Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • Resource and Technical Advances
    • Clinical Medicine
    • Reviews
    • Editorials
    • Perspectives
    • Top read articles
  • JCI This Month
    • Current issue
    • Past issues

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Concise Communication
  • Editorials
  • Viewpoint
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
ABT1 modifies SMARD1 pathology via interactions with IGHMBP2 and stimulation of ATPase and helicase activity
Gangadhar P. Vadla, … , Kamal Singh, Monique A. Lorson
Gangadhar P. Vadla, … , Kamal Singh, Monique A. Lorson
Published December 8, 2022
Citation Information: JCI Insight. 2023;8(2):e164608. https://doi.org/10.1172/jci.insight.164608.
View: Text | PDF
Research Article Genetics Neuroscience

ABT1 modifies SMARD1 pathology via interactions with IGHMBP2 and stimulation of ATPase and helicase activity

  • Text
  • PDF
Abstract

SMA with respiratory distress type 1 (SMARD1) and Charcot-Marie-Tooth type 2S (CMT2S) are results of mutations in immunoglobulin mu DNA binding protein 2 (IGHMBP2). IGHMBP2 is a UPF1-like helicase with proposed roles in several cellular processes, including translation. This study examines activator of basal transcription 1 (ABT1), a modifier of SMARD1-nmd disease pathology. Microscale thermophoresis and dynamic light scattering demonstrate that IGHMBP2 and ABT1 proteins directly interact with high affinity. The association of ABT1 with IGHMBP2 significantly increases the ATPase and helicase activity as well as the processivity of IGHMBP2. The IGHMBP2/ABT1 complex interacts with the 47S pre-rRNA 5′ external transcribed spacer and U3 small nucleolar RNA (snoRNA), suggesting that the IGHMBP2/ABT1 complex is important for pre-rRNA processing. Intracerebroventricular injection of scAAV9-Abt1 decreases FVB-Ighmbp2nmd/nmd disease pathology, significantly increases lifespan, and substantially decreases neuromuscular junction denervation. To our knowledge, ABT1 is the first disease-modifying gene identified for SMARD1. We provide a mechanism proposing that ABT1 decreases disease pathology in FVB-Ighmbp2nmd/nmd mutants by optimizing IGHMBP2 biochemical activity (ATPase and helicase activity). Our studies provide insight into SMARD1 pathogenesis, suggesting that ABT1 modifies IGHMBP2 activity as a means to regulate pre-rRNA processing.

Authors

Gangadhar P. Vadla, Sara M. Ricardez Hernandez, Jiude Mao, Mona O. Garro-Kacher, Zachary C. Lorson, Ronin P. Rice, Sarah A. Hansen, Christian L. Lorson, Kamal Singh, Monique A. Lorson

×

Figure 6

scAAV9-Abt1 delivery modifies the Ighmbp2nmd/nmd phenotype.

Options: View larger image (or click on image) Download as PowerPoint
scAAV9-Abt1 delivery modifies the Ighmbp2nmd/nmd phenotype.
(A) Illustra...
(A) Illustration of the self-complementary AAV9-Abt1 vector. The chicken β-actin promoter is used to express the Abt1 cDNA along with an optimized intron within the 5′ leader sequence and a synthetic poly A site. (B–E) WT (+/+), Ighmbp2nmd/nmd, and Ighmbp2nmd/nmd mice i.c.v. injected with scAAV9-Abt1 (1.5 × 1011 or 4 × 1011 viral genomes) are evaluated for lifespan (B), weight (C), time-to-right (P7–P26) (D), and hindlimb splay (P7–P26) (E). (F–H) Representative images of WT (+/+), Ighmbp2nmd/nmd, and Ighmbp2nmd/nmd mice injected with scAAV9-Abt1 (4 ×1011 viral genomes) at P7 (F), P12 (G), and P18 (H). Statistical analyses for lifespan and weight was 2-way ANOVA with Tukey’s multiple-comparison test; data are shown as mean ± SEM. Statistical analyses for TTR and HLS was ordinary 1-way ANOVA with Tukey’s multiple-comparison test.

Copyright © 2023 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts