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Leber hereditary optic neuropathy|| Mitochondrial. C. Chapter 12 dna and rna answer key section review 12-1. DNA fingerprinting is a method for comparing the DNA sequences of any two individuals. As a result, it has one arm, which is extremely long and the other, which is extremely short. It is a result of replacement of GAG by GUG leading to the substitution of Glu by Val at sixth position of beta globin chain of haemoglobin. Page No 193: Question 1: a.
These solutions for Heredity And Variation are extremely popular among Class 9 students for Science Heredity And Variation Solutions come handy for quickly completing your homework and preparing for exams. Effect on blood-glucose level. • The ribose sugar and the phosphates form the backbone of a polynucleotide chain with nitrogenous bases linked to sugar moiety and projecting from the backbone. D. A RNA nucleotide has three main components − a nitrogenous base, a ribose sugar and a phosphate group. In order to prevent this transmission, people should get their blood examined before marriage to know if they are a carrier of any genetic disorder. A monohybrid cross is useful in determining the dominance of genes. • Two types of nitrogenous bases are present i. e. Chapter 12 dna and rna answer key 12-2. Purines (Adenine and Guanine) and Pyrimidines (Cytosine and Uracil). C. The component which is in the nuclei of cells and carries the hereditary characteristics is called chromosome. As a result, the chromosome has only one arm. A dihybrid cross is useful in studying the assortment of the offspring. C. |Monohybrid cross||Dihybrid cross|. It was the first discovered and described chromosomal disorder in humans. This mutation may be present on one or both the chromosomes. The applications of DNA fingerprinting are as follows: -.
The DNA molecule is made up of basic materials called nucleotides and each nucleotide is made up of three components: - Sugar. • The end of the chain which has a free phosphate moiety at 5'-end of ribose sugar is referred to as 5'-end and the other end of the chain having a free 3'-OH group at the ribose sugar is referred to as 3' -end of the polynucleotide chain. Genetic disorders are caused by changes in DNA sequences which can only be passed from one generation to another under specific circumstances. 44+X:Turner syndrome::44+XXY:-.............. This disorder arises during development. B. Monogenic disorders: Monogenic disorders are genetic disorders which are caused by a mutation in a single gene. Some of the examples of monogenic disorders are sickle cell anemia, cystic fibrosis, polycystic kidney etc. • Many nucleotides are linked through 3'-5' phosphodiester linkages to each other to form the polynucleotide chain. • A phosphate group is linked to 5'-OH of a nucleoside through phosphoester linkage to form a corresponding nucleotide. Chromosomes are divided into four types based on the position of the centromere. Chapter 11 dna and genes answer key. Question 7: Complete the tree diagram below based on types of hereditary disorders. B. DNA is a very large single molecule also called as macromolecule. If a carrier/sufferer of a genetic disorder marries a person who is also a carrier/ sufferer of the disorder, then there are chances that disorder will be passed on to the offsprings.
9% of the base sequences in all human beings are identical. Example- a cross between tall and dwarf plant||. DNA fingerprinting forms the basis of paternity testing since a child inherits polymorphism from both its parents. • A nitrogenous base is linked to the ribose sugar through N-glycosidic linkages to form a nucleoside (like adenosine, guanosine or cytidine and uridine). Klinefelter syndrome. There are 3 types of RNA: 3. rRNA (ribosomal RNA) − These are the work benches of translation. Down's Syndrome: Down's syndrome is caused due to the presence of an additional copy of chromosome 21 (Trisomy of 21).
It can be used for studying evolution and genetic diversity in a population. 44+XXY||Men are sterile|. Nitrogen bases are attached sugar from inwards that extends to join hydrogen bond and the complimentary nitrogenous base from other strand. The total number of chromosomes in people affected with Down's syndrome becomes 47. Rather, we sholud support and accept people with such disorders, so that they can live a normal life. It is the remaining 0.
1% that makes every individual unique. E. It is necessary for people to have their blood examined before marriage because the genetic disorders are transmitted only by reproduction. They play a structural and catalytic role during translation. Monogenic disorder||Effect on blood-glucose level|. There is no particular treatment for sickle cell anemia, the treatments which are available provide symptomatic relief from the symptoms associated with this disorder. Affected individual has short stature, small, round head, furrowed tongue, partially opened mouth, palm crease, congenital heart disease and mental retardation. Hereditary characters are transferred from parents to offsprings by gene, hence they are said to be structural and functional units of heredity.
All Science And Technology Solutions Solutions for class Class 9 Science are prepared by experts and are 100% accurate. A. Monohybrid cross is a cross between two parents that have one pair of contrasting characters; for example, if pea plant with yellow seed coat is crossed with pea plant having green seed coat then in the F1 generation all the plants produce yellow seeds. D. Chromosomes are mainly made up of DNA. The cross in which only two pairs of contrasting characters are involved is known as dihybrid cross. A. Chromosomes are thread-like structures found in the nucleus of all living cells. It has a double helix structure, similar to a ladder, which is twisted at both ends. Genetic disorders are not communicable diseases that would be transmitted to people who come in contact with people with genetic disoders.
44+XXY||Pale skin, white hairs|. E. Organisms produced through sexual reproduction show major variations. 3) Acrocentric chromosomes: In acrocentric chromosomes, the centromere is located close to the end of the chromosome. Explain Mendel's monohybrid progeny with the help of any one cross. Diabetes||Polygenic disorder||. View NCERT Solutions for all chapters of Class 9. 1) Metacentric chromosomes: In these chromosomes, the centromere is present in the middle, which gives rise to two equal arms.
Example- a cross between tall plant having red flower and a dwarf plant having white flower.