Haustorial processes during the female gametophyte formation in Rosularia pallida (Schott & Kotschy) Stapf (Crassulaceae).

IF 2.9 4区 生物学 Q2 PLANT SCIENCES
Emilia Brzezicka, Małgorzata Kozieradzka-Kiszkurno
{"title":"Haustorial processes during the female gametophyte formation in Rosularia pallida (Schott & Kotschy) Stapf (Crassulaceae).","authors":"Emilia Brzezicka, Małgorzata Kozieradzka-Kiszkurno","doi":"10.1007/s00497-025-00521-5","DOIUrl":null,"url":null,"abstract":"<p><strong>Key message: </strong>Ultrastructural and cytochemical analyses of the megaspore, embryo sac, and synergid haustoria reveal their roles in nutrition, contributing to the successful development of the megagametophyte in R. pallida. In this paper, we present the first cytochemical and ultrastructural analysis of the megaspores, embryo sac, and synergid haustoria in Rosularia pallida (Schott & Kotschy) Stapf (Crassulaceae) are presented. The haustoria in the ovule of R. pallida primarily function to provide nutrition during megasporogenesis and megagametogenesis. Cytochemical staining reveals a significant increase in the accumulation of insoluble polysaccharides, lipids, and proteins within the megaspores and embryo sac. This increase occurs alongside the progressive degradation of nucellar cells and the growth of haustoria towards the integuments. The direction of haustorial growth within sporophyte tissues and the distribution of nutrients within the ovule complement each other, collectively contributing to efficient nutrition for the developing female gametophyte. Callose is present in the walls of both the megaspores and their haustoria. The functional megaspore (FM) haustorium is the only one that extends beyond the nucellus into the integuments during megasporogenesis. The disappearance of callose in the micropylar portion of the FM haustorium enables apoplasmic transport, particularly in this region. These findings suggest that the FM haustorium supports the development of a specific megaspore in the tetrad, indirectly influencing FM selection through nutrient provision. Furthermore, the removal of callose on the chalazal side of the tetrad likely facilitates the development of the embryo sac from the chalazal megaspore. Ultrastructural analyses of the megaspore, embryo sac, and synergid haustoria reveal the presence of transfer-wall ingrowths. No plasmodesmata were detected in the haustorial walls. Additionally, ultrastructural observations of the synergids indicate that their haustorium significantly elongates toward the micropyle and becomes metabolically active.</p>","PeriodicalId":51297,"journal":{"name":"Plant Reproduction","volume":"38 2","pages":"11"},"PeriodicalIF":2.9000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00497-025-00521-5","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Key message: Ultrastructural and cytochemical analyses of the megaspore, embryo sac, and synergid haustoria reveal their roles in nutrition, contributing to the successful development of the megagametophyte in R. pallida. In this paper, we present the first cytochemical and ultrastructural analysis of the megaspores, embryo sac, and synergid haustoria in Rosularia pallida (Schott & Kotschy) Stapf (Crassulaceae) are presented. The haustoria in the ovule of R. pallida primarily function to provide nutrition during megasporogenesis and megagametogenesis. Cytochemical staining reveals a significant increase in the accumulation of insoluble polysaccharides, lipids, and proteins within the megaspores and embryo sac. This increase occurs alongside the progressive degradation of nucellar cells and the growth of haustoria towards the integuments. The direction of haustorial growth within sporophyte tissues and the distribution of nutrients within the ovule complement each other, collectively contributing to efficient nutrition for the developing female gametophyte. Callose is present in the walls of both the megaspores and their haustoria. The functional megaspore (FM) haustorium is the only one that extends beyond the nucellus into the integuments during megasporogenesis. The disappearance of callose in the micropylar portion of the FM haustorium enables apoplasmic transport, particularly in this region. These findings suggest that the FM haustorium supports the development of a specific megaspore in the tetrad, indirectly influencing FM selection through nutrient provision. Furthermore, the removal of callose on the chalazal side of the tetrad likely facilitates the development of the embryo sac from the chalazal megaspore. Ultrastructural analyses of the megaspore, embryo sac, and synergid haustoria reveal the presence of transfer-wall ingrowths. No plasmodesmata were detected in the haustorial walls. Additionally, ultrastructural observations of the synergids indicate that their haustorium significantly elongates toward the micropyle and becomes metabolically active.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Plant Reproduction
Plant Reproduction PLANT SCIENCES-REPRODUCTIVE BIOLOGY
CiteScore
6.30
自引率
2.90%
发文量
19
期刊介绍: Plant Reproduction (formerly known as Sexual Plant Reproduction) is a journal devoted to publishing high-quality research in the field of reproductive processes in plants. Article formats include original research papers, expert reviews, methods reports and opinion papers. Articles are selected based on significance for the field of plant reproduction, spanning from the induction of flowering to fruit development. Topics incl … show all
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信