Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome

Circ Res. 2022 Jan 7;130(1):80-95. doi: 10.1161/CIRCRESAHA.120.318141. Epub 2021 Nov 23.

Abstract

Background: The LDLR (low-density lipoprotein receptor) in the liver is the major determinant of LDL-cholesterol levels in human plasma. The discovery of genes that regulate the activity of LDLR helps to identify pathomechanisms of hypercholesterolemia and novel therapeutic targets against atherosclerotic cardiovascular disease.

Methods: We performed a genome-wide RNA interference screen for genes limiting the uptake of fluorescent LDL into Huh-7 hepatocarcinoma cells. Top hit genes were validated by in vitro experiments as well as analyses of data sets on gene expression and variants in human populations.

Results: The knockdown of 54 genes significantly inhibited LDL uptake. Fifteen of them encode for components or interactors of the U2-spliceosome. Knocking down any one of 11 out of 15 genes resulted in the selective retention of intron 3 of LDLR. The translated LDLR fragment lacks 88% of the full length LDLR and is detectable neither in nontransfected cells nor in human plasma. The hepatic expression of the intron 3 retention transcript is increased in nonalcoholic fatty liver disease as well as after bariatric surgery. Its expression in blood cells correlates with LDL-cholesterol and age. Single nucleotide polymorphisms and 3 rare variants of one spliceosome gene, RBM25, are associated with LDL-cholesterol in the population and familial hypercholesterolemia, respectively. Compared with overexpression of wild-type RBM25, overexpression of the 3 rare RBM25 mutants in Huh-7 cells led to lower LDL uptake.

Conclusions: We identified a novel mechanism of posttranscriptional regulation of LDLR activity in humans and associations of genetic variants of RBM25 with LDL-cholesterol levels.

Keywords: cardiovascular diseases; endocytosis; hepatocytes; hypercholesterolemia; spliceosomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cholesterol / metabolism
  • HEK293 Cells
  • Hep G2 Cells
  • Humans
  • Lipoproteins, LDL / metabolism
  • Liver / metabolism
  • Mutation
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • RNA Splicing*
  • Receptors, LDL / genetics*
  • Receptors, LDL / metabolism
  • Spliceosomes / metabolism

Substances

  • LUC7L3 protein, human
  • Lipoproteins, LDL
  • Nuclear Proteins
  • Receptors, LDL
  • Cholesterol