Heredity
Heredity
We have seen that reproductive processes give rise to new individuals that are similar, but subtly different. We have discussed how some amount of variation is produced even during asexual reproduction. And the number of successful variations are maximised by the process of sexual reproduction. If we observe a field of sugarcane we find very little variations among the individual plants. But in a number of animals including human beings, which reproduce sexually, quite distinct variations are visible among different individuals. In this chapter, we shall be studying the mechanism by which variations are created and inherited.
8.1 ACCUMULATION OF VARIATION
DURING REPRODUCTION
Figure 8.1 Creation of diversity over succeeding generations. The original organism at the top will give rise to, say, two individuals, similar in body design, but with subtle differences. Each of them, in turn, will give rise to two individuals in the next generation. Each of the four individuals in the bottom row will be different from each other. While some of these differences will be unique, others will be inherited from their respective parents, who were different from each other.
$ \quad$ Inheritance from the previous generation provides both a common basic body design, and subtle changes in it, for the next generation. Now think about what would happen when this new generation, in its turn, reproduces. The second generation will have differences that they inherit from the first generation, as well as newly created differences (Fig. 8.1).
$ \quad$ Figure 8.1 would represent the situation if a single individual reproduces, as happens in asexual reproduction. If one bacterium divides, and then the resultant two bacteria divide again, the four individual bacteria generated would be very similar. There would be only very minor differences between them, generated due to small inaccuracies in DNA copying. However, if sexual reproduction is involved, even greater diversity will be generated, as we will see when we discuss the rules of inheritance.
$ \quad$ Do all these variations in a species have equal chances of surviving in the environment in which they find themselves? Obviously not. Depending on the nature of variations, different individuals would have different kinds of advantages. Bacteria that can withstand heat will survive better in a heat wave, as we have discussed earlier. Selection of variants by environmental factors forms the basis for evolutionary processes, as we will discuss in later sections.
QUESTIONS
1. If a trait A exists in $10 %$ of a population of an asexually reproducing species and a trait B exists in $60 %$ of the same population, which trait is likely to have arisen earlier?
Answer In asexual reproduction, the reproducing cells produce a copy of their DNA through some chemical reactions. However, this copying of DNA is not accurate and therefore, the newly formed DNA has some variations. It can be easily observed in the above figure that in asexual reproduction, very few variations are allowed. Therefore, if a trait is present in only $10 %$ of the population, it is more likely that the trait has arisen recently. Hence, it can be concluded that trait B that exists in $60 %$ of the same population has arisen earlier than trait A.Show Answer
Show Answer
Answer
Sometimes for a species, the environmental conditions change so drastically that their survival becomes difficult. For example, if the temperature of water increases suddenly, most of the bacteria living in that water would die. Only few variants resistant to heat would be able to survive. If these variants were not there, then the entire species of bacteria would have been destroyed. Thus, these variants help in the survival of the species.
However, not all variations are useful. Therefore, these are not necessarily beneficial for the individual organisms.
8.2 HEREDITY
The most obvious outcome of the reproductive process still remains the generation of individuals of similar design. The rules of heredity determine the process by which traits and characteristics are reliably inherited. Let us take a closer look at these rules.
8.2.1 Inherited Traits
What exactly do we mean by similarities and differences? We know that a child bears all the basic features of a human being. However, it does not look exactly like its parents, and human populations show a great deal of variation.
Activity 8.1
- Observe the ears of all the students in the class. Prepare a list of students having free or attached earlobes and calculate the percentage of students having each (Fig. 8.2). Find out about the earlobes of the parents of each student in the class. Correlate the earlobe type of each student with that of their parents. Based on this evidence, suggest a possible rule for the inheritance of earlobe types.
(a)
(b) Figure 8.2 (a) Free and (b) attached earlobes. The lowest part of the ear, called the earlobe, is closely attached to the side of the head in some of us, and not in others. Free and attached earlobes are two variants found in human populations.
