Cargando…
Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies
Many animals use the Earth’s geomagnetic field for orientation and navigation. Yet, the molecular and cellular underpinnings of the magnetic sense remain largely unknown. A biophysical model proposed that magnetoreception can be achieved through quantum effects of magnetically-sensitive radical pair...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859408/ https://www.ncbi.nlm.nih.gov/pubmed/33536422 http://dx.doi.org/10.1038/s41467-021-21002-z |
_version_ | 1783646726385565696 |
---|---|
author | Wan, Guijun Hayden, Ashley N. Iiams, Samantha E. Merlin, Christine |
author_facet | Wan, Guijun Hayden, Ashley N. Iiams, Samantha E. Merlin, Christine |
author_sort | Wan, Guijun |
collection | PubMed |
description | Many animals use the Earth’s geomagnetic field for orientation and navigation. Yet, the molecular and cellular underpinnings of the magnetic sense remain largely unknown. A biophysical model proposed that magnetoreception can be achieved through quantum effects of magnetically-sensitive radical pairs formed by the photoexcitation of cryptochrome (CRY) proteins. Studies in Drosophila are the only ones to date to have provided compelling evidence for the ultraviolet (UV)-A/blue light-sensitive type 1 CRY (CRY1) involvement in animal magnetoreception, and surprisingly extended this discovery to the light-insensitive mammalian-like type 2 CRYs (CRY2s) of both monarchs and humans. Here, we show that monarchs respond to a reversal of the inclination of the Earth’s magnetic field in an UV-A/blue light and CRY1, but not CRY2, dependent manner. We further demonstrate that both antennae and eyes, which express CRY1, are magnetosensory organs. Our work argues that only light-sensitive CRYs function in animal light-dependent inclination-based magnetic sensing. |
format | Online Article Text |
id | pubmed-7859408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78594082021-02-11 Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies Wan, Guijun Hayden, Ashley N. Iiams, Samantha E. Merlin, Christine Nat Commun Article Many animals use the Earth’s geomagnetic field for orientation and navigation. Yet, the molecular and cellular underpinnings of the magnetic sense remain largely unknown. A biophysical model proposed that magnetoreception can be achieved through quantum effects of magnetically-sensitive radical pairs formed by the photoexcitation of cryptochrome (CRY) proteins. Studies in Drosophila are the only ones to date to have provided compelling evidence for the ultraviolet (UV)-A/blue light-sensitive type 1 CRY (CRY1) involvement in animal magnetoreception, and surprisingly extended this discovery to the light-insensitive mammalian-like type 2 CRYs (CRY2s) of both monarchs and humans. Here, we show that monarchs respond to a reversal of the inclination of the Earth’s magnetic field in an UV-A/blue light and CRY1, but not CRY2, dependent manner. We further demonstrate that both antennae and eyes, which express CRY1, are magnetosensory organs. Our work argues that only light-sensitive CRYs function in animal light-dependent inclination-based magnetic sensing. Nature Publishing Group UK 2021-02-03 /pmc/articles/PMC7859408/ /pubmed/33536422 http://dx.doi.org/10.1038/s41467-021-21002-z Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wan, Guijun Hayden, Ashley N. Iiams, Samantha E. Merlin, Christine Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title | Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title_full | Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title_fullStr | Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title_full_unstemmed | Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title_short | Cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
title_sort | cryptochrome 1 mediates light-dependent inclination magnetosensing in monarch butterflies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859408/ https://www.ncbi.nlm.nih.gov/pubmed/33536422 http://dx.doi.org/10.1038/s41467-021-21002-z |
work_keys_str_mv | AT wanguijun cryptochrome1mediateslightdependentinclinationmagnetosensinginmonarchbutterflies AT haydenashleyn cryptochrome1mediateslightdependentinclinationmagnetosensinginmonarchbutterflies AT iiamssamanthae cryptochrome1mediateslightdependentinclinationmagnetosensinginmonarchbutterflies AT merlinchristine cryptochrome1mediateslightdependentinclinationmagnetosensinginmonarchbutterflies |