Literature DB >> 1657504

Betaine-homocysteine methyltransferase: organ distribution in man, pig and rat and subcellular distribution in the rat.

M P McKeever1, D G Weir, A Molloy, J M Scott.   

Abstract

1. Conflicting reports exist as to the organ distribution of betaine-homocysteine methyltransferase (EC 2.1.1.5). It is important to establish its presence or absence in brain, since its substrate, betaine, has recently become established in the treatment of certain diseases involving this organ. 2. It remains unclear whether the reported success of this treatment results from the use of betaine to methylate homocysteine and produce methionine in situ in neural tissue, or whether the effect is secondary to these same reductions happening in other organs, such as the liver. The former would require the presence of betaine-homocysteine methyltransferase in neural tissue. 3. This study demonstrates the complete absence of any activity for this enzyme in the brain of the three species examined. The enzyme was found to be present in both the liver and kidney of man and pig, but only in the liver of the rat. 4. The only source of betaine in cells is via the oxidation of choline. Since the enzymes involved in this conversion have never been shown to exist anywhere other than the mitochondria, it has been assumed that the methyltransferase is also mitochondrial. In this study, it is demonstrated that the enzyme exists only in the cytoplasm of rat liver cells.

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Year:  1991        PMID: 1657504     DOI: 10.1042/cs0810551

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  34 in total

1.  Tissue specificity of rat mitochondrial dimethylglycine dehydrogenase expression.

Authors:  H Lang; K Minaian; N Freudenberg; R Hoffmann; R Brandsch
Journal:  Biochem J       Date:  1994-04-15       Impact factor: 3.857

2.  Effect of regular exercise on homocysteine concentrations: the HERITAGE Family Study.

Authors:  Tomohiro Okura; Tuomo Rankinen; Jacques Gagnon; Suzanne Lussier-Cacan; Jean Davignon; Arthur S Leon; D C Rao; James S Skinner; Jack H Wilmore; Claude Bouchard
Journal:  Eur J Appl Physiol       Date:  2006-09-19       Impact factor: 3.078

3.  Autophagic activity measured in whole rat hepatocytes as the accumulation of a novel BHMT fragment (p10), generated in amphisomes by the asparaginyl proteinase, legumain.

Authors:  Anders Øverbye; Frank Sætre; Linda Korseberg Hagen; Harald Thidemann Johansen; Per O Seglen
Journal:  Autophagy       Date:  2011-09-01       Impact factor: 16.016

4.  Influence of vitamin B12 on brain methionine adenosyltransferase activity in senile dementia of the Alzheimer's type.

Authors:  C Gomes-Trolin; C G Gottfries; B Regland; L Oreland
Journal:  J Neural Transm (Vienna)       Date:  1996       Impact factor: 3.575

5.  Ad libitum choline intake in healthy individuals meets or exceeds the proposed adequate intake level.

Authors:  Leslie M Fischer; Julie A Scearce; Mei-Heng Mar; Jayanti R Patel; Renee T Blanchard; Beth A Macintosh; Marjorie G Busby; Steven H Zeisel
Journal:  J Nutr       Date:  2005-04       Impact factor: 4.798

6.  Ethanol lowers glutathione in rat liver and brain and inhibits methionine synthase in a cobalamin-dependent manner.

Authors:  Mostafa I Waly; Kusum K Kharbanda; Richard C Deth
Journal:  Alcohol Clin Exp Res       Date:  2010-12-01       Impact factor: 3.455

7.  S-alkylated homocysteine derivatives: new inhibitors of human betaine-homocysteine S-methyltransferase.

Authors:  Jiri Jiracek; Michaela Collinsova; Ivan Rosenberg; Milos Budesinsky; Eva Protivinska; Hana Netusilova; Timothy A Garrow
Journal:  J Med Chem       Date:  2006-06-29       Impact factor: 7.446

8.  Persistent hypermethioninaemia with dominant inheritance.

Authors:  H J Blom; A J Davidson; J D Finkelstein; A S Luder; I Bernardini; J J Martin; A Tangerman; J M Trijbels; S H Mudd; S I Goodman
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

9.  Suppression of the protein tyrosine phosphatase receptor type O gene (PTPRO) by methylation in hepatocellular carcinomas.

Authors:  Tasneem Motiwala; Kalpana Ghoshal; Anindita Das; Sarmila Majumder; Dieter Weichenhan; Yue-Zhong Wu; Kristen Holman; S Jill James; Samson T Jacob; Christoph Plass
Journal:  Oncogene       Date:  2003-09-25       Impact factor: 9.867

Review 10.  The Pediatric Methionine Requirement Should Incorporate Remethylation Potential and Transmethylation Demands.

Authors:  Jason L Robinson; Robert F Bertolo
Journal:  Adv Nutr       Date:  2016-05-16       Impact factor: 8.701

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