Animal chromosomes table. How many chromosomes do different animals have? Differences between males and females

Genetics is a science that studies the patterns of heredity and variability of all living beings. Exactly this science gives us knowledge about the number of chromosomes in different types organisms, the size of chromosomes, the location of genes on them, and how genes are inherited. Genetics also studies mutations that occur during the formation of new cells.

Chromosome set

Every living organism (the only exception is bacteria) has chromosomes. They are located in every cell of the body in a certain amount. In all somatic cells, chromosomes are repeated twice, thrice or large quantity times, depending on the type of animal or variety plant organism. In germ cells, the chromosome set is haploid, that is, single. This is necessary so that when two germ cells merge, the correct set of genes for the body is restored. However, the haploid set of chromosomes also contains genes responsible for the organization of the entire organism. Some of them may not appear in the offspring if the second reproductive cell contains more strong signs.

How many chromosomes does a cat have?

You will find the answer to this question in this section. Each type of organism, plant or animal, contains a specific set of chromosomes. The chromosomes of one type of creature have a certain length of the DNA molecule, a certain set of genes. Each such structure has its own size.

And dogs - our pets? A dog has 78 chromosomes. Knowing this number, is it possible to guess how many chromosomes a cat has? It's impossible to guess. Because there is no relationship between the number of chromosomes and the complexity of the organization of the animal. How many chromosomes does a cat have? There are 38 of them.

Chromosome size differences

A DNA molecule, with the same number of genes located on it, in different species can have different lengths.

Moreover, the chromosomes themselves have different size. One information structure can accommodate a long or very short DNA molecule. However, chromosomes are never too small. This is due to the fact that when daughter structures diverge, a certain weight of the substance is required, otherwise the divergence itself will not occur.

Number of chromosomes in different animals

As mentioned above, there is no relationship between the number of chromosomes and the complexity of the organization of the animal, because these structures have different sizes.

The number of chromosomes a cat has is the same number of other cats: tiger, jaguar, leopard, puma and other representatives of this family. Many canids have 78 chromosomes. Same amount domestic chicken. The domestic horse has 64, and the Przewalski's horse has 76.

Humans have 46 chromosomes. Gorillas and chimpanzees have 48, and macaques have 42.

The frog has 26 chromosomes. There are only 16 of them in the somatic cell of a pigeon. And in a hedgehog - 96. In a cow - 120. In a lamprey - 174.

Next, we present data on the number of chromosomes in the cells of some invertebrate animals. The ant, like the roundworm, has only 2 chromosomes in each somatic cell. A bee has 16 of them. A butterfly has 380 such structures in its cell, and radiolarians have about 1,600.

Animal data shows different quantities chromosomes. It should be added that Drosophila, which geneticists use during genetic experiments, has 8 chromosomes in somatic cells.

Number of chromosomes in different plants

Vegetable world is also extremely diverse in the number of these structures. Thus, peas and clover each have 14 chromosomes. Onion - 16. Birch - 84. Horsetail - 216, and fern - about 1200.

Differences between males and females

Males and females differ genetically in just one chromosome. In females this structure looks like the Russian letter “X”, and in males it looks like a “Y”. In some animal species, females have a “Y” chromosome and males have an “X”.

Traits located on such non-homologous chromosomes are inherited from father to son and from mother to daughter. The information that is fixed on the “Y” chromosome cannot pass on to the girl, because a person who has this structure is necessarily male.

The same applies to animals: if we see a calico cat, we can definitely say that this is a female.

Because only the X chromosome, which belongs to females, contains the corresponding gene. This structure is the 19th in the haploid set, that is, in germ cells, where the number of chromosomes is always two times less than in somatic ones.

The work of breeders

Knowing the structure of the apparatus that stores information about the body, as well as the laws of inheritance of genes and the characteristics of their manifestation, breeders develop new varieties of plants.

Wild wheat often has a diploid set of chromosomes. Not so much wild representatives, possessing a tetraploid set. Cultivated varieties more often contain tetraploid and even hexaploid sets of structures in their somatic cells. This improves yield, weather resistance, and grain quality.

