Concept explainers
To analyze:
Visual of human chromosome
Introduction:
Chromosome mapping is the arrangement of the chromosomes. Genetic mapping provides the clue about the position, structure and, location of the chromosomes.
To study the cytogenetics of chromosome; the G-banding or Giemsa banding technique is used. A karyotype is the arrangement and appearance of the chromosomes in the nucleus of the eukaryotic cell. Karyotyping specifically did to study the number of chromosomes, positions, banding pattern or differences between the sex chromosomes.
It is very challenging to figure out these aspects with simple staining procedures that applies uniform color to all structures or parts of the chromosome.
Hence, G-banding technique was developed that specifically highlights light and dark bands.
G-Banding is useful in the detection of genetic diseases through photographic visualizations of the entire chromosome.
In this technique- the metaphase chromosomes are partly digested and treated with trypsin, later stained with the Giemsa stain.
The dark bands refer to the rich A and T regions while light regions refer to the G and C rich regions.
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Genetic Analysis: An Integrated Approach (3rd Edition)
- Analyzing Karyotypes 1. Originally, karyotypic analysis relied only on size and centromere placement to identify chromosomes. Because many chromosomes are similar in size and centromere placement, the identification of individual chromosomes was difficult, and chromosomes were placed into eight groups, identified by the letters A to G. Today, each human chromosome can be readily identified. a. What technical advances led to this improvement in chromosome identification? b. List two ways this improvement can be implemented. c. What clinical information does a karyotype provide?arrow_forwardTabulate the different classifications. thank you. i really like your answers :)arrow_forwardDescribe two differences among these chromosomes.arrow_forward
- Suppose the banding pattern variation for chromosome 9 in sharks arose in the given order. The ancestral chromosome is numbered 7654321. Identify which chromosomal modifications are responsible for the banding pattern changes observed in each of the novel chromosomes. Thank you for your assistance and to show my appreciation an immediate like is guaranteed if answered correctly.arrow_forwardDiploid Number of chromosomes, Sex Chromosomes, (+/- whole) Chromosome (+/- partial) e.g. 47, XY, +14 = male with trisomy of chromosome 14 e.g. 46, XX, 1q+ = female with a partial increase to the length of the long arm of chromosome 1 (partial increases or decreases to a single chromosome still have the same diploid number) What is the notation for the following case A boy having Down syndromearrow_forwardWhy is chromosome 21 the smallest and not chromosome 22? considering that a karyogram is arranged from largest to smallestarrow_forward
- Diploid Number of chromosomes, Sex Chromosomes, (+/- whole) Chromosome (+/- partial) e.g. 47, XY, +14 = male with trisomy of chromosome 14 e.g. 46, XX, 1q+ = female with a partial increase to the length of the long arm of chromosome 1 (partial increases or decreases to a single chromosome still have the same diploid number) What is the notation for the following case? A man having Klinefelter syndrome and one Barr body.arrow_forwardSuppose the banding pattern variation for chromosome 9 in butterflies arose in the given order. The ancestral chromosome is numbered 7654321. Identify which chromosomal modifications are responsible for the banding pattern changes observed in each of the novel chromosomes.arrow_forwardDiploid Number of chromosomes, Sex Chromosomes, (+/- whole) Chromosome (+/- partial) e.g. 47, XY, +14 = male with trisomy of chromosome 14 e.g. 46, XX, 1q+ = female with a partial increase to the length of the long arm of chromosome 1 (partial increases or decreases to a single chromosome still have the same diploid number) What is the notation for the following cases? ( A female having Edwards syndrome (trisomy 18)arrow_forward
- Diploid Number of chromosomes, Sex Chromosomes, (+/- whole) Chromosome (+/- partial) e.g. 47, XY, +14 = male with trisomy of chromosome 14 e.g. 46, XX, 1q+ = female with a partial increase to the length of the long arm of chromosome 1 (partial increases or decreases to a single chromosome still have the same diploid number) What is the notation for the following cases? ( A male infant having cri du chat syndrome.arrow_forwardDiploid Number of chromosomes, Sex Chromosomes, (+/- whole) Chromosome (+/- partial) e.g. 47, XY, +14 = male with trisomy of chromosome 14 e.g. 46, XX, 1q+ = female with a partial increase to the length of the long arm of chromosome 1 (partial increases or decreases to a single chromosome still have the same diploid number) What is the notation for the following cases? ( A male having Patau syndrome (trisomy 13)arrow_forwardWith regard to the analysis of chromosome structure, explain theexperimental advantage that polytene chromosomes offer. Discusswhy changes in chromosome structure are more easily detected inpolytene chromosomes than in ordinary chromosomes.arrow_forward
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