8.2.2 Rules for the Inheritance of Traits Mendel’s Contributions
The rules for inheritance of such traits in human beings are related to the fact that both the father and the mother contribute practically equal amounts of genetic material to the child. This means that each trait can be influenced by both paternal and maternal DNA. Thus, for each trait there will be two versions in each child. What will, then, the trait seen in the child be? Mendel (see box) worked out the main rules of such inheritance, and it is interesting to look at some of his experiments from more than a century ago.
Gregor Johann Mendel (1822-1884)
Mendel was educated in a monastery and went on to study science and mathematics at the University of Vienna. Failure in the examinations for a teaching certificate did not suppress his zeal for scientific quest. He went back to his monastery and started growing peas. Many others had studied the inheritance of traits in peas and other organisms earlier, but Mendel blended his knowledge of science and mathematics and was the first one to keep count of individuals exhibiting a particular trait in each generation. This helped him to arrive at the laws of inheritance.
Mendel used a number of contrasting visible characters of garden peas - round/wrinkled seeds, tall/short plants, white/violet flowers and so on. He took pea plants with different characteristics - a tall plant and a short plant, produced progeny by crossing them, and calculated the percentages of tall or short progeny.
In the first place, there were no halfway characteristics in this firstgeneration, or $F 1$ progeny - no ‘medium-height’ plants. All plants were
F1
$F 1 \times F 1$
(Tt) $\quad(Tt)$
Figure 8.3
Inheritance of traits over two generations tall. This meant that only one of the parental traits was seen, not some mixture of the two. So the next question was, were the tall plants in the F1 generation exactly the same as the tall plants of the parent generation? Mendelian experiments test this by getting both the parental plants and these F1 tall plants to reproduce by self-pollination. The progeny of the parental plants are, of course, all tall. However, the second-generation, or F2, progeny of the F1 tall plants are not all tall. Instead, one quarter of them are short. This indicates that both the tallness and shortness traits were inherited in the F1 plants, but only the tallness trait was expressed. This led Mendel to propose that two copies of factor (now called genes) controlling traits are present in sexually reproducing organism. These two may be identical, or may be different, depending on the parentage. A pattern of inheritance can be worked out with this assumption, as shown in Fig. 8.3.
Activity 8.2
- In Fig. 8.3, what experiment would we do to confirm that the F2 generation did in fact have a 1:2:1 ratio of $TT$, $Tt$ and tt trait combinations?
In this explanation, both $TT$ and $Tt$ are tall plants, while only tt is a short plant. In other words, a single copy of ’ $T$ ’ is enough to make the plant tall, while both copies have to be ’ $t$ ’ for the plant to be short. Traits like ’ $T$ ’ are called dominant traits, while those that behave like ’ $t$ ’ are called recessive traits. Work out which trait would be considered dominant and which one recessive in Fig. 8.4.
What happens when pea plants showing two different characteristics, rather than just one, are bred with each other? What do the progeny of a tall plant with round seeds and a short plant with wrinkled-seeds look like? They are all tall and have round seeds. Tallness and round seeds are thus dominant traits. But what happens when these $F 1$ progeny are used to generate F2 progeny by self-pollination? A Mendelian experiment will find that some F2 progeny are tall plants with round seeds, and some were short plants with wrinkled seeds. However, there would also be some F2 progeny that showed new combinations. Some of them would be tall, but have wrinkled seeds, while others would be short, but have round seeds. You can see as to how new combinations of traits are formed in F2 offspring when factors controlling for seed shape and seed colour recombine to form zygote leading to form F2 offspring (Fig. 8.5). Thus, the tall/short trait and the round seed/wrinkled seed trait are independently inherited.
8.2.3 How do these Traits get Expressed?
How does the mechanism of heredity work? Cellular DNA is the information source for making proteins in the cell. A section of DNA that provides information for one protein is called the gene for that protein. How do proteins control the characteristics that we are discussing here? Let us take the example of tallness as a characteristic. We know that plants have hormones that can trigger growth. Plant height can thus depend on the amount of a particular plant hormone. The amount of the plant hormone made will depend on the efficiency of the process for making it. Consider now an enzyme that is important for this process. If this enzyme works efficiently, a lot of hormone will be made, and the plant will be tall. If the gene for that enzyme has an alteration that makes the enzyme less efficient, the amount of hormone will be less, and the plant will be short. Thus, genes control characteristics, or traits.
