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IGCSE 生物 · 知识点 17

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两个棕色眼睛的父母可能生出蓝眼睛的孩子。这不是错误,一旦你能解读基因型,这也不足为奇。在本课结束时,你将……

英语旁白 · 英中内嵌字幕

17.1

染色体、基因与蛋白质

教学大纲
核心内容 补充内容
1 说明染色体由DNA组成,其中包含以基因为形式的遗传信息
2 将基因定义为编码蛋白质的DNA片段
3 将等位基因定义为基因的替代形式
4 结合X和Y染色体描述人类的性别遗传
5 说明基因中碱基的序列决定了用于合成特定蛋白质的氨基酸序列(不要求了解核苷酸结构的具体细节)
6 解释不同的氨基酸序列赋予蛋白质分子不同的形状
7 解释DNA通过控制包括酶、膜载体和神经递质受体在内的蛋白质生成来控制细胞功能
8 解释蛋白质的合成过程,仅限于: • 编码该蛋白质的基因保留在细胞核内 • 信使RNA (mRNA) 是基因的副本 • mRNA分子在细胞核内合成并移动到细胞质 • mRNA穿过核糖体 • 核糖体将氨基酸组装成蛋白质分子 • 特定的氨基酸序列由mRNA中的碱基序列决定(不要求了解转录或翻译的具体细节)
9 说明生物体内大多数体细胞含有相同的基因,但特定细胞中的许多基因不表达,因为细胞只制造其所需的特定蛋白质
10 描述单倍体细胞核为含有一套染色体的细胞核
11 描述二倍体细胞核为含有两套染色体的细胞核
12 说明在二倍体细胞中,每种类型的染色体都有一对,而在人类二倍体细胞中有23对

来源:Cambridge International 教学大纲

English
A model of the DNA double helix
DNA carries inherited information in its double-helix structure.

Chromosomes 染色体 are made of DNA, which carries the genetic information in units called genes 基因.

  • A gene is a length of DNA that codes 编码 for one protein 蛋白质.
  • An allele 等位基因 is an alternative form of a gene. For example, a gene for eye colour may have a brown allele and a blue allele.
A zoom-in: the nucleus holds chromosomes; one chromosome is an X-shape carrying a gene as a coloured band; the chromosome is made of DNA, a double helix
A chromosome is made of DNA and carries genes; a gene is a length of the DNA

Sex chromosomes

Sex is inherited through the sex chromosomes 性染色体. Females are XX and males are XY. An egg always carries an X; a sperm carries either an X or a Y, so the sperm decides the baby's sex. This gives a 1:1 ratio 比例 of girls to boys.

A Punnett square for sex: the mother's eggs both carry X, the father's sperm carry X or Y; the offspring are XX (girl) or XY (boy) in a 1 to 1 ratio
XX × XY gives a 1:1 ratio of girls to boys; the sperm decides the sex
词汇 训练
English 中文 拼音
chromosomes/ˈkrəʊməsəʊmz/ 染色体 rǎn sè tǐ
genes/dʒiːnz/ 基因 jī yīn
codes/kəʊdz/ 编码 biān mǎ
allele/əˈliːl/ 等位基因 děng wèi jī yīn
sex chromosomes/seks ˈkrəʊməsəʊmz/ 性染色体 xìng rǎn sè tǐ
ratio/ˈreɪʃɪəʊ/ 比例 bǐ lì
17.1

DNA 如何调控细胞(拓展)

English

The base sequence 碱基序列 of a gene sets the order of amino acids 氨基酸 in a protein. A different order of amino acids folds the protein into a different shape, and the shape decides its job. So DNA controls the cell by controlling which proteins are made — including enzymes 酶, membrane carriers and receptor proteins 受体蛋白 for neurotransmitters 神经递质.

Most body cells hold the same genes, but each cell only expresses 表达 (switches on) the genes it needs, so it makes only the proteins for its own job.

词汇 训练
English 中文 拼音
proteins/ˈprəʊtiːnz/ 蛋白质 dàn bái zhì
base sequence/beɪs ˈsiːkwəns/ 碱基序列 jiǎn jī xù liè
amino acids/əˈmiːnəʊ ˈæsɪdz/ 氨基酸 ān jī suān
enzymes/ˈenzaɪmz/ 酶 méi
receptor proteins/rɪˈseptə ˈprəʊtiːnz/ 受体蛋白 shòu tǐ dàn bái
neurotransmitters/ˈnjuːrətrænsmɪtəz/ 神经递质 shén jīng dì zhì
expresses/ekˈspresɪz/ 表达 biǎo dá
17.1

合成蛋白质(拓展)

