Markovac J, Erickson R P
Biochem Pharmacol. 1985 Oct 1;34(19):3421-5. doi: 10.1016/0006-2952(85)90712-9.
The effects of the mouse major histocompatibility complex, H-2, on phospholipid methyltransferase I and II activities were investigated on hepatocyte membranes from inbred, congenic and recombinant strains. Each methyltransferase was assayed individually by measuring the incorporation of radiolabel from S-adenosyl-L-[methyl-3H]methionine into endogenous phospholipids. Our results indicate that H-2 exerted a significant effect on methyltransferase I but not on methyltransferase II activity. Thus, as in lower eukaryotes, two distinct enzymes were involved in methylation of phosphatidylethanolamine (PE) to phosphatidylcholine (PC). In addition, this effect was localized to the K end of the major histocompatibility complex by the use of recombinant haplotypes.
研究了小鼠主要组织相容性复合体H-2对近交系、同源近交系和重组品系肝细胞膜上磷脂甲基转移酶I和II活性的影响。通过测量放射性标记物从S-腺苷-L-[甲基-³H]甲硫氨酸掺入内源性磷脂中的量,分别对每种甲基转移酶进行测定。我们的结果表明,H-2对甲基转移酶I有显著影响,但对甲基转移酶II活性没有影响。因此,与低等真核生物一样,两种不同的酶参与了磷脂酰乙醇胺(PE)向磷脂酰胆碱(PC)的甲基化过程。此外,通过使用重组单倍型,这种影响定位于主要组织相容性复合体的K端。