If the interpretations of Mendelian experiments we have been discussing are correct, then both parents must be contributing equally to the DNA of the progeny during sexual reproduction. We have disscussed this issue in the previous Chapter. If both parents can help determine the trait in the progeny, both parents must be contributing a copy of the same gene. This means that each pea plant must have two sets of all genes, one inherited from each parent. For this mechanism to work, each germ cell must have only one gene set.
How do germ-cells make a single set of genes from the normal two copies that all other cells in the body have? If progeny plants inherited a single whole gene set from each parent, then the experiment explained in Fig. 8.5 cannot work. This is because the two characteristics ’ $R$ ’ and ’ $y$ ’ would then be linked to each other and cannot be independently inherited. This is explained by the fact that each gene set is present, not as a single long thread of DNA, but as separate independent pieces, each called a chromosome. Thus, each cell will have two copies of each chromosome, one each from the male and female parents. Every germcell will take one chromosome from each pair and these may be of either maternal or paternal origin. When two germ cells combine, they will restore the normal number of chromosomes in the progeny, ensuring the stability of the DNA of the species. Such a mechanism of inheritance explains the results of the Mendel experiments, and is used by all sexually reproducing organisms. But asexually reproducing organisms also follow similar rules of inheritance. Can we work out how their inheritance might work?
8.2.4 Sex Determination
We have discussed the idea that the two sexes participating in sexual reproduction must be somewhat different from each other for a number
Figure 8.6
Sex determination in human beings of reasons. How is the sex of a newborn individual determined? Different species use very different strategies for this. Some rely entirely on environmental cues. Thus, in some animals like a few reptiles, the temperature at which fertilised eggs are kept determines whether the animals developing in the eggs will be male or female. In other animals, such as snails, individuals can change sex, indicating that sex is not genetically determined. However, in human beings, the sex of the individual is largely genetically determined. In other words, the genes inherited from our parents decide whether we will be boys or girls. But so far, we have assumed that similar gene sets are inherited from both parents. If that is the case, how can genetic inheritance determine sex?
The explanation lies in the fact that all human chromosomes are not paired. Most human chromosomes have a maternal and a paternal copy, and we have 22 such pairs. But one pair, called the sex chromosomes, is odd in not always being a perfect pair. Women have a perfect pair of sex chromosomes, both called X. But men have a mismatched pair in which one is a normal-sized X while the other is a short one called Y. So women are XX, while men are XY. Now, can we work out what the inheritance pattern of $X$ and $Y$ will be?
As Fig. 8.6 shows, half the children will be boys and half will be girls. All children will inherit an X chromosome from their mother regardless of whether they are boys or girls. Thus, the sex of the children will be determined by what they inherit from their father. A child who inherits an $X$ chromosome from her father will be a girl, and one who inherits a $Y$ chromosome from him will be a boy.
QUESTIONS
1. How do Mendel’s experiments show that traits may be dominant or recessive?
Answer Mendel selected true breeding tall (TT) and dwarf (tt) pea plants. Then, he crossed these two plants. The seeds formed after fertilization were grown and these plants that were formed represent the first filial or F1 generation. All the F1 plants obtained were tall.Show Answer
Answer Mendel crossed pea plants having round green seeds (RRyy) with pea plants having wrinkled yellow seeds (rrYY).Show Answer
Answer No. This information is not sufficient to determine which of the traits - blood group A or $O$ - is dominant. This is because we do not know about the blood group of all the progeny. Blood group A can be genotypically AA or AO. Hence, the information is incomplete to draw any such conclusion.Show Answer
Show Answer
Answer
In human beings, the females have two $X$ chromosomes and the males have one $X$ and one $Y$ chromosome. Therefore, the females are $XX$ and the males are $XY$.
