Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 451

The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.

Female Gametophyte Development

Open access
Yadegari, R.·2004·THE PLANT CELL ONLINE

Abstract

Early in their evolution, plants acquired a life cycle that alternates between a multicellular haploid organism, the gametophyte, and a multicellular diploid organism, the sporophyte. Angiosperms have both female and male gametophytes. The female gametophyte is critical to many steps of the angiosperm reproductive process, including pollen tube guidance, fertilization, the induction of seed development upon fertilization, and maternal control of seed development after fertilization. Genetic analysis in Arabidopsis and maize has revealed mutants defective in almost all stages of female gametophyte development, and analysis of these mutants is beginning to reveal features of the female gametophyte developmental program. In addition, mutants defective in female gametophyte function have revealed regulatory genes required for the induction of endosperm development. From these studies, we are beginning to understand the regulatory networks involved in female gametophyte development and function. Gametophytes and sporophytes differ morphologically and functionally. The major function of diploid sporophyte generation is to produce haploid spores, which are the products of meiosis. Spores undergo cell proliferation and differentiation to develop into gametophytes. The major function of gametophyte generation is to produce haploid gametes. The fusion of egg and sperm gives rise to the zygote, which is the beginning of diploid sporophyte generation, thereby completing the life cycle (Gifford and Foster, 1989). The Arabidopsis Female Gametophyte. (A) Ovule. (B) Female gametophyte. The view in (B) is perpendicular to that in (A). The mature female gametophyte in Arabidopsis is ∼105 μm long and ∼25 μm wide. The gray areas represent cytoplasm, the white areas represent vacuoles, and the black areas represent nuclei. ac, antipodal cells; cc, central cell; ch, chalazal region of the ovule; ec, egg cell; f, funiculus; mp, micropyle; sc, synergid cell; sn, secondary nucleus. The angiosperm gametophytes are essential for the reproductive process. During sexual reproduction in angiosperms, the male gametophyte is transferred from the anther to the carpel's stigma, whereupon it forms a pollen tube that grows great distances through the carpel's internal tissues to deliver its two sperm cells to the female gametophyte. One sperm cell fertilizes the egg cell and the second sperm cell fuses with the central cell. After fertilization, the ovule gives rise to a seed; the seed's embryo, endosperm, and seed coat are derived from the fertilized egg cell, fertilized central cell, and ovule integuments, respectively (Maheshwari, 1950). The female gametophyte plays a critical role in essentially every step of the reproductive process. During pollen tube growth, the female gametophyte participates in directing the pollen tube to the ovule (Higashiyama, 2002; Johnson and Preuss, 2002; Higashiyama et al., 2003). During fertilization, cytoskeletal components within the female gametophyte direct the sperm cells to the egg cell and the central cell (Russell, 1992, 1993; Lord and Russell, 2002). Upon fertilization, female gametophyte–expressed genes control the initiation of seed development (Chaudhury et al., 2001). During seed development, female gametophyte–expressed gene products play a role in controlling embryo and endosperm development (Ray, 1997; Chaudhury and Berger, 2001). In this review, we describe angiosperm female gametophyte structure and development, summarize the female gametophyte's reproductive functions, and discuss the molecular and genetic approaches that are being used to understand these processes at the molecular level. Comprehensive reviews of the female gametophyte have been published previously (Maheshwari, 1950; Willemse and van Went, 1984; Haig, 1990; Huang and Russell, 1992; Russell, 2001). Patterns of Female Gametophyte Development Exhibited by Angiosperms. Genera exhibiting these patterns are indicated in parentheses. More comprehensive descriptions of the variation among angiosperms can be found in several reviews (Maheshwari, 1950; Willemse and van Went, 1984; Haig, 1990; Huang and Russell, 1992; Russell, 2001). In this figure, the chalazal end of the female gametophyte is up and the micropylar end is down. FG, female gametophyte. During megasporogenesis, the diploid megaspore mother cell undergoes meiosis and gives rise to four haploid nuclei. Angiosperms exhibit three main patterns of megasporogenesis, referred to as monosporic, bisporic, and tetrasporic. These three patterns are summarized in Figure 2. The three types differ mainly in whether cell plate formation occurs after these divisions, thus determining the number of meiotic products that contribute to the formation of the mature female gametophyte. In the monosporic pattern, both meiotic divisions are accompanied by cell plate formation, resulting in four one-nucleate megaspores. Subsequently, three megaspores, generally the micropylar-most megaspores

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1105/tpc.018192

Cites

38 of 38 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Cited by

See all 451

Metadata

Authors
Yadegari, R.
Venue
THE PLANT CELL ONLINE
Published
2004-03-12
Volume
16
Issue
suppl_1
Pages
S133-S141
ISSN
  • 1040-4651 (ISSN-L)
  • 1532-298X
OpenAlex
W2058185970
Cited by
451
References
38
FWCI
8.64
Type
journal article
Language
en
Open access
bronze

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.