Histopathology image classification: Highlighting the gap between manual analysis and AI automation

Zygote
Zygote formation: egg cell after fertilization with a sperm. The male and female pronuclei are converging, but the genetic material is not yet united.
Details
Days	0
Precursor	Gametes
Gives rise to	Blastomeres
Identifiers
MeSH	D015053
TE	E2.0.1.2.0.0.9
FMA	72395
Anatomical terminology [edit on Wikidata]

Part of a series on
Human growth and development
Stages
Gamete Zygote Embryo Fetus Infant Toddler Child Preadolescent Adolescent Emerging and early adulthood Young adult Middle adult Old adult Dying
Biological milestones
Fertilization Pregnancy Childbirth Walking Language acquisition Puberty Menopause Ageing Death
Development and psychology
Pre- and perinatal Infant and child Nature versus nurture Adolescent Youth Young adult Adult Maturity
Developmental stage theories
Attachment Ecological Psychosocial Psychosexual development Moral Cognitive Cultural-historical Evolutionary
Psychology portal

A zygote (/ˈzaɪˌɡoʊt/; from Ancient Greek ζυγωτός (zygōtós) 'joined, yoked', from ζυγοῦν (zygoun) 'to join, to yoke')^[1] is a eukaryotic cell formed by a fertilization event between two gametes. The zygote's genome is a combination of the DNA in each gamete, and contains all of the genetic information of a new individual organism. The sexual fusion of haploid cells is called karyogamy, the result of which is the formation of a diploid cell called the zygote or zygospore.

German zoologists Oscar and Richard Hertwig made some of the first discoveries on animal zygote formation in the late 19th century.

The zygote is the earliest developmental stage. In humans and most other anisogamous organisms, a zygote is formed when an egg cell and sperm cell come together to create a new unique organism.

The formation of a totipotent zygote with the potential to produce a whole organism depends on epigenetic reprogramming. DNA demethylation of the paternal genome in the zygote appears to be an important part of epigenetic reprogramming.^[2] In the paternal genome of the mouse, demethylation of DNA, particularly at sites of methylated cytosines, is likely a key process in establishing totipotency. Demethylation involves the processes of base excision repair and possibly other DNA-repair–based mechanisms.^[2]

In human fertilization, a released ovum (a haploid secondary oocyte with replicate chromosome copies) and a haploid sperm cell (male gamete) combine to form a single diploid cell called the zygote. Once the single sperm fuses with the oocyte, the latter completes the division of the second meiosis forming a haploid daughter with only 23 chromosomes, almost all of the cytoplasm, and the male pronucleus. The other product of meiosis is the second polar body with only chromosomes but no ability to replicate or survive. In the fertilized daughter, DNA is then replicated in the two separate pronuclei derived from the sperm and ovum, making the zygote's chromosome number temporarily 4n diploid. After approximately 30 hours from the time of fertilization, a fusion of the pronuclei and immediate mitotic division produce two 2n diploid daughter cells called blastomeres.^[3] Between the stages of fertilization and implantation, the developing embryo is sometimes termed as a preimplantation-conceptus. This stage has also been referred to as the pre-embryo in legal discourses including relevance to the use of embryonic stem cells.^[4] In the US the National Institutes of Health has determined that the traditional classification of pre-implantation embryo is still correct.^[5]

After fertilization, the conceptus travels down the fallopian tube towards the uterus while continuing to divide^[6] without actually increasing in size, in a process called cleavage.^[7] After four divisions, the conceptus consists of 16 blastomeres, and it is known as the morula.^[8] Through the processes of compaction, cell division, and blastulation, the conceptus takes the form of the blastocyst by the fifth day of development, just as it approaches the site of implantation.^[9] When the blastocyst hatches from the zona pellucida, it can implant in the endometrial lining of the uterus and begin the gastrulation stage of embryonic development.

The human zygote has been genetically edited in experiments designed to cure inherited diseases.^[10]

In fungi, this cell may then enter meiosis or mitosis depending on the life cycle of the species.^{[citation needed]}

In plants, the zygote may be polyploid if fertilization occurs between meiotically unreduced gametes.

In land plants, the zygote is formed within a chamber called the archegonium. In seedless plants, the archegonium is usually flask-shaped, with a long hollow neck through which the sperm cell enters. As the zygote divides and grows, it does so inside the archegonium.^{[citation needed]}

The zygote can divide asexually by mitosis to produce identical offspring.^{[citation needed]}

A Chlamydomonas zygote contains chloroplast DNA (cpDNA) from both parents; such cells are generally rare, since normally cpDNA is inherited uniparentally from the mt+ mating type parent. These rare biparental zygotes allowed mapping of chloroplast genes by recombination.^{[citation needed]}

• Breastfeeding and fertility
• Fertilization
• Proembryo