The gametes, as we know, receive half of the chromosomes. The male gametes have 22 autosomes and either X or Y sex chromosome.
Type of male gametes: 22+X OR 22+ Y.
However, since the females have XX sex chromosomes, their gametes can only have $X$ sex chromosome.
Type of female gamete: 22+ X
Sex determination in humans
Thus, the mother provides only $X$ chromosomes. The sex of the baby is determined by the type of male gamete ( $X$ or $Y$ ) that fuses with the $X$ chromosome of the female.
What you have learnt
- Variations arising during the process of reproduction can be inherited.
- These variations may lead to increased survival of the individuals.
- Sexually reproducing individuals have two copies of genes for the same trait. If the copies are not identical, the trait that gets expressed is called the dominant trait and the other is called the recessive trait.
- Traits in one individual may be inherited separately, giving rise to new combinations of traits in the offspring of sexual reproduction.
- Sex is determined by different factors in various species. In human beings, the sex of the child depends on whether the paternal chromosome is $X$ (for girls) or $Y$ (for boys).
EXERCISSES
1. A Mendelian experiment consisted of breeding tall pea plants bearing violet flowers with short pea plants bearing white flowers. The progeny all bore violet flowers, but almost half of them were short. This suggests that the genetic make-up of the tall parent can be depicted as
(a) TTWW
(b) TTww
(c) TtWW
(d) $\quad TtWw$
Answer (c) The genetic make-up of the tall parent can be depicted as TtWW Since all the progeny bore violet flowers, it means that the tall plant having violet flowers has WW genotype for violet flower colour. Since the progeny is both tall and short, the parent plant was not a pure tall plant. Its genotype must be Tt. Therefore, the cross involved in the given question is $TtWw \times ttww$ $\downarrow$ $TtWw-ttww$ Therefore, half the progeny is tall, but all of them have violet flowers.Show Answer
Answer Let us assume that children with light-coloured eyes can either have LL or Ll or ll genotype. If the children have LL genotype, then their parents will also be of LL genotype. LL If the children with light-coloured eyes have $1 l$ genotype, then their parents will also have $1 l$ genotype. $11 \times l l$ $\downarrow$ ll Therefore, it cannot be concluded whether light eye colour is dominant or recessive.Show Answer
Answer Dogs have a variety of genes that govern coat colour. There are at least eleven identified gene series (A, B, C, D, E, F, G, M, P, S, T) that influence coat colour in dog. A dog inherits one gene from each of its parents. The dominant gene gets expressed in the phenotype. For example, in the B series, a dog can be genetically black or brown. Let us assume that one parent is homozygous black (BB), while the other parent is homozygous brown (bb) bb BB B B $bBbBb$ $bBbBb$ In this case, all the offsprings will be heterozygous (Bb). Since black (B) is dominant, all the offsprings will be black. However, they will have both B and $b$ alleles. If such heterozygous pups are crossed, they will produce 25% homozygous black (BB), $50 %$ heterozygous black ( $Bb$ ), and 25% homozygous brown (bb) offsprings. B b $BBBBb$ $bBbBb$Show Answer
Show Answer
Answer
In human beings, every somatic cell of the body contains 23 pairs of chromosomes. Out of these 23 pairs, the first 22 pairs are known as autosomes and the remaining one pair is known as sex chromosomes represented as $X$ and $Y$.
Females have two X chromosomes and males have one X and one Y chromosome.
The gamete receives half of the chromosomes. Therefore, the male gametes have 22 autosomes and either $X$ or $Y$ chromosome.
The female gamete, on the other hand, has 22 autosomes and X chromosome.
During reproduction, the male and female gametes fuse and thus the progeny receives 22 autosomes and one $X$ or $Y$ chromosome from male parent and 22 autosomes and one $X$ chromosome from the female parent.
Father 22 pairs of autosomes
XY
Mother
22 pairs of autosomes
Gamete
22 pairs of autosomes OR 22 pairs of autosomes
$+$
XY
