44 DIFFERENTIAL REGULATION OF THE RAT LIVER SINUSOIDAL Na+-DEPENDENT BILE ACID TRANSPORTER GENE PROMOTER BY BILE ACIDS

Author(s):  
Saul Karpen ◽  
M. Ananthanarayanan ◽  
Frederick J. Suchy
2020 ◽  
Vol 158 (6) ◽  
pp. S-394-S-395
Author(s):  
Atsushi Nakajima ◽  
Sonoko Ishizaki ◽  
Shinsuke Kurosu ◽  
Shinya Taniguchi ◽  
Per-Göran Gillberg ◽  
...  

1998 ◽  
Vol 114 ◽  
pp. A1334
Author(s):  
P. Sauer ◽  
A. Stiehl ◽  
P. Kloeters-Plachky ◽  
BA Fitscher ◽  
HD Riedel ◽  
...  

2003 ◽  
Vol 124 (4) ◽  
pp. A104-A105
Author(s):  
Diana Jung ◽  
Amedeo C. Fantin ◽  
Ulrich Scheurer ◽  
Michael Fried ◽  
Gerd A. Kullak-Ublick

2008 ◽  
Vol 410 (2) ◽  
pp. 391-400 ◽  
Author(s):  
Antara Banerjee ◽  
Naissan Hussainzada ◽  
Akash Khandelwal ◽  
Peter W. Swaan

The hASBT (human apical Na+-dependent bile acid transporter) constitutes a key target of anti-hypercholesterolaemic therapies and pro-drug approaches; physiologically, hASBT actively reclaims bile acids along the terminal ileum via Na+ co-transport. Previously, TM (transmembrane segment) 7 was identified as part of the putative substrate permeation pathway using SCAM (substitute cysteine accessibility mutagenesis). In the present study, SCAM was extended through EL3 (extracellular loop 3; residues Arg254–Val286) that leads into TM7 from the exofacial matrix. Activity of most EL3 mutants was significantly hampered upon cysteine substitution, whereas ten (out of 31) were functionally inactive (<10% activity). Since only E282C lacked plasma membrane expression, EL3 amino acids predominantly fulfill critical functional roles during transport. Oppositely charged membrane-impermeant MTS (methanethiosulfonate) reagents {MTSET [(2-trimethylammonium) ethyl MTS] and MTSES [(2-sulfonatoethyl) MTS]} produced mostly similar inhibition profiles wherein only middle and descending loop segments (residues Thr267–Val286) displayed significant MTS sensitivity. The presence of bile acid substrate significantly reduced the rates of MTS modification for all MTS-sensitive mutants, suggesting a functional association between EL3 residues and bile acids. Activity assessments at equilibrative [Na+] revealed numerous Na+-sensitive residues, possibly performing auxiliary functions during transport such as transduction of protein conformational changes during translocation. Integration of these data suggests ligand interaction points along EL3 via electrostatic interactions with Arg256, Glu261 and probably Glu282 and a potential cation-π interaction with Phe278. We conclude that EL3 amino acids are essential for hASBT activity, probably as primary substrate interaction points using long-range electrostatic attractive forces.


2000 ◽  
Vol 66 (3) ◽  
pp. 1107-1113 ◽  
Author(s):  
James E. Wells ◽  
Phillip B. Hylemon

ABSTRACT Clostridium sp. strain TO-931 can rapidly convert the primary bile acid cholic acid to a potentially toxic compound, deoxycholic acid. Mixed oligonucleotide probes were used to isolate a gene fragment encoding a putative bile acid transporter fromClostridium sp. strain TO-931. This DNA fragment had 60% nucleotide sequence identity to a known bile acid transporter gene fromEubacterium sp. strain VPI 12708, another bile acid-7α-dehydroxylating intestinal bacterium. The DNA (9.15 kb) surrounding the transporter gene was cloned fromClostridium sp. strain TO-931 and sequenced. Within this larger DNA fragment was a 7.9-kb region, containing six successive open reading frames (ORFs), that was encoded by a single 8.1-kb transcript, as determined by Northern blot analysis. The gene arrangement and DNA sequence of the Clostridium sp. strain TO-931 operon are similar to those of a Eubacterium sp. strain VPI 12708 bile acid-inducible operon containing nine ORFs. Several genes in theEubacterium sp. strain VPI 12708 operon have been shown to encode products required for bile acid 7α-dehydroxylation. InClostridium sp. strain TO-931, genes potentially encoding bile acid-coenzyme A (CoA) ligase, 3α-hydroxysteroid dehydrogenase, bile acid 7α-dehydratase, bile acid-CoA hydrolase, and a bile acid transporter were similar in size and exhibited amino acid homology to similar gene products from Eubacterium sp. strain VPI 12708 (encoded by baiB, baiA, baiE,baiF, and baiG, respectively). However, no genes similar to Eubacterium sp. strain VPI 12708biaH or baiI were found in theClostridium sp. strain TO-931 bai operon, and the two putative Eubacterium sp. strain VPI 12708 genes,baiC and baiD, were arranged in one continuous ORF in Clostridium sp. strain TO-931. Intergene regions showed no significant DNA sequence similarity, but primer extension analysis identified a region 115 bp upstream from the first ORF that exhibited 58% identity to a bai operator/promoter region identified in Eubacterium sp. strain VPI 12708. These results indicate that the gene organization, gene product amino acid sequences, and promoters of the bile acid-inducible operons ofClostridium sp. strain TO-931 and Eubacteriumsp. strain VPI 12708 are highly conserved.


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