. Hepatic polyamine, putrescine and spermidine shared a similar development pattern: peak level in the middle of incubation, low at late embryogenesis and lowest during the post‐hatch period except an increase within one week after hatch. The sharp increase in hepatic concentrations of glycine, serine and putrescine, along with increased specific activities of MHMT, BHMT and SHMT from D1‐7, suggests that methionine conservation (remethylation from homocysteine) and glycine/serine is critical for young chicks for organ growth, maturation, and development.