Genetics is an interesting science. The structure of the apparatus, which contains information about the structure of the entire organism, is similar in all living beings. However, each type of creature has its own genetic characteristics. One of the characteristics of a species is the number of chromosomes. Organisms of the same species always have a certain constant number of them.

Poor ecology, life in constant stress, priority of career over family - all this has a bad effect on a person’s ability to bear healthy offspring. Sadly, about 1% of babies born with serious chromosome abnormalities grow up mentally or physically retarded. In 30% of newborns, deviations in the karyotype lead to the formation birth defects. Our article is devoted to the main issues of this topic.

The main carrier of hereditary information

As is known, a chromosome is a specific nucleoprotein (consisting of a stable complex of proteins and nucleic acids) structure inside the nucleus of a eukaryotic cell (that is, those living creatures whose cells have a nucleus). Its main function is the storage, transmission and implementation of genetic information. It is visible under a microscope only during processes such as meiosis (division of a double (diploid) set of chromosome genes during the creation of germ cells) and mycosis (cell division during the development of the organism).

As already mentioned, a chromosome consists of deoxyribonucleic acid (DNA) and proteins (about 63% of its mass) on which its thread is wound. Numerous studies in the field of cytogenetics (the science of chromosomes) have proven that DNA is the main carrier of heredity. It contains information that is subsequently implemented in a new organism. This is a complex of genes responsible for hair and eye color, height, number of fingers, etc. Which genes will be passed on to the child are determined at the time of conception.

Formation of the chromosome set of a healthy organism

U normal person 23 pairs of chromosomes, each of which is responsible for a specific gene. There are 46 in total (23x2) - how many chromosomes does healthy person. We get one chromosome from our father, the other is passed on from our mother. The exception is 23 pairs. It is responsible for the gender of a person: female is designated as XX, and male as XY. When the chromosomes are in a pair, this is a diploid set. In germ cells they are separated (haploid set) before being subsequently united during fertilization.

The set of characteristics of chromosomes (both quantitative and qualitative) examined within one cell is called a karyotype by scientists. Violations in it, depending on the nature and severity, lead to the occurrence of various diseases.

Deviations in the karyotype

When classified, all karyotype abnormalities are traditionally divided into two classes: genomic and chromosomal.

With genomic mutations, an increase in the number of the entire set of chromosomes, or the number of chromosomes in one of the pairs, is noted. The first case is called polyploidy, the second - aneuploidy.

Chromosomal abnormalities are rearrangements both within and between chromosomes. Without going into scientific jungle, they can be described as follows: some sections of chromosomes may not be present or may be doubled to the detriment of others; The sequence of genes may be disrupted, or their location may be changed. Disturbances in structure can occur in every human chromosome. Currently, the changes in each of them are described in detail.

Let us take a closer look at the most well-known and widespread genomic diseases.

Down syndrome

It was described back in 1866. For every 700 newborns, as a rule, there is one baby with a similar disease. The essence of the deviation is that a third chromosome is added to the 21st pair. This happens when the reproductive cell of one of the parents has 24 chromosomes (with double 21). The sick child ends up with 47 chromosomes – that’s how many chromosomes a Down person has. This pathology is promoted by viral infections or ionizing radiation suffered by parents, as well as diabetes.

Children with Down syndrome are mentally retarded. Manifestations of the disease are visible even in appearance: the tongue is too large, big ears irregular shape, skin fold on the eyelid and wide bridge of the nose, whitish spots in the eyes. Such people live on average forty years, because, among other things, they are susceptible to heart disease, problems with the intestines and stomach, and undeveloped genitals (although women may be capable of childbearing).

The older the parents, the higher the risk of having a sick child. Currently, there are technologies that make it possible to recognize chromosomal abnormalities in early stage pregnancy. Older couples need to undergo a similar test. It will not hurt young parents if one of them has had Down syndrome in their family. The mosaic form of the disease (the karyotype of some cells is damaged) is formed already at the embryonic stage and does not depend on the age of the parents.

Patau syndrome

This disorder is trisomy of the thirteenth chromosome. It occurs much less frequently than the previous syndrome we described (1 in 6000). It occurs when an extra chromosome is attached, as well as when the structure of chromosomes is disrupted and their parts are redistributed.

