scholarly journals The TRAF Mediated Gametogenesis Progression (TRAMGaP) Gene Is Required for Megaspore Mother Cell Specification and Gametophyte Development

2017 ◽  
Vol 175 (3) ◽  
pp. 1220-1237 ◽  
Author(s):  
Sunil Kumar Singh ◽  
Vajinder Kumar ◽  
Ramamurthy Srinivasan ◽  
Paramvir Singh Ahuja ◽  
Shripad Ramchandra Bhat ◽  
...  
1962 ◽  
Vol 10 (1) ◽  
pp. 1 ◽  
Author(s):  
GL Davis

Cotula australis has a discoid heterogamous capitulum in which the outermost three whorls of florets are female and naked. The bisexual disk florets are fully fertile and have a four-lobed corolla with four shortly epipetalous stamens. The anthers contain only two microsporangia. Wall formation and microsporogenesis are described and the pollen grains are shed at the three-celled condition. The ovule is teguinucellate and the hypodermal archesporial cell develops directly as the megaspore mother cell. Megasporogenesis is normal and the monosporio embryo sac develops from the chalazal megaspore. Breakdown of the nucellar epidermis takes place when the embryo sac is binucleate and its subsequent development follows the Polygonum type. The synergids extend deeply into the micropyle and one persists until late in embryogeny as a haustorium. The development of the embryo is of the Asterad type, and the endosperm is cellular. C. coronopifolia agrees with C. australis in the presence of only two microsporangia in each anther and the development of a synergid haustorium.


2019 ◽  
Vol 20 (12) ◽  
pp. 3051 ◽  
Author(s):  
Vasily V. Ashapkin ◽  
Lyudmila I. Kutueva ◽  
Nadezhda I. Aleksandrushkina ◽  
Boris F. Vanyushin

Unlike in animals, the reproductive lineage cells in plants differentiate from within somatic tissues late in development to produce a specific haploid generation of the life cycle—male and female gametophytes. In flowering plants, the male gametophyte develops within the anthers and the female gametophyte—within the ovule. Both gametophytes consist of only a few cells. There are two major stages of gametophyte development—meiotic and post-meiotic. In the first stage, sporocyte mother cells differentiate within the anther (pollen mother cell) and the ovule (megaspore mother cell). These sporocyte mother cells undergo two meiotic divisions to produce four haploid daughter cells—male spores (microspores) and female spores (megaspores). In the second stage, the haploid spore cells undergo few asymmetric haploid mitotic divisions to produce the 3-cell male or 7-cell female gametophyte. Both stages of gametophyte development involve extensive epigenetic reprogramming, including siRNA dependent changes in DNA methylation and chromatin restructuring. This intricate mosaic of epigenetic changes determines, to a great extent, embryo and endosperm development in the future sporophyte generation.


1974 ◽  
Vol 52 (4) ◽  
pp. 885-893 ◽  
Author(s):  
Elizabeth A. Stanlake ◽  
John N. Owens

A morphological study of the female gametophyte and embryo development was made for western hemlock (Tsuga heterophylla (Raf.) Sarg.) growing in the Victoria, B.C., area. Western hemlock follows a pattern of development similar to other members of the Pinaceae. A comparison was also made between development in western hemlock and other gymnosperm families. Meiosis of the megaspore mother cell in western hemlock begins in early February and is completed at the end of the first week in March. This is 3 weeks before pollination. Fertilization occurs 6 weeks after pollination, in the middle of May. Embryo development takes place throughout June and July and the embryo is mature by the middle of August. Seed fall occurs throughout September, 5 months after pollination.


1986 ◽  
Vol 16 (6) ◽  
pp. 1301-1309 ◽  
Author(s):  
Grzegorz Kosiński

The phenology of sexual reproduction in Larixdecidua Mill, varies from year to year, and some intra- and inter-clonal differences were also found. Megaspore mother cell meiosis occurred at the time of pollination, during the second half of April, resulting in three or four megaspores. The free nuclear stage and cell wall and archegonia formation were completed in late May and the first half of June. An average of four archegonia was observed in each ovule, but the number ranged from two to six. Fertilization occurred during the first 20 days of June, about 7 weeks after pollination. A four-tiered, 16-celled proembryo formed. Meristematic regions formed in the embryo from the end of June to mid-July. Fully developed embryos were observed in mid-August. Simple polyembryony and delayed cleavage polyembryony were observed. Lack of pollination, disturbances during megasporogenesis and female gametophyte development, failure of fertilization, and embryo degeneration are the major factors resulting in empty seed.


Development ◽  
2000 ◽  
Vol 127 (1) ◽  
pp. 197-207 ◽  
Author(s):  
I. Siddiqi ◽  
G. Ganesh ◽  
U. Grossniklaus ◽  
V. Subbiah

In higher plants the gametophyte consists of a gamete in association with a small number of haploid cells, specialized for sexual reproduction. The female gametophyte or embryo sac, is contained within the ovule and develops from a single cell, the megaspore which is formed by meiosis of the megaspore mother cell. The dyad mutant of Arabidopsis, described herein, represents a novel class among female sterile mutants in plants. dyad ovules contain two large cells in place of an embryo sac. The two cells represent the products of a single division of the megaspore mother cell followed by an arrest in further development of the megaspore. We addressed the question of whether the division of the megaspore mother cell in the mutant was meiotic or mitotic by examining the expression of two markers that are normally expressed in the megaspore mother cell during meiosis. Our observations indicate that in dyad, the megaspore mother cell enters but fails to complete meiosis, arresting at the end of meiosis 1 in the majority of ovules. This was corroborated by a direct observation of chromosome segregation during division of the megaspore mother cell, showing that the division is a reductional and not an equational one. In a minority of dyad ovules, the megaspore mother cell does not divide. Pollen development and male fertility in the mutant is normal, as is the rest of the ovule that surrounds the female gametophyte. The embryo sac is also shown to have an influence on the nucellus in wild type. The dyad mutation therefore specifically affects a function that is required in the female germ cell precursor for meiosis. The identification and analysis of mutants specifically affecting female meiosis is an initial step in understanding the molecular mechanisms underlying early events in the pathway of female reproductive development.


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