Hoi1 targets the yeast BLTP2 protein to ER-PM contact sites to regulate lipid homeostasis
Data files
Apr 23, 2025 version files 4.42 KB
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Dziurdzik_Hoi1_Data.zip
1.52 KB
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README.md
2.89 KB
Abstract
Membrane contact sites between organelles are important for maintaining cellular lipid homeostasis. Members of the recently identified family of bridge-like lipid transfer proteins (BLTPs) span opposing membranes at these contact sites to enable the rapid transfer of bulk lipids between organelles. While the VPS13 and ATG2 family members use organelle-specific adaptors for membrane targeting, the mechanisms that regulate other bridge-like transporters remain unknown. Here, we identify the conserved protein Ybl086c, which we name Hoi1 (Hob interactor 1), as an adaptor that targets the yeast BLTP2-like proteins Fmp27/Hob1 and Hob2 to ER-PM contact sites. Two separate Hoi1 domains interface with alpha-helical projections that decorate the central hydrophobic channel on Fmp27, and loss of these interactions disrupts cellular sterol homeostasis. The mutant phenotypes of BLTP2 and HOI1 orthologs indicate these proteins act in a shared pathway in worms and flies. Together, this suggests that Hoi1-mediated recruitment of BLTP2-like proteins represents an evolutionarily conserved mechanism for regulating lipid transport at membrane contact sites.
Dataset DOI: 10.5061/dryad.wdbrv160w
Description of the data and file structure
This file contains the raw data used to generate the figures produced by the Bashirullah Lab in the preprint: Dziurdzik SK, Sridhar V, Eng H, Neuman SD, Yan J, Davey M, Taubert S, Bashirullah A, Conibear E. Hoi1 targets the yeast BLTP2 protein to ER-PM contact sites to regulate lipid homeostasis. bioRxiv [Preprint]. 2025 Feb 19:2025.02.11.637747. doi: 10.1101/2025.02.11.637747. PMID: 39990326; PMCID: PMC11844476. This manuscript characterizes the function of a novel adapter protein that regulates localization of the bridge-like lipid transfer protein (BLTP) BLTP2 to endoplasmic reticulum-plasma membrane (ER-PM) contact sites. This dataset includes quantitative reverse transcription PCR (qRT-PCR) data and body size/pupa volume data.
Each file name contains a reference to the figure where the data is published, as well as a description of the type of data included in the file.
Files and variables
Figure7FqRTPCRData.csv
This file contains the raw cycle threshold (Ct) values generated via quantitative reverse transcription polymerase chain reaction (qRT-PCR) to validate RNAi knockdown efficiency for hobbit-RNAi and *CG8671-RNAi *in Drosophila whole animals (WA) at 0 h after puparium formation (PF) using the ubiquitous act-GAL4 driver. Note that “>” in genotypes is shorthand for GAL4, UAS (e.g., act>hob(i) is short for act-GAL4 UAS-hob(i)).
Number of variables: 4
Number of header rows: 1
Number of rows: 6
Variable list:
Genotype (alphanumeric): the genotype and replicate number analyzed
rp49 Ct (numeric): cycle threshold (Ct) value for the reference gene rp49
hob Ct (numeric): cycle threshold (Ct) value for hob
CG8671 Ct (numeric): cycle threshold (Ct) value for CG8671
Data type: alphanumeric, numeric
Figure7HPupaVolumeData.csv
This file contains the raw data used to calculate body size/pupa volume in control (act>/+), ubiquitous hob-RNAi knockdown (act>hob(i)), and ubiquitous CG8671-RNAi knockdown (act>CG8671(i)). The length and width of each pupa (in mm) were measured in Adobe Photoshop CS6, and pupa volume was calculated using a published formula. Note that “>” in genotypes is shorthand for GAL4, UAS (e.g., act>hob(i) is short for act-GAL4 UAS-hob(i)).
Number of variables: 3
Number of header rows: 2
Number of rows: 100
Variable list:
Genotype (alphanumeric): the genotype being analyzed
pupa width (mm) (numeric): the measured width of each pupa
pupa length (mm) (numeric): the measured length of each pupa
Data type: alphanumeric, numeric
Code/software
Data are provided as .csv files, which can be opened by any freely available word processing software.