Patau syndrome is diagnosed by three symptoms: microphthalmos (reduced eye size), polydactyly (more fingers), cleft lip and palate.

The infant mortality rate for this disease is about 70%. Most of them do not live to be 3 years old. Individuals susceptible to this syndrome most often have heart and/or brain defects, problems with other internal organs(kidneys, spleen, etc.).

Edwards syndrome

Most babies with 3 eighteenth chromosomes die soon after birth. They have pronounced malnutrition (digestive problems that prevent the child from gaining weight). The eyes are set wide and the ears are low. Heart defects are often observed.

conclusions

To prevent the birth of a sick child, it is advisable to undergo special examinations. IN mandatory the test is indicated for women giving birth after 35 years; parents whose relatives were exposed to similar diseases; patients with thyroid problems; women who have had miscarriages.

Real hedgehogs. Small and medium-sized mammals. Body length is 13-27 cm. Tail length is 1-5 cm. The dorsal surface of the body is covered with spines that extend onto the sides. Between the needles there are thin, long, very sparse hairs.

On the ventral side of the body, the spines are absent and replaced by long and coarse hair. The head is relatively large, wedge-shaped, with a slightly elongated facial region. The ears are wide and rounded at the base. Their length never exceeds half the length of the head. Coloring The dorsal side of the body is very variable: chocolate brown or almost black, sometimes almost white. The ventral surface is usually brownish or grayish. The skull is somewhat flattened in the dorsoventral direction, with an expanded braincase, widely spaced strong zygomatic arches and a shortened rostral part, which has a fairly significant width. The bony auditory tympani are small in size and flattened. Dental formula: I 3/2 C 1/2 P 3/2 M 3/3 = 36.
U common hedgehog diploid chromosome number 48.

Inhabitants various landscapes. Avoid heavily swampy areas and continuous tracts of tall forests. They prefer forest edges, clearings, and bush thickets. Found in forest-steppe and steppe. Activity is predominantly crepuscular and nocturnal. For the winter, the common hedgehog makes a ground nest, collecting dry grass and leaves in a heap. The nest is located under heaps of dead wood, under the roots of trees. In October - November it goes into hibernation, lasting until warm weather. spring days.

By nature of nutrition omnivorous. They eat various invertebrate and vertebrate animals (mouse-like rodents, lizards, frogs, various insects, their larvae), as well as some plant objects (fruits). Mating for the common hedgehog in the northern part of its range occurs in the spring, shortly after awakening from hibernation. In the tropics, no seasonality in reproduction was observed among representatives of the genus. The common hedgehog has one litter per year.

Pregnancy approximately 5-6 weeks. The female gives birth to 3 to 8 cubs (usually about 4). Newborns of the common hedgehog weigh on average 12 g and have clearly visible spines in the head area. By 15 days, their spiny cover is already well defined. The eyes open on the 14th to 18th day after birth. Sexual maturity occurs in the 2nd year of life. Lifespan approximately 6 years.

Spreading covers Europe, Central Asia, Northern and Northeastern China, the Korean Peninsula and Africa from Morocco and Libya to Angola. The common hedgehog is acclimatized to New Zealand.

The taxonomy of the genus has not been definitively established; 5 species are usually distinguished.

Our country is inhabited by: the common hedgehog (from the northern shores of Lake Ladoga south to the Crimea and the Caucasus inclusive, in western regions northern Kazakhstan, V Western Siberia, in the southern part Amur region and Primorsky Krai) and

Did Charles Darwin renounce his theory of human evolution at the end of his life? Did ancient people find dinosaurs? Is it true that Russia is the cradle of humanity, and who is the yeti - perhaps one of our ancestors, lost through the centuries? Although paleoanthropology - the science of human evolution - is booming, the origins of man are still surrounded by many myths. These are anti-evolutionist theories and legends generated by popular culture, and pseudo-scientific ideas that exist among educated and well-read people. Do you want to know how everything “really” was? Alexander Sokolov, Chief Editor portal ANTHROPOGENES.RU, collected a whole collection of similar myths and checked how valid they are.

At the level of everyday logic, it is obvious that “a monkey is cooler than a person - it has two more chromosomes!” Thus, “the origin of man from the ape is finally refuted”...

