Just one.
Individuals with Turner syndrome typically have only one X chromosome, so they do not have Barr bodies present in their cells. Barr bodies are inactive X chromosomes that are typically found in cells with two X chromosomes.
The human cell is most likely from a female individual. Barr bodies are inactivated X chromosomes in females, and the absence of a Y chromosome indicates that the individual does not have male sex chromosomes.
BARR BODIES CAN BE SEEN AS A SMALL APPENDAGE ON THE NUCLEOUS OF A POLYMORPHONUCLEAR NEUTROPHIL OF BLOOD CELLS FROM A FEMALE HUMAN. THESE ARE ONE OF THE WHITE CELL TYPES SEEN ON A BLOOD SMEAR DONE ON A CBC. tim goodman clinical lab scientist
The individual likely has an intersex condition like Androgen Insensitivity Syndrome (AIS) where the body does not respond to androgens, and thus does not form Barr bodies in the nuclei. In AIS, the individual has XY chromosomes but develops female physical characteristics due to insensitivity to male hormones.
Barr bodies are important because they are condensed, inactive X chromosomes found in female cells, which helps balance gene expression between males and females. This process, called X chromosome inactivation, ensures dosage compensation between sexes and prevents overexpression of genes on the X chromosome in females. Barr bodies also play a role in regulating gene expression and maintaining cellular function.
Individuals with Turner syndrome typically have only one X chromosome, so they do not have Barr bodies present in their cells. Barr bodies are inactive X chromosomes that are typically found in cells with two X chromosomes.
if the extra Xwill be Barr bodies why dp kline felter males or Turnes female have certain problem
Barr bodies are inactivated X chromosomes found in females, and males typically do not have Barr bodies since they have one X and one Y chromosome. In the case of an individual with an extra Y chromosome (for example, XYY syndrome), there are no Barr bodies present, as Barr bodies are formed from X chromosomes only. Therefore, the presence of an extra Y chromosome does not contribute to Barr body formation.
The human cell is most likely from a female individual. Barr bodies are inactivated X chromosomes in females, and the absence of a Y chromosome indicates that the individual does not have male sex chromosomes.
BARR BODIES CAN BE SEEN AS A SMALL APPENDAGE ON THE NUCLEOUS OF A POLYMORPHONUCLEAR NEUTROPHIL OF BLOOD CELLS FROM A FEMALE HUMAN. THESE ARE ONE OF THE WHITE CELL TYPES SEEN ON A BLOOD SMEAR DONE ON A CBC. tim goodman clinical lab scientist
A Barr body is an inactivated X chromosome. An XXXY cell would contain 1 Barr Body. Men have no Barr bodies, and women have 1.
Yes, a female with Down syndrome has three copies of chromosome 21, but only two copies of the X chromosome. Regarding sex chromosomes, she is genetically normal. For this reason X chromosome inactivation would occur, and she would have one Barr body per cell.
A Barr body is the inactivated X chromosome that is usually found in the nuclei of female somatic cells. It can also occur in males when there is an abnormality and the male is XXY instead of the normal XY, a condition known as Klinefelter's syndrome. In this case, the male somatic cells would also contain a Barr body. --- The Barr body is the highly-condensed chromatin structure taken up by an inctivated X chromosome. The number of Barr bodies equal the number of inactive chromosomes.
Barr bodies are inactivated X chromosomes found in female mammals as a mechanism to equalize gene dosage between males (XY) and females (XX). In most human cells, only one X chromosome is active, while the other is condensed into a Barr body, typically occurring in somatic cells of females. In males, since there is only one X chromosome, Barr bodies are absent. Therefore, Barr bodies are primarily found in the cells of females, and not in most human cells overall, especially in male cells.
The individual likely has an intersex condition like Androgen Insensitivity Syndrome (AIS) where the body does not respond to androgens, and thus does not form Barr bodies in the nuclei. In AIS, the individual has XY chromosomes but develops female physical characteristics due to insensitivity to male hormones.
Barr bodies are important because they are condensed, inactive X chromosomes found in female cells, which helps balance gene expression between males and females. This process, called X chromosome inactivation, ensures dosage compensation between sexes and prevents overexpression of genes on the X chromosome in females. Barr bodies also play a role in regulating gene expression and maintaining cellular function.
A female with two Barr bodies typically has a combination of sex chromosomes indicating a condition like Turner syndrome (45,X) or a variant involving additional X chromosomes, such as Triple X syndrome (47,XXX). The presence of two Barr bodies suggests that she has three X chromosomes, as each additional X chromosome beyond one contributes one Barr body. This genetic configuration can lead to various developmental and physical characteristics, but many individuals with Triple X syndrome may be asymptomatic or have mild features.