The C‐terminal region of <scp>KIF26B</scp> is indispensable for nephron progenitor condensation and kidney formation in mice

Loss of Kif26b function causes renal agenesis or hypoplasia in mice, and a KIF26B mutation resulting in deletion of the C-terminal region has been identified in a human patient with a congenital kidney disorder. However, the role of this region during kidney development is unclear; thus, to investigate this, we generated mice lacking the C-terminal region of KIF26B (Kif26b-C) using CRISPR/Cas9. Homozygous Kif26b-C mice showed bilateral renal agenesis, resembling Kif26b knockout mice. Histological analysis revealed loss of the nephrogenic zone and impaired nephron progenitor condensation at embryonic day 18.5. In situ hybridization showed reduced Gdnf in the metanephric mesenchyme and reduced Wnt11 in ureteric buds, indicating disruption of the Gdnf-Wnt11 signaling loop. These findings suggest a key role for the KIF26B C-terminal region in kidney morphogenesis.

Authors

Institutions

Publication Details

Journal
FEBS Open Bio
Published
2026-05-18
DOI
https://doi.org/10.1002/2211-5463.70260
Primary Topic
Renal and related cancers
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The C‐terminal region of KIF26B is indispensable for nephron progenitor condensation and kidney formation in mice

Hiroshi Kawasaki, Kengo Furuichi, Sako Keisuke, Akihiko Koshino et al.
FEBS Open Bio
Renal and related cancers
article

The C‐terminal region of KIF26B is indispensable for nephron progenitor condensation and kidney formation in mice

Hiroshi Kawasaki, Kengo Furuichi, Sako Keisuke, Akihiko Koshino, Yohei Shinmyo, Minako Yamamura, Taichiro Minami, Megumi Oshima, Yuta Yamamura, Norihiko Sakai, Miho Shimizu, Takiko Daikoku, Akinori Hara, Shin‐ichi Horike, H Akamatsu, Kenta Takahashi, Takashi Wada, Kenichi Harada, Yasunori Iwata, Naoki Yamamoto
article en

Abstract

Loss of Kif26b function causes renal agenesis or hypoplasia in mice, and a KIF26B mutation resulting in deletion of the C-terminal region has been identified in a human patient with a congenital kidney disorder. However, the role of this region during kidney development is unclear; thus, to investigate this, we generated mice lacking the C-terminal region of KIF26B (Kif26b-C) using CRISPR/Cas9. Homozygous Kif26b-C mice showed bilateral renal agenesis, resembling Kif26b knockout mice. Histological analysis revealed loss of the nephrogenic zone and impaired nephron progenitor condensation at embryonic day 18.5. In situ hybridization showed reduced Gdnf in the metanephric mesenchyme and reduced Wnt11 in ureteric buds, indicating disruption of the Gdnf-Wnt11 signaling loop. These findings suggest a key role for the KIF26B C-terminal region in kidney morphogenesis.

FEBS Open Bio
Kanazawa University (JP), Kanazawa Medical University (JP), Hamamatsu University School of Medicine (JP), Model Animal Research Center (CN), Institute for Disease Modeling (US)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Openalex Percentile: Top 8%
Renal and related cancers
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.