Let us remind our dear readers that chromosomes are the things in which DNA is packaged in our cells. Humans have 23 pairs of chromosomes (23 we got from our mom and 23 from our dad. Total is 46). Full set chromosomes is called a "karyotype". Each chromosome contains a very large DNA molecule, tightly coiled.

It is not the number of chromosomes that is important, but the genes that these chromosomes contain. The same set of genes can be packaged into different numbers of chromosomes.

For example, two chromosomes were taken and merged into one. The number of chromosomes has decreased, but the genetic sequence they contain remains the same. (Imagine that a wall was broken between two adjacent rooms. The result is one large room, but the contents - furniture and parquet flooring - are the same...)

The fusion of chromosomes occurred in our ancestor. This is why we have two fewer chromosomes than chimpanzees, despite the fact that the genes are almost the same.

How do we know about the similarity of human and chimpanzee genes?

In the 1970s, when biologists learned to compare the genetic sequences of different species, they did this for humans and chimpanzees. The specialists were in for a shock: “ The difference in the nucleotide sequences of the substance of heredity - DNA - in humans and chimpanzees as a whole amounted to 1.1%,– wrote the famous Soviet primatologist E.P. Friedman in the book “Primates”. -... Species of frogs or squirrels within the same genus differ from each other 20–30 times more than chimpanzees and humans. This was so surprising that it was urgently necessary to somehow explain the discrepancy between the molecular data and what is known at the level of the whole organism» .

And in 1980, in a reputable magazine Science An article by a team of geneticists at the University of Minneapolis was published: The Striking Resemblance of High-Resolution G-Banded Chromosomes of Man and Chimpanzee (“Striking similarity of high-resolution stained chromosomes of humans and chimpanzees”).

The researchers used the latest methods of chromosome coloring at that time (transverse stripes appear on the chromosomes different thicknesses and brightness; Moreover, each chromosome is distinguished by its own special set of stripes). It turned out that in humans and chimpanzees the chromosome striations are almost identical! But what about the extra chromosome? It’s very simple: if, opposite the second human chromosome, we put the 12th and 13th chimpanzee chromosomes in one line, connecting them at their ends, we will see that together they make up the second human chromosome.

Later, in 1991, researchers took a closer look at the point of the putative fusion on the second human chromosome and found there what they were looking for - DNA sequences characteristic of telomeres - the end sections of chromosomes. Another proof that in place of this chromosome there were once two!

But how does such a merger happen? Let's say that one of our ancestors had two chromosomes combined into one. He ended up with an odd number of chromosomes - 47, while the rest of the non-mutated individuals still had 48! And how did such a mutant then reproduce? How can individuals with different numbers of chromosomes interbreed?

It would seem that the number of chromosomes clearly distinguishes species from each other and is an insurmountable obstacle to hybridization. Imagine the surprise of the researchers when, while studying the karyotypes of various mammals, they began to discover variations in the number of chromosomes within some species! So, in different populations common shrew this figure can range from 20 to 33. And the varieties of the musk shrew, as noted in the article by P. M. Borodin, M. B. Rogacheva and S. I. Oda, “differ from each other more than humans from chimpanzees: animals living in the south of Hindustan and Sri Lanka , have 15 pairs of chromosomes in their karyotype, and all other shrews from Arabia to the islands of Oceania have 20 pairs... It turned out that the number of chromosomes decreased because five pairs of chromosomes of a typical variety merged with each other: 8th with 16th, 9? I’m from 13th, etc.”

Mystery! Let me remind you that during meiosis - cell division, which results in the formation of sex cells - each chromosome in the cell must connect with its homologue pair. And then, when fused, an unpaired chromosome appears! Where should she go?

It turns out that the problem is solved! P. M. Borodin describes this process, which he personally recorded in 29-chromosomal punares. Punare are bristly rats native to Brazil. Individuals with 29 chromosomes were obtained by crossing between 30- and 28-chromosomal punares belonging to different populations this rodent.

During meiosis in such hybrids, paired chromosomes successfully found each other. “And the remaining three chromosomes formed a triple: on the one hand, a long chromosome received from the 28-chromosomal parent, and on the other, two shorter ones, which came from the 30-chromosomal parent. At the same time, each chromosome fell into place"