Meiosis is preceded by one interphase consists of the G1, S, and also G2 phases, i beg your pardon are practically identical to the phases preceding mitosis. The G1 phase, which is also called the very first gap phase, is the very first phase that the interphase and also is focused on cabinet growth. The S step is the second phase the interphase, during which the DNA the the chromosomes is replicated. Finally, the G2 phase, additionally called the 2nd gap phase, is the 3rd and last phase of interphase; in this phase, the cell undergoes the final preparations for meiosis.

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During DNA duplication in the S phase, each chromosome is replicated to develop two the same copies, referred to as sister chromatids, the are hosted together at the centromere by cohesin proteins. Cohesin hold the chromatids together until anaphase II. The centrosomes, which space the structures that theorem the microtubules the the meiotic spindle, additionally replicate. This prepares the cell to enter prophase I, the very first meiotic phase.

Prophase I

Early in prophase I, before the chromosomes deserve to be seen clearly microscopically, the homologous chromosomes room attached at their tips to the nuclear envelope through proteins. As the nuclear envelope starts to break down, the proteins associated with homologous chromosomes bring the pair close to each other. (Recall that, in mitosis, homologous chromosomes perform not pair together. In mitosis, homologous chromosomes heat up end-to-end so that once they divide, each daughter cell receives a sister chromatid indigenous both members of the homologous pair.) The synaptonemal complex, a lattice of proteins between the homologous chromosomes, an initial forms at specific locations and also then spreads to cover the entire length the the chromosomes. The tight pairing that the homologous chromosomes is called synapsis. In synapsis, the gene on the chromatids the the homologous chromosomes are aligned precisely with each other. The synaptonemal facility supports the exchange that chromosomal segments between non-sister homologous chromatids, a process called crossing over. Cross over deserve to be it was observed visually ~ the exchange as chiasmata (singular = chiasma) (Figure 1).


Figure 1. Early in prophase I, homologous chromosomes come with each other to type a synapse. The chromosomes room bound tightly together and also in perfect alignment through a protein lattice dubbed a synaptonemal complicated and by cohesin proteins at the centromere.


In types such together humans, even though the X and also Y sex chromosomes are not homologous (most that their gene differ), they have a small an ar of homology that allows the X and Y chromosomes to pair up throughout prophase I. A partial synaptonemal complex develops only between the areas of homology.

Located at intervals follow me the synaptonemal facility are large protein assemblies called recombination nodules. These assemblies mark the points of later on chiasmata and also mediate the multistep procedure of crossover—or hereditary recombination—between the non-sister chromatids. Near the recombination nodule on every chromatid, the double-stranded DNA is cleaved, the cut ends room modified, and a brand-new connection is made in between the non-sister chromatids. Together prophase ns progresses, the synaptonemal complex begins to breakdown and the chromosomes begin to condense. Once the synaptonemal complex is gone, the homologous chromosomes remain attached to each various other at the centromere and at chiasmata. The chiasmata continue to be until anaphase I. The variety of chiasmata varies according come the varieties and the length of the chromosome. There must be at the very least one chiasma per chromosome for ideal separation the homologous chromosomes during meiosis I, yet there may be as numerous as 25. Following crossover, the synaptonemal facility breaks down and the cohesin connection between homologous bag is additionally removed. In ~ the end of prophase I, the pairs are hosted together only at the chiasmata (Figure 2) and are called tetrads due to the fact that the four sister chromatids of each pair that homologous chromosomes are now visible.


Figure 2. Crossover occurs between non-sister chromatids that homologous chromosomes. The result is an exchange of hereditary material between homologous chromosomes.


The crossover events are the very first source of hereditary variation in the nuclei created by meiosis. A single crossover event in between homologous non-sister chromatids leads to a mutual exchange of identical DNA in between a maternal chromosome and a head chromosome. Now, once that sister chromatid is moved into a gamete cabinet it will lug some DNA indigenous one parent of the individual and some DNA native the other parent. The sister recombinant chromatid has a mix of maternal and paternal genes that did no exist prior to the crossover. Lot of crossovers in an eight of the chromosome have actually the very same effect, exchanging segments the DNA to develop recombinant chromosomes.

Prometaphase I

The key event in prometaphase i is the attachments of the spindle fiber microtubules to the kinetochore protein at the centromeres. Kinetochore proteins space multiprotein complexes that bind the centromeres of a chromosome come the microtubules of the mitotic spindle. Microtubules prosper from centrosomes inserted at the contrary poles the the cell. The microtubules move toward the center of the cell and attach to among the 2 fused homologous chromosomes. The microtubules connect at each chromosomes’ kinetochores. Through each member of the homologous pair attached come opposite poles the the cell, in the next phase, the microtubules deserve to pull the homologous pair apart. A spindle fiber that has actually attached come a kinetochore is called a kinetochore microtubule. At the end of prometaphase I, every tetrad is attached come microtubules indigenous both poles, with one homologous chromosome facing each pole. The homologous chromosomes room still held together at chiasmata. In addition, the nuclear membrane has damaged down entirely.

