Abstract

At the central region of the mammalian major histocompatibility complex (MHC) is a complement gene cluster that codes for constituents of complement C3 convertases (C2, factor B and C4). Complement activation drives the humoral effector functions for immune response. Sandwiched between the genes for serine proteinase factor B and anchor protein C4 are four less known but critically important genes coding for essential functions related to metabolism and surveillance of RNA during the transcriptional and translational processes of gene expression. These four genes are NELF-E (RD), SKIV2L (SKI2W), DXO (DOM3Z) and STK19 (RP1 or G11) and dubbed as NSDK. NELF-E is the subunit E of negative elongation factor responsible for promoter proximal pause of transcription. SKIV2L is the RNA helicase for cytoplasmic exosomes responsible for degradation of de-polyadenylated mRNA and viral RNA. DXO is a powerful enzyme with pyro-phosphohydrolase activity towards 5′ triphosphorylated RNA, decapping and exoribonuclease activities of faulty nuclear RNA molecules. STK19 is a nuclear kinase that phosphorylates RNA-binding proteins during transcription. STK19 is also involved in DNA repair during active transcription and in nuclear signal transduction. The genetic, biochemical and functional properties for NSDK in the MHC largely stay as a secret for many immunologists. Here we briefly review the roles of (a) NELF-E on transcriptional pausing; (b) SKIV2L on turnover of deadenylated or expired RNA 3′→5′ through the Ski-exosome complex, and modulation of inflammatory response initiated by retinoic acid-inducible gene 1-like receptor (RLR) sensing of viral infections; (c) DXO on quality control of RNA integrity through recognition of 5′ caps and destruction of faulty adducts in 5′→3′ fashion; and (d) STK19 on nuclear protein phosphorylations. There is compelling evidence that a dysregulation or a deficiency of a NSDK gene would cause a malignant, immunologic or digestive disease.

Highlights

  • In 1984, Professor Rodney Porter’s team in Oxford reported the cloning and confirmed the physical linkage of the genes for human complement C4A and C4B, factor B and C2 through overlapping cosmids [1]

  • We briefly review the roles of (a) Negative Elongation Factor Subunit E (NELF-E) on transcriptional pausing; (b) SKIV2L on turnover of deadenylated or expired RNA 30 →50 through the Ski-exosome complex, and modulation of inflammatory response initiated by retinoic acid-inducible gene 1-like receptor (RLR) sensing of viral infections; (c) DXO on quality control of RNA integrity through recognition of 50 caps and destruction of faulty adducts in 50 →30 fashion; and (d) STK19 on nuclear protein phosphorylations

  • It appears that 60% of the trichohepatoenteric syndrome (THES) patients had a genetic deficiency of TTC37 [59] and 40% had a deficiency of SKIV2L [78], and many of those homozygous deficiencies were the results of consanguineous marriage

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Summary

Introduction

In 1984, Professor Rodney Porter’s team in Oxford reported the cloning and confirmed the physical linkage of the genes for human complement C4A and C4B, factor B and C2 through overlapping cosmids [1]. The complement system is a major effector arm for both innate and adaptive immune bit puzzling that the genes for C4 and factor B are separated by a large gap of 30 kb. The conserved coding sequences between human and mouse genes are highlighted in purple. Locations of CpG rich dinucleotides are shown as human and mouse genes are highlighted in purple. RNA quality control, decapping and 50 →30 RNA decay https://www.ncbi.nlm.nih.gov/gene/1797

NELF-E or RD
A Gene within a Gene: miR-1236 in Intron 3 of NELF-E
SKIV2L or SKI2W
DXO or DOM3Z
Findings
Conclusions
Full Text
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