heredity
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What is heredity?
Heredity, also known as inheritance or biological inheritance, is the process where particular characteristics are transmitted from parents to their offspring. It explains both the constancy of species and the variation within them, through genes, the functional units of heritable material found in all living cells.
The set of genes an offspring inherits is its genotype, while the phenotype is the organismâs outward appearance and development, shaped by interactions between genes and the environment. While the genotype remains constant, the phenotype changes with internal and external environmental factors. The degree to which traits are attributable to genes versus environment is a key focus in genetic studies.
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What are genes?
Genes are the functional units of heritable material found within all living cells. Every species member has a species-specific gene set that ensures the species' constancy. However, variations in gene form can occur among individuals within a species, providing the genetic basis for the fact that no two individuals (except identical twins) have exactly the same traits. Genes exert their effect mainly by determining the structure and function of the many thousands of different proteins, which in turn determine the characteristics of an organism.
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How are traits passed from parents to offspring?
Traits are passed from parents to offspring through heredity, the biological process where particular characteristics are transmitted from parents to their offspring. Every species member has a specific set of genes, ensuring the species' constancy. However, variations in gene forms among individuals cause different traits (except in identical twins).
Offspring inherit a gene set (genotype) from both parents, which is a mix of each parent's genetic material. An organism's outward appearance and the developmental outcome of its genes is its phenotype. The phenotype relies on complex interactions between genes and their environment, while the genotype remains constant during the organism's lifetime.
Genes reside in cellular structures called chromosomes, which replicate and are passed to daughter cells during mitosis. During meiosis, homologous pairs are organized, and one member is given to each gamete formed.
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What is DNA and what does it do in genetics?
DNA (deoxyribonucleic acid) is an organic chemical with a complex molecular structure found in all cells and many viruses. It encodes genetic information to transmit inherited traits.
DNA's structure is a double helix polymer, resembling a spiral staircase with two strands wound around each other. Each strand comprises monomer nucleotides, featuring a deoxyribose sugar molecule, a phosphate group, and one of four nitrogenous bases: adenine, guanine, cytosine, and thymine.
In genetics, DNA serves as the blueprint for heredity. A DNA segment that codes for a specific protein is called a gene. DNA replicates by separating into two single strands, each acting as a template for a new strand. This semiconservative replication ensures the stable inheritance of genetic traits.
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How do dominant and recessive genes affect the traits we have?
Alleles, which are different forms of a gene, influence our traits. A dominant allele will express its trait even when paired with a recessive allele in a heterozygous pairing. The combination of alleles that an organism carries is its genotype.
If the paired alleles are the same, the organismâs genotype is homozygous for that trait; if they are different, the organismâs genotype is heterozygous. However, in some cases, alleles can be codominant, where neither allele acts as dominant or recessive. Also, multiple genes may interact, with some masking the expression of others; these are called epistatic genes. All genetic traits result from the interactions of alleles.
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How can genetic mutations lead to changes in traits or inherited diseases?
Genetic mutations, which are changes in the DNA sequence of a gene, can lead to alterations in traits and inherited diseases. These mutations can range from small changes, such as a single nucleotide base substitution (point mutations), to large alterations involving multiple DNA bases.
Types of Mutations and Their Effects
- Point Mutations These include transitions and transversions. They can be silent (no change in the amino acid sequence), missense (resulting in a different amino acid), or nonsense (resulting in a premature stop codon and truncated protein).
- Frameshift Mutations These occur when there is an addition or deletion of DNA bases, which shifts the reading frame and alters all downstream codons. This typically results in a non-functional protein.
Impact of Mutations
Mutations in germ cells (gametes) can be passed on to offspring, causing inherited diseases. If a mutated gene is dominant, only one copy is needed for the disorder to manifest. If it is recessive, two copies are needed. Mutations can also affect protein function by altering the amino acid sequence, leading to enzyme inactivity or complete absence of the protein. Some mutations may cause uncontrolled cell division, leading to cancerous tumors.
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heredity, the sum of all biological processes by which particular characteristics are transmitted from parents to their offspring. The concept of heredity encompasses two seemingly paradoxical observations about organisms: the constancy of a species from generation to generation and the variation among individuals within a species. Constancy and variation are actually two sides of the same coin, as becomes clear in the study of genetics. Both aspects of heredity can be explained by genes, the functional units of heritable material that are found within all living cells. Every member of a species has a set of genes specific to that species. It is this set of genes that provides the constancy of the species. Among individuals within a species, however, variations can occur in the form each gene takes, providing the genetic basis for the fact that no two individuals (except identical twins) have exactly the same traits.
