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The XY sex-determination systemis a sex-determination systempresent in many mammals, including humans, some insects (Drosophila), some snakes, some fish (guppies), and some plants (Ginkgotree). In this system, the sexof an individual usually is determined by a pair of sex chromosomes. Typically, females have two of the same kind of sex ...
Human male XY chromosomes after G-banding. In humans, each cell nucleus contains 23 pairs of chromosomes, a total of 46 chromosomes. The first 22 pairs are called autosomes. Autosomes are homologous chromosomes i.e. chromosomes which contain the same genes (regions of DNA) in the same order along their chromosomal arms. The 23rd pair of ...
The accepted hypothesis of XY and ZW sex chromosome evolution in amniotes is that they evolved at the same time, in two different branches. [84] [85] No genes are shared between the avian ZW and mammal XY chromosomes [26] and the chicken Z chromosome is similar to the human autosomal chromosome 9, rather than X or Y.
The human Y chromosome showing the SRY gene which codes for a protein regulating sexual differentiation. Sexual differentiation in humans is the process of development of sex differences in humans. It is defined as the development of phenotypic structures consequent to the action of hormones produced following gonadal determination. [1]
If one of these atypical sperm cells contributes to the genetic makeup of a child, the child will have an extra Y-chromosome in each of the body's cells. [23] In some cases, the extra Y-chromosome results from nondisjunction during mitosis in early embryonic development. This can produce 46,XY/47,XYY mosaics. [23]
Sex-chromosome dosage compensation. Dosage compensation is the process by which organisms equalize the expression of genes between members of different biological sexes. Across species, different sexes are often characterized by different types and numbers of sex chromosomes. In order to neutralize the large difference in gene dosage produced ...
Chromosomal translocation. Chromosomal reciprocal translocation of the 4th and 20th chromosome. In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal, and Robertsonian translocation.
A Barr body (named after discoverer Murray Barr) [1] or X-chromatin is an inactive X chromosome. In species with XY sex-determination (including humans), females typically have two X chromosomes, [2] and one is rendered inactive in a process called lyonization. Errors in chromosome separation can also result in male and female individuals with ...