Metaphase I

During metaphase I, the homologous chromosomes are arranged in the facility of the cell through the kinetochores dealing with opposite poles. The homologous pairs orient us randomly at the equator. Because that example, if the 2 homologous members the chromosome 1 room labeled a and also b, then the chromosomes might line up a-b, or b-a. This is essential in identify the genes carried by a gamete, together each will just receive among the two homologous chromosomes. Recall the homologous chromosomes are not identical. Lock contain slight distinctions in their hereditary information, bring about each gamete to have a unique genetic makeup.

This randomness is the physical basis because that the creation of the second form of hereditary variation in offspring. Think about that the homologous chromosomes the a sexually reproducing biology are initially inherited together two separate sets, one from every parent. Using humans as one example, one set of 23 chromosomes is present in the egg donated by the mother. The father offers the other collection of 23 chromosomes in the sperm that fertilizes the egg. Every cabinet of the multicell offspring has copies of the initial two to adjust of homologous chromosomes. In prophase ns of meiosis, the homologous chromosomes kind the tetrads. In metaphase I, these pairs line up at the midway point between the two poles that the cell to type the metaphase plate. Since there is an equal possibility that a microtubule fiber will encounter a maternally or paternally inherited chromosome, the arrangement of the tetrads in ~ the metaphase plate is random. Any kind of maternally inherited chromosome may confront either pole. Any kind of paternally inherited chromosome may likewise face either pole. The orientation of each tetrad is elevation of the orientation that the other 22 tetrads.

This event—the random (or independent) assortment that homologous chromosomes in ~ the metaphase plate—is the 2nd mechanism that introduces variation right into the gametes or spores. In each cell that undergoes meiosis, the arrangement of the tetrads is different. The variety of variations is dependence on the variety of chromosomes making up a set. There room two possibilities for orientation in ~ the metaphase plate; the possible variety of alignments thus equals 2n, wherein n is the number of chromosomes every set. Humans have 23 chromosome pairs, which outcomes in over eight million (223) feasible genetically-distinct gametes. This number does not include the variability the was previously developed in the sisters chromatids by crossover. Offered these 2 mechanisms, that is very unlikely that any kind of two haploid cell resulting native meiosis will have actually the same genetic composition (Figure 3).


Figure 3. Random, independent assortment during metaphase I deserve to be prove by considering a cell through a set of two chromosomes (n = 2). In this case, there space two possible arrangements at the equatorial airplane in metaphase I. The full possible number of different gametes is 2n, wherein n amounts to the variety of chromosomes in a set. In this example, there are four possible genetic combinations for the gametes. Through n = 23 in human cells, there are over 8 million possible combinations that paternal and also maternal chromosomes.


To summary the genetic results of meiosis I, the maternal and paternal genes are recombined by crossover events that occur between each homologous pair throughout prophase I. In addition, the arbitrarily assortment of tetrads on the metaphase key produces a unique mix of maternal and also paternal chromosomes that will make their way into the gametes.

Anaphase I

In anaphase I, the microtubules traction the connected chromosomes apart. The sister chromatids remain tightly bound together at the centromere. The chiasmata are damaged in anaphase I together the microtubules attached to the unify kinetochores pull the homologous chromosomes personally (Figure 4).


Figure 4. The procedure of chromosome alignment differs between meiosis I and meiosis II. In prometaphase I, microtubules connect to the fused kinetochores of homologous chromosomes, and the homologous chromosomes space arranged in ~ the midpoint the the cell in metaphase I. In anaphase I, the homologous chromosomes are separated. In prometaphase II, microtubules connect to the kinetochores the sister chromatids, and the sister chromatids space arranged at the midpoint that the cell in metaphase II. In anaphase II, the sister chromatids space separated.


Telophase I and Cytokinesis

In telophase, the be separated chromosomes come at the contrary poles. The remainder of the usual telophase events may or might not occur, depending on the species. In part organisms, the chromosomes decondense and also nuclear envelopes form around the chromatids in telophase I. In various other organisms, cytokinesis—the physics separation that the cytoplasmic contents into two daughter cells—occurs without reformation of the nuclei. In practically all types of animals and also some fungi, cytokinesis the end the cell components via a cleavage furrow (constriction of the actin ring the leads come cytoplasmic division). In plants, a cabinet plate is formed during cell cytokinesis through Golgi engine fusing at the metaphase plate. This cell plate will eventually lead come the formation of cell wall surfaces that different the two daughter cells.

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Two haploid cells are the end an outcome of the very first meiotic division. The cells room haploid due to the fact that at every pole, there is just one of each pair the the homologous chromosomes. Therefore, just one full collection of the chromosomes is present. This is why the cells are thought about haploid—there is just one chromosome set, even though each homolog still is composed of two sister chromatids. Recall that sister chromatids are just duplicates of among the two homologous chromosomes (except for alters that occurred during cross over). In meiosis II, these two sister chromatids will certainly separate, developing four haploid daughter cells.