The set of genes that an offspring inherits from both parents, a combination of the genetic material of each, is called the organismâs genotype. The genotype is contrasted to the phenotype, which is the organismâs outward appearance and the developmental outcome of its genes. The phenotype includes an organismâs bodily structures, physiological processes, and behaviours. Although the genotype determines the broad limits of the features an organism can develop, the features that actually develop, i.e., the phenotype, depend on complex interactions between genes and their environment. The genotype remains constant throughout an organismâs lifetime; however, because the organismâs internal and external environments change continuously, so does its phenotype. In conducting genetic studies, it is crucial to discover the degree to which the observable trait is attributable to the pattern of genes in the cells and to what extent it arises from environmental influence.
Because genes are integral to the explanation of hereditary observations, genetics also can be defined as the study of genes. Discoveries into the nature of genes have shown that genes are important determinants of all aspects of an organismâs makeup. For this reason, most areas of biological research now have a genetic component, and the study of genetics has a position of central importance in biology. Genetic research also has demonstrated that virtually all organisms on this planet have similar genetic systems, with genes that are built on the same chemical principle and that function according to similar mechanisms. Although species differ in the sets of genes they contain, many similar genes are found across a wide range of species. For example, a large proportion of genes in bakerâs yeast are also present in humans. This similarity in genetic makeup between organisms that have such disparate phenotypes can be explained by the evolutionary relatedness of virtually all life-forms on Earth. This genetic unity has radically reshaped the understanding of the relationship between humans and all other organisms. Genetics also has had a profound impact on human affairs. Throughout history humans have created or improved many different medicines, foods, and textiles by subjecting plants, animals, and microbes to the ancient techniques of selective breeding and to the modern methods of recombinant DNA technology. In recent years medical researchers have begun to discover the role that genes play in disease. The significance of genetics only promises to become greater as the structure and function of more and more human genes are characterized.
This article begins by describing the classic Mendelian patterns of inheritance and also the physical basis of those patternsâi.e., the organization of genes into chromosomes. The functioning of genes at the molecular level is described, particularly the transcription of the basic genetic material, DNA, into RNA and the translation of RNA into amino acids, the primary components of proteins. Finally, the role of heredity in the evolution of species is discussed.
Basic features of heredity
Prescientific conceptions of heredity
Heredity was for a long time one of the most puzzling and mysterious phenomena of nature. This was so because the sex cells, which form the bridge across which heredity must pass between the generations, are usually invisible to the naked eye. Only after the invention of the microscope early in the 17th century and the subsequent discovery of the sex cells could the essentials of heredity be grasped. Before that time, ancient Greek philosopher and scientist Aristotle (4th century bc) speculated that the relative contributions of the female and the male parents were very unequal; the female was thought to supply what he called the âmatterâ and the male the âmotion.â The Institutes of Manu, composed in India between 100 and 300 ad, consider the role of the female like that of the field and of the male like that of the seed; new bodies are formed âby the united operation of the seed and the field.â In reality both parents transmit the heredity pattern equally, and, on average, children resemble their mothers as much as they do their fathers. Nevertheless, the female and male sex cells may be very different in size and structure; the mass of an egg cell is sometimes millions of times greater than that of a spermatozoon.
The ancient Babylonians knew that pollen from a male date palm tree must be applied to the pistils of a female tree to produce fruit. German botanist Rudolph Jacob Camerarius showed in 1694 that the same is true in corn (maize). Swedish botanist and explorer Carolus Linnaeus in 1760 and German botanist Josef Gottlieb Kölreuter, in a series of works published from 1761 to 1798, described crosses of varieties and species of plants. They found that these hybrids were, on the whole, intermediate between the parents, although in some characteristics they might be closer to one parent and in others closer to the other parent. Kölreuter compared the offspring of reciprocal crossesâi.e., of crosses of variety A functioning as a female to variety B as a male and the reverse, variety B as a female to A as a male. The hybrid progenies of these reciprocal crosses were usually alike, indicating that, contrary to the belief of Aristotle, the hereditary endowment of the progeny was derived equally from the female and the male parents. Many more experiments on plant hybrids were made in the 1800s. These investigations also revealed that hybrids were usually intermediate between the parents. They incidentally recorded most of the facts that later led Gregor Mendel (see below) to formulate his celebrated rules and to found the theory of the gene. Apparently, none of Mendelâs predecessors saw the significance of the data that were being accumulated. The general intermediacy of hybrids seemed to agree best with the belief that heredity was transmitted from parents to offspring by âblood,â and this belief was accepted by most 19th-century biologists, including English naturalist Charles Darwin.
