A chromosome is determined to be metacentric, acrocentric or telocentric by the location of its centromere. Centromeres are the point of attachment of two sister chromatids. Sister chromatids are formed during DNA replication prior to mitosis or meiosis. Chromosome Y by itself (when it is not replicating and there are no sister chromatids) is not acrocentric, as it wouldn't even have a centromere location.
A chromosome with a sub-terminal centromere has its centromere located towards one end of the chromosome rather than in the middle. This can affect the behavior of the chromosome during cell division and can impact genetic inheritance and variability.
Each chromosome has two arms, labeled p (the shorter of the two) and q (the longer). The p arm is named for "petite" meaning 'small'; the q arm is named q simply because it follows p in the alphabet. (According to the NCBI, "q" refers to the French word "queue".) They can be Metacentric A chromosome is metacentric if its two arms are roughly equal in length. In some cases, a metacentric chromosome is formed by balanced Robertsonian translocation: the fusion of two acrocentric chromosomes to form one metacentric chromosome. Submetacentric If arms' lengths are unequal, the chromosome is said to be submetacentric Acrocentric If the p (short) arm is so short that is hard to observe, but still present, then the chromosome is acrocentric (The "acro-" in acrocentric refers to the Greek word for "peak."). In an acrocentric chromosome the p arm contains genetic material including repeated sequences such as nucleolar organizing regions, and can be translocated without significant harm, as in a balanced Robertsonian translocation. The domestic horse genome includes one metacentric chromosome that is homologous to two acrocentric chromosomes in the conspecific but undomesticated Przewalski's horse. This may reflect either fixation of a balanced Robertsonian translocation in domestic horses or, conversely, fixation of the fission of one metacentric chromosome into two acrocentric chromosomes in Przewalski's horses. A similar situation exists between the human and great ape genomes; in this case, because more species are extant, it is apparent that the evolutionary sequence is a reduction of two acrocentric chromosomes in the great apes to one metacentric chromosome in humans Telocentric A telocentric chromosome's centromere is located at the terminal end of the chromosome. Telomeres may extend from both ends of the chromosome. For example, all mouse chromosomes are telocentric Holocentric With holocentric chromosomes, the entire length of the chromosome acts as the centromere. Examples of this type of centromere can be found scattered throughout the plant and animal kingdoms with the most well known example being in the worm, Caenorhabditis elegans.
The 17th human chromosome is known as chromosome 17. It is one of the 23 pairs of chromosomes in humans and contains around 1,200 genes. Chromosome 17 is associated with various genetic disorders and traits, including Smith-Magenis syndrome and hereditary breast and ovarian cancer.
That would be the chromosome number 23. Regarding the [sex] chromosome number 23, the female gametes always have a [haploid] X chromatid, whereas the male gametes are just as likely to possess a [haploid] X chromatid as they are to possess a [haploid] Y chromatid.
Y chromosome
Diploid chromosome number in standard laboratory mice (genus Mus) is 40: 19 autosomes and the X and Y sex chromosomes. Whereas the autosomes and the X Chromosome are telocentric (centromere at one end of the chromosome), the Y chromosome is acrocentric
An acrocentric is a chromosome which has the centomere, the central region, closer to one end than the other, thus having one short arm and one long arm.
A chromosome with a sub-terminal centromere has its centromere located towards one end of the chromosome rather than in the middle. This can affect the behavior of the chromosome during cell division and can impact genetic inheritance and variability.
I thought they were acrocentric (centromere positioned so close to the end of the chromosome that the short arm of the chromosome is not visible) rather than telocentric (centromere located completely at the terminal end of the chromosome).
Each chromosome has two arms, labeled p (the shorter of the two) and q (the longer). The p arm is named for "petite" meaning 'small'; the q arm is named q simply because it follows p in the alphabet. (According to the NCBI, "q" refers to the French word "queue".) They can be Metacentric A chromosome is metacentric if its two arms are roughly equal in length. In some cases, a metacentric chromosome is formed by balanced Robertsonian translocation: the fusion of two acrocentric chromosomes to form one metacentric chromosome. Submetacentric If arms' lengths are unequal, the chromosome is said to be submetacentric Acrocentric If the p (short) arm is so short that is hard to observe, but still present, then the chromosome is acrocentric (The "acro-" in acrocentric refers to the Greek word for "peak."). In an acrocentric chromosome the p arm contains genetic material including repeated sequences such as nucleolar organizing regions, and can be translocated without significant harm, as in a balanced Robertsonian translocation. The domestic horse genome includes one metacentric chromosome that is homologous to two acrocentric chromosomes in the conspecific but undomesticated Przewalski's horse. This may reflect either fixation of a balanced Robertsonian translocation in domestic horses or, conversely, fixation of the fission of one metacentric chromosome into two acrocentric chromosomes in Przewalski's horses. A similar situation exists between the human and great ape genomes; in this case, because more species are extant, it is apparent that the evolutionary sequence is a reduction of two acrocentric chromosomes in the great apes to one metacentric chromosome in humans Telocentric A telocentric chromosome's centromere is located at the terminal end of the chromosome. Telomeres may extend from both ends of the chromosome. For example, all mouse chromosomes are telocentric Holocentric With holocentric chromosomes, the entire length of the chromosome acts as the centromere. Examples of this type of centromere can be found scattered throughout the plant and animal kingdoms with the most well known example being in the worm, Caenorhabditis elegans.
The 17th human chromosome is known as chromosome 17. It is one of the 23 pairs of chromosomes in humans and contains around 1,200 genes. Chromosome 17 is associated with various genetic disorders and traits, including Smith-Magenis syndrome and hereditary breast and ovarian cancer.
No. An 'X' chromosome looks like an 'X'. The 'Y' chromosome looks like a deformed 'X'. It is noticeably different to an 'X' chromosome. Also, the 'Y' chromosome is only a third of the size of an 'X' chromosome - an 'X' chromosome is 155 million base pares, while the 'Y' chromosome is only 58 million base pairs.
An X chromosome is known as an X chromosome based on its shape, which resembles an X. The Y chromosome resembles a Y.
The Y chromosome is the male sex chromosome, but males also carry a X chromosome from their mother. XY. The female sex chromosome is the Y chromosome; YY is female. ( generally, as sex chromosome number in both sexes can vary )
The y-chromosome is only present in males. Men will a y-chromosome identical to that of their father, and his father, and his father, etc.
That would be the chromosome number 23. Regarding the [sex] chromosome number 23, the female gametes always have a [haploid] X chromatid, whereas the male gametes are just as likely to possess a [haploid] X chromatid as they are to possess a [haploid] Y chromatid.
One X chromosome and one Y chromosome, which determines male sex characteristics.