There are gaps in what is known about the metabolism of some mammalian small RNA species. Our present observations can be summarized as follows. The level of radiolabeled mature U1 KNA doubled between 2 and 24 hr of label chase, while that of all other small RNA species tested did not change. These
Cobalamin metabolism in cultured human chorionic villus cells
β Scribed by James A. Begley; Pamela D. Colligan; Richard C. Chu; Charles A. Hall
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 572 KB
- Volume
- 156
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Cobalamin (Cbl, vitamin B,J metabolism was analyzed in cultures of human chorionic villus (CV) cells obtained at 9-10 weeks of gestation. CV cells were shown to synthesize transcobalamin II (TCII) and to possess a high affinity receptor for that molecule. The cells bound and internalized radioactive cyanocobalamin (CN[57Co]Cbl) cornplexed to TCII. This internalized CN['7Co]Cbl was found to be converted to both methylCbl and adenosylcbl, the two intracellular coenzyme forms of Cbl, and bound to the two known intracellular Cbl requiring enzymes, methionine synthase (MS) and methylmalonyl-CoA mutase. Both enzyme systems were found to be functional in the intact cell by demonstrating the incorporation of the radioactive label from both I ''C]CH,-tetrahydrofolate and ('4C]propionate into acid insoluble products. MS activity was also detected in lysed cell material. CV cells were shown not to be auxotrophic for methionine since they were able to utilize homocysteine in place of methionine for cell division. Since CV cells are capable of performing many of the complex events associated with Cbl metabolism, it may be possible to use these cells to diagnose genetic defects of Cbl metabolism.
o 1993 ~i l e y -~i s s ,
Inc
Vitamin B,, (Cbl, cobalamin) acts as a precursor to cofactors for methylmalonyl-CoA mutase (MM-CoA mutase) and methionine synthase (MS). Defects in pro-
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