» Articles » PMID: 38931095

Morphological Study on the Differentiation of Flower Buds and the Embryological Stages of Male and Female Floral Organs in (Laxm.) Schindl. Cv. JinNong ()

Overview
Journal Plants (Basel)
Date 2024 Jun 27
PMID 38931095
Authors
Affiliations
Soon will be listed here.
Abstract

(Laxm.) is a leguminous plant with significant ecological benefits, but its embryonic development mechanism remains unclear. We investigated the flower bud differentiation, megaspore and microspore formation, gametophyte development, and embryo and endosperm development in . Our aim was to elucidate the relationship between the external morphology and internal development processes of male and female floral organs during growth, as well as the reproductive factors influencing fruiting. The results indicated that although the pistil develops later than the stamen during flower bud differentiation, both organs mature synchronously before flowering. pollen exhibits three germination grooves, a reticulate outer wall, and papillary structures on the anther surface. In vivo pollination experiments revealed abnormal spiral growth of pollen tubes within the style and the occurrence of callus plugs, which may reduce the seed setting rate. The anther wall development follows the dicotyledonous type, with tetrads formed through microspore meiosis exhibiting both left-right symmetry and tetrahedral arrangements. has a single ovule, and the embryo sac develops in the monosporic polygonum type. After dormancy, the zygote undergoes multiple divisions, progressing through spherical, heart-shaped, and torpedo-shaped embryo stages, culminating in a mature embryo. A mature seed comprises cotyledons, hypocotyl, embryo, radicle, and seed coat. Phylogenetic tree analysis reveals a close genetic relationship between and other leguminous plants from the genera and . This study provides valuable insights into the regulation of flowering and hybrid breeding in leguminous plants and offers a new perspective on the development of floral organs and seed setting rates.

References
1.
Wang Y, Li X, Fan B, Zhu C, Chen Z . Regulation and Function of Defense-Related Callose Deposition in Plants. Int J Mol Sci. 2021; 22(5). PMC: 7957820. DOI: 10.3390/ijms22052393. View

2.
Johnson M, Preuss D . Plotting a course: multiple signals guide pollen tubes to their targets. Dev Cell. 2002; 2(3):273-81. DOI: 10.1016/s1534-5807(02)00130-2. View

3.
Gonzalez-Melendi P, Uyttewaal M, Morcillo C, Hernandez Mora J, Fajardo S, Budar F . A light and electron microscopy analysis of the events leading to male sterility in Ogu-INRA CMS of rapeseed (Brassica napus). J Exp Bot. 2008; 59(4):827-38. DOI: 10.1093/jxb/erm365. View

4.
Haruta M, Sabat G, Stecker K, Minkoff B, Sussman M . A peptide hormone and its receptor protein kinase regulate plant cell expansion. Science. 2014; 343(6169):408-11. PMC: 4672726. DOI: 10.1126/science.1244454. View

5.
Zhong S, Li L, Wang Z, Ge Z, Li Q, Bleckmann A . RALF peptide signaling controls the polytubey block in . Science. 2022; 375(6578):290-296. PMC: 9040003. DOI: 10.1126/science.abl4683. View