Double fertilization is a complex fertilization mechanism that has evolved in flowering plants, known as angiosperms. This process involves the joining of a female gametophyte (embryo sac) with two male gametes (sperm). It begins when a pollen grain adheres to the stigma of the carpel, the female reproductive structure of a flower. After a pollen grain has landed on an accessible stigma, the pollen grain takes in moisture and begins to germinate, forming a pollen tube that extends down toward the ovary through the style. The tip of the pollen tube then enters the ovary and penetrates through the micropyle. The micropyle is an opening in the protective layers of the ovule. The pollen tube proceeds to release the two sperm in or near the embryo sac.
One sperm fertilizes the egg cell and the other sperm combines with the two polar nuclei of the large central cell of the embryo sac. The sperm and haploid egg combine to form a diploid zygote, while the other sperm and two haploid polar nuclei form a triploid nucleus (some plants may form polyploid nuclei). The large cell of the embryo sac will then form the endosperm, a nutrient-rich tissue which provides nourishment to the developing embryo. The ovary, surrounding the ovules, develops into the fruit, which is used for protection and dispersion of the seeds. 
The two central cell maternal nuclei (polar nuclei) that contribute to the endosperm, arise by mitosis from a single meiotic product. Therefore, maternal contribution to the genetic constitution of the triploid endosperm is different from that of the embryo.
In a recent study done of the plant Arabidopsis thaliana, the migration of male nuclei inside the female gamete, in fusion with the female nuclei, has been documented for the first time using in vivo imaging. Identification of the genes involved in the migration and fusion process has also been determined. For the complete study and the steps captured by in vivo imaging please refer to the article "Double Fertilization - Caught in the Act", referenced below. 
 Brief history
Double fertilization was discovered more than a century ago by Sergius Nawaschin in St. Petersburg, Russia, and Léon Guignard in France. Each made the discovery independently of the other. Lilium martagon and Fritillaria tenella were used in the first observations of double fertilization, which were made using the classical light microscope. Due to the limitations of the light microscope, there were many unanswered questions regarding the process of double fertilization. However, with the development of the electron microscope, many of the questions were answered. Most notably, the observations made by the group of W. Jensen showed that the male gametes did not have any cell walls and that the plasma membrane of the gametes is in close proximity to the plasma membrane of the cell that surrounds them inside the pollen grain.
 In vitro double fertilization
In vitro double fertilization is often used to study the molecular interactions as well as other aspects of gamete fusion in flowering plants. One of the major obstacles in developing an in vitro double fertilization between male and female gametes is the confinement of the sperm in the pollen tube and the egg in the embryo sac. A controlled fusion of the egg and sperm has already been achieved with poppy plants.  Pollen germination, pollen tube entry, and double fertilization processes have all been observed to proceed normally. In fact, this technique has already been used to obtain seeds in various flowering plants and was named 'test-tube fertilization'. 
The female gametophyte, or megagametophyte, used in double fertilization is the embryo sac. This develops within an ovule, enclosed by the ovary at the base of a carpel. Surrounding the embryo sac are two integuments, which form an opening called the micropyle. The embryo sac, which is primarily haploid, originates from the diploid megaspore mother cell within the ovule. The megasporocyte undergoes a meiotic cell division, producing four haploid megaspores. The next sequence of events varies, depending on the particular species. However, in most angiosperm species, only one of the four resulting megaspores survives. This megaspore undergoes three rounds of mitotic division, resulting in one large cell with eight haploid nuclei. Membranes then divide this mass into a muticellular female gametophyte, called the embryo sac. The lower end of the embryo sac consists of the haploid egg cell positioned in the middle of two other haploid cells, called synergids. The synergids function in the attraction and guidance of the pollen tube to the embryo sac through the micropyle. At the upper end of the embryo sac are three antipodal cells. The remaining two nuclei, called polar nuclei, share the cytoplasm of the large central cell of the embryo sac, rather than being partitioned into separate cells.
The male gametophytes, or microgametophytes, used in double fertilization are pollen grains. They develop within the microsporangia, or pollen sacs, of anthers at the tips of the stamens. Each microsporangia contains diploid microspore mother cells, or microsporocytes. Each microsporocyte undergoes meiosis, forming four haploid microspores, each of which can eventually develop into a pollen grain. A microspore undergoes mitosis and cytokinesis in order to produce two separate cells, the generative cell and the tube cell. These two cells in addition to the spore wall make up an immature pollen grain. As the male gametophyte matures, the generative cell passes into the tube cell, and the tube cell produces the pollen tube. Once the pollen grain has matured, the anthers break open, releasing the pollen. The pollen is carried to the stigma of another flower, by wind or animal pollinators, and deposited on the pistil. As the pollen grain germinates, the pollen tube elongates, and the generative cell undergoes mitosis, producing two sperm cells. The pollen tube extends down the long style of the carpel and into the ovary, where its sperm cells are released near the embryo sac. Double fertilization proceeds from here. 
 See also
- ^ Berger, F. (January 2008). "Double-fertilization, from myths to reality". Sex Plant Reprod 21: 3'5. doi:10.1007/s00497-007-0066-4.
- ^ Berger, F. & Hamamura, Y. & Ingouff, M. & Higashiyama, T. (August 2008). "Double fertilization ' Caught In The Act". Trends in Plant Science 13 (8): 437'443. doi:10.1016/j.tplants.2008.05.011. PMID 18650119.
- ^ Jensen, W. A. (February 1998). "Double Fertilization: A Personal View". Sexual Plant Reproduction 11 (1): 1'5. doi:10.1007/s004970050113.
- ^ Dumas, C., & Rogowsky, P. (August 2008). "Fertilization and Early Seed Formation". Compres Rendus Biologies 331 (10): 715'725. doi:10.1016/j.crvi.2008.07.013. PMID 18926485.
- ^ Zenkteler, M. (1990). "In vitro fertilization and wide hybridization in higher plants". Crit Rev Plant Sci 9: 267'279. doi:10.1080/07352689009382290.
- ^ Raghavan, V. (2005). Double fertilization: embryo and endosperm development in flowering plants (illustrated ed.). Birkhäuser. pp. 17'19. ISBN 3540277919.
- ^ Campbell N.A & Reece J.B (2005). Biology (7 ed.). San Francisco, CA: Pearson Education, Inc.. pp. 774'777. ISBN 0-8053-7171-0.
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