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牛乳腺脂肪合成关键酶基因在乳汁体细胞中的表达研究

谢佳喜 朱河水 杨国宇 李宏基 郭豫杰 汪新建 王月影

畜牧兽医学报2011,Vol.42Issue(8):1081-1087,7.
畜牧兽医学报2011,Vol.42Issue(8):1081-1087,7.

牛乳腺脂肪合成关键酶基因在乳汁体细胞中的表达研究

The Expression of the Related Fatty Acid Synthesis Key Enzyme Genes in Bovine Somatic Cell

谢佳喜 1朱河水 1杨国宇 1李宏基 1郭豫杰 1汪新建 1王月影1

作者信息

  • 1. 河南农业大学农业部动物生长发育调控重点开放实验室,郑州450002
  • 折叠

摘要

Abstract

To clarify the molecular mechanism of milk fat synthesis, optimizing ruminant raw milk, particularly providing theory basis for nutrition regulation and heredity improving for milk fat. Somatic cells in colostrum milk, mature milk and involution milk were selected and housekeeping gene GAPDH was selected as reference, the semi-quantitive RT-PCR was used to analyze the expression of LPL, CD36, VLDLR, ACSS2, ACSLl, FABP3, ACC, FASN, SCD, AD-FP, XDH and BTN1A1 mRNA in milk. The results showed that the genes LPL, CD36, VLDLR, ACSS2, ACSLl, FABP3, ACC, FASN, SCD, ADFP, XDH and BTNV1A1 mRNA expressed in the colostrum milk, mature milk and involution milk. However the genes ACC and FASN were not detected in mature milk and involution milk. The relative quantitive results showed that the expression level of LPL, CD36, VLDLR, ACSS2, ACSLl, FABP3, ACC, FASN, SCD, ADFP, XDH and BTN1A1 mRNA in mature milk and involution milk were significantly decreased(P<0. 05) , compared with colostrum milk. The transcription level difference of these genes was not significant(P>0. 05) between mature milk and involution milk. These re-suits suggest that the ability of milk fat synthesis in colostrum is higher than that in mature milk and involution milk, and the expression of fatty acid synthetic key genes is related to fat transpor-tant and metabolism of cell.

关键词

乳汁/体细胞/脂肪合成关键酶基因/RT-PCR

Key words

milk/ somatic cell/ fatty acid synthetic key enzyme genes/ RT-PCR

分类

农业科技

引用本文复制引用

谢佳喜,朱河水,杨国宇,李宏基,郭豫杰,汪新建,王月影..牛乳腺脂肪合成关键酶基因在乳汁体细胞中的表达研究[J].畜牧兽医学报,2011,42(8):1081-1087,7.

基金项目

“十一五”国家科技攻关计划子课题(2006BAD04A03-10) (2006BAD04A03-10)

河南省科技攻关课题(072102140002) (072102140002)

畜牧兽医学报

OA北大核心CSCDCSTPCD

0366-6964

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