The blood theory of heredity, if this notion can be dignified with such a name, is really a part of the folklore antedating scientific biology. It is implicit in such popular phrases as âhalf blood,â ânew blood,â and âblue blood.â It does not mean that heredity is actually transmitted through the red liquid in blood vessels; the essential point is the belief that a parent transmits to each child all its characteristics and that the hereditary endowment of a child is an alloy, a blend of the endowments of its parents, grandparents, and more-remote ancestors. This idea appeals to those who pride themselves on having a noble or remarkable âbloodâ line. It strikes a snag, however, when one observes that a child has some characteristics that are not present in either parent but are present in some other relatives or were present in more-remote ancestors. Even more often, one sees that brothers and sisters, though showing a family resemblance in some traits, are clearly different in others. How could the same parents transmit different âbloodsâ to each of their children?
Mendel disproved the blood theory. He showed (1) that heredity is transmitted through factors (now called genes) that do not blend but segregate, (2) that parents transmit only one-half of the genes they have to each child, and they transmit different sets of genes to different children, and (3) that, although brothers and sisters receive their heredities from the same parents, they do not receive the same heredities (an exception is identical twins). Mendel thus showed that, even if the eminence of some ancestor were entirely the reflection of his genes, it is quite likely that some of his descendants, especially the more remote ones, would not inherit these âgoodâ genes at all. In sexually reproducing organisms, humans included, every individual has a unique hereditary endowment.
Lamarckismâa school of thought named for the 19th-century pioneer French biologist and evolutionist Jean-Baptiste de Monet, chevalier de Lamarckâassumed that characters acquired during an individualâs life are inherited by his progeny, or, to put it in modern terms, that the modifications wrought by the environment in the phenotype are reflected in similar changes in the genotype. If this were so, the results of physical exercise would make exercise much easier or even dispensable in a personâs offspring. Not only Lamarck but also other 19th-century biologists, including Darwin, accepted the inheritance of acquired traits. It was questioned by German biologist August Weismann, whose famous experiments in the late 1890s on the amputation of tails in generations of mice showed that such modification resulted neither in disappearance nor even in shortening of the tails of the descendants. Weismann concluded that the hereditary endowment of the organism, which he called the germ plasm, is wholly separate and is protected against the influences emanating from the rest of the body, called the somatoplasm, or soma. The germ plasmâsomatoplasm are related to the genotypeâphenotype concepts, but they are not identical and should not be confused with them.
The noninheritance of acquired traits does not mean that the genes cannot be changed by environmental influences; X-rays and other mutagens certainly do change them, and the genotype of a population can be altered by selection. It simply means that what is acquired by parents in their physique and intellect is not inherited by their children. Related to these misconceptions are the beliefs in âprepotencyââi.e., that some individuals impress their heredities on their progenies more effectively than othersâand in âprenatal influencesâ or âmaternal impressionsââi.e., that the events experienced by a pregnant female are reflected in the constitution of the child to be born. How ancient these beliefs are is suggested in the Book of Genesis, in which Jacob produces spotted or striped progeny in sheep and goats by showing the flocks striped rods while the animals are breeding. Another such belief is âtelegony,â which goes back to Aristotle; it alleged that the heredity of an individual is influenced not only by his father but also by males with whom the female may have mated and who have caused previous pregnancies. Even Darwin, as late as 1868, seriously discussed an alleged case of telegony: that of a mare mated to a zebra and subsequently to an Arabian stallion, by whom the mare produced a foal with faint stripes on his legs. The simple explanation for this result is that such stripes occur naturally in some breeds of horses.
All these beliefs, from inheritance of acquired traits to telegony, must now be classed as superstitions. They do not stand up under experimental investigation and are incompatible with what is known about the mechanisms of heredity and about the remarkable and predictable properties of genetic materials. Nevertheless, some people still cling to these beliefs. Some animal breeders take telegony seriously and do not regard as purebred the individuals whose parents are admittedly âpureâ but whose mothers had mated with males of other breeds. Soviet biologist and agronomist Trofim Denisovich Lysenko was able for close to a quarter of a century, roughly between 1938 and 1963, to make his special brand of Lamarckism the official creed in the Soviet Union and to suppress most of the teaching and research in orthodox genetics. He and his partisans published hundreds of articles and books allegedly proving their contentions, which effectively deny the achievements of biology for at least the preceding century. The Lysenkoists were officially discredited in 1964.


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