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Photoreceptors detect light, with phytochromes (PHY) specifically monitoring red and far-red wavelengths.\n                      <jats:italic>Arabidopsis thaliana<\/jats:italic>\n                      has five phytochromes, named phyA through phyE. phyA and phyB are extensively studied key mediators of most phytochrome responses; the precise functions of the other phytochromes remain poorly understood. To investigate phyD signaling, we overexpressed phyD-YFP alone and together with phyB-CFP in a genetic background lacking other phytochromes. Photomorphogenic responses, protein accumulation, and transcriptome changes were compared at low and high temperatures. We found that phyD-YFP alone cannot facilitate photomorphogenesis, but it significantly promotes red light signaling of both phyB-CFP and endogenous phyB in a temperature-dependent manner, being effective at low but not at high temperatures. In parallel, co-expressing phyD-YFP and phyB-CFP triggered substantially more robust light-induced transcriptome changes at low temperatures than expressing either transgene alone. Because phyD-YFP is more light-stable than phyB, and both PHYB-CFP and endogenous PHYB accumulate to higher levels alongside PHYD-YFP in light, phyD likely stimulates phyB signaling via PHYB protein stabilization. To explain how PHYD-YFP enhances PHYB levels at both temperatures yet stimulates signaling exclusively at low temperatures, we propose that phyD and phyB form light-stable heterodimers at both temperatures and that these heterodimers are functional only at low temperatures. Our findings demonstrate that phyB and phyD functionally cooperate to mediate temperature-dependent light signaling responses, providing plants with developmental flexibility under changing environmental conditions.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1007\/s00299-026-04025-y","type":"journal-article","created":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T04:10:54Z","timestamp":1792728654000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Transgenic phytochrome D cooperates with phytochrome B to promote photomorphogenesis at low temperatures"],"prefix":"10.1007","volume":"45","author":[{"given":"Lilla","family":"S\u00edpos","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G\u00e1bor","family":"Gr\u00e9zal","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Csaba","family":"P\u00e9ter","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ferenc","family":"Nagy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D\u00e1niel","family":"Silhavy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2055-3430","authenticated-orcid":false,"given":"Andr\u00e1s","family":"Viczi\u00e1n","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2026,10,23]]},"reference":[{"key":"4025_CR1","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1111\/nph.12364","volume":"200","author":"\u00c9 \u00c1d\u00e1m","year":"2013","unstructured":"\u00c1d\u00e1m \u00c9, Kircher S, Liu P, M\u00e9rai Z, Gonz\u00e1lez-Schain N, H\u00f6rner M, Viczi\u00e1n A, Monte E, Sharrock RA, Sch\u00e4fer E et al (2013) Comparative functional analysis of full-length and N-terminal fragments of phytochrome C, D and E in red light-induced signaling. 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