Scholarlink

<p>The Keap1/Nrf2 signaling pathway is a master regulator of cellular defense against oxidative and electrophilic stress. In teleosts like zebrafish (<i>Danio rerio</i>), whole-genome duplication resulted in two <i>keap1</i> paralogs, <i>keap1a</i> and <i>keap1b</i>, whose functional specificities remain incompletely understood. This study investigates the divergent roles of these paralogs by comparing the responses of established keap1a and novel keap1b knockout larvae to distinct chemical stressors. By comparing the responses of <i>keap1b</i><sup><i>dl40</i></sup>, <i>keap1a</i><sup><i>dl07</i></sup>, and <i>nfe2l2a</i><sup><i>dl703</i></sup> (Nrf2a) larvae to these stressors, we uncovered a striking functional dichotomy. While loss of either paralog conferred resistance to H₂O₂-induced oxidative stress, <i>keap1b</i><sup><i>dl40</i></sup> larvae, unlike their <i>keap1a</i><sup><i>dl07</i></sup> counterparts, exhibited extreme sensitivity to the lethal effects of CuSO₄ exposure, with survival rates plummeting to ~ 25%. This heightened sensitivity to copper sulfate was associated with a blunted transcriptional response of inflammatory markers <i>tnf-a</i> and <i>c3a</i>, suggesting that Keap1b is critical for modulating the Nrf2a-mediated response to inflammatory stress in orchestrating a viable inflammatory response. This work clarifies the non-redundant, vital function of Keap1b in the response to heavy metal-induced stress and provides a valuable genetic resource (<i>keap1b</i><sup><i>dl40</i></sup> null allele) for future studies.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Functional divergence of zebrafish keap1 paralogs revealed by CRISPR/Cas9-mediated gene editing: a specialized role for keap1b in inflammation

  • 期刊论文

  • 发表日期：

    2025年12月8日

查看全文
  • Vu Thanh Nguyen,
  • Bui Thi Thu Van,
  • Tran Ngoc Uyen,
  • Nguyen Xuan Tong,
  • Thanh Luu Pham,
  • Nguyen Hoang Thuy Vy,
  • Dinh Thi Thuy,
  • Nguyen Phuong Thuy,
  • Makoto Kobayashi

摘要

The Keap1/Nrf2 signaling pathway is a master regulator of cellular defense against oxidative and electrophilic stress. In teleosts like zebrafish (Danio rerio), whole-genome duplication resulted in two keap1 paralogs, keap1a and keap1b, whose functional specificities remain incompletely understood. This study investigates the divergent roles of these paralogs by comparing the responses of established keap1a and novel keap1b knockout larvae to distinct chemical stressors. By comparing the responses of keap1bdl40, keap1adl07, and nfe2l2adl703 (Nrf2a) larvae to these stressors, we uncovered a striking functional dichotomy. While loss of either paralog conferred resistance to H₂O₂-induced oxidative stress, keap1bdl40 larvae, unlike their keap1adl07 counterparts, exhibited extreme sensitivity to the lethal effects of CuSO₄ exposure, with survival rates plummeting to ~ 25%. This heightened sensitivity to copper sulfate was associated with a blunted transcriptional response of inflammatory markers tnf-a and c3a, suggesting that Keap1b is critical for modulating the Nrf2a-mediated response to inflammatory stress in orchestrating a viable inflammatory response. This work clarifies the non-redundant, vital function of Keap1b in the response to heavy metal-induced stress and provides a valuable genetic resource (keap1bdl40 null allele) for future studies.