English

In the eukaryotic cell model here, the gene stays in the nucleus 细胞核, but proteins are made in the cytoplasm 细胞质. The link between them is messenger 信使 RNA (mRNA):

  1. mRNA is made in the nucleus as a copy of the gene.
  2. the mRNA moves out into the cytoplasm and passes through a ribosome 核糖体.
  3. the ribosome reads the mRNA's bases 碱基 and joins amino acids in the matching order to build the protein.
Protein synthesis: in the nucleus, mRNA copies a gene and moves to the cytoplasm, where a ribosome reads it and joins amino acids into a protein
mRNA copies a gene, then a ribosome reads it to build a protein from amino acids
探索

从基因到蛋白质

沿 DNA 模板一步步走:每个碱基与一个 mRNA 碱基配对,每三个碱基(一个密码子)编码蛋白质中的一个氨基酸。

词汇 训练
English 中文 拼音
nucleus/ˈnjuːklɪəs/ 细胞核 xì bāo hé
cytoplasm/ˈsaɪtəplæzəm/ 细胞质 xì bāo zhì
messenger/ˈmesɪndʒə/ 信使 xìn shǐ
ribosome/ˈriːbəʊsəʊm/ 核糖体 hé táng tǐ
bases/ˈbeɪsɪz/ 碱基 jiǎn jī
17.2 17.3

有丝分裂

教学大纲
核心 补充
1 描述有丝分裂是一种核分裂过程,能产生遗传上完全相同的细胞(无需掌握有丝分裂各阶段的具体细节)
2 阐述有丝分裂在生物体生长、受损组织修复、细胞更新以及无性生殖中的作用
3 指出染色体在分裂期开始前会进行精确复制
4 说明在有丝分裂过程中,染色体的拷贝会发生分离,从而确保每个子细胞中的染色体数目保持不变
5 描述干细胞为未分化的细胞,它们通过有丝分裂产生子细胞,这些子细胞可进一步分化以执行特定功能
核心 补充
1 说明减数分裂参与配子的产生
2 描述减数分裂是一种染色体数目由二倍体减半为单倍体的减少分裂,从而产生遗传上不同的细胞(不要求掌握减数分裂各阶段的具体细节)

来源:Cambridge International 教学大纲

English
Mitosis: one cell into two
A human karyotype: chromosomes arranged in pairs
A karyotype shows the full set of chromosomes in a human cell.

Body cells are diploid 二倍体 (two sets of chromosomes; humans have 23 pairs). Gametes are haploid 单倍体 (one set). Cells make new cells by nuclear division 分裂, of two kinds.

Mitosis 有丝分裂:

  • makes two cells that are genetically identical to the parent cell.
  • the chromosomes are copied exactly (replication 复制) before division, so each daughter cell 子细胞 keeps the full chromosome number.
  • it is used for growth, repair of tissues, replacing old cells, and asexual reproduction 无性生殖.
  • stem cells 干细胞 are unspecialised cells that divide by mitosis; their daughter cells can then become specialised.

Meiosis 减数分裂:

  • makes gametes 配子.
  • it is a reduction division: the chromosome number is halved, from diploid to haploid.
  • the cells it makes are genetically different from one another.
Mitosis splits one cell into two identical diploid cells (for growth and repair); meiosis splits one cell into four different haploid gametes, each with one chromosome from each pair, in different combinations
Mitosis makes two identical diploid cells; meiosis makes four different haploid gametes
探索

有丝分裂

有丝分裂制造两个遗传上相同的细胞——用于生长、修复和无性生殖。

词汇 训练
English 中文 拼音
division/dɪˈvɪʒn/ 分裂 fēn liè
diploid/ˈdɪplɔɪd/ 二倍体 èr bèi tǐ
haploid/ˈhæplɔɪd/ 单倍体 dān bèi tǐ
mitosis/maɪˈtəʊsɪs/ 有丝分裂 yǒu sī fēn liè
replication/ˌreplɪˈkeɪʃn/ 复制 fù zhì
daughter cell/ˈdɔːtə sel/ 子细胞 zǐ xì bāo
asexual reproduction/eɪˈsekʃuːəl rɪprəˈdʌkʃn/ 无性生殖 wú xìng shēng zhí
stem cells/stem selz/ 干细胞 gàn xì bāo
meiosis/meɪˈəʊsɪs/ 减数分裂 jiǎn shù fēn liè
gametes/ˈɡæmiːts/ 配子 pèi zǐ
17.4

单基因遗传

教学大纲
核心 补充
1 描述遗传为遗传信息从一代向另一代的传递
2 描述基因型为生物体的遗传组成,并用其所含等位基因来表述
3 描述表型为生物体可观察到的特征
4 描述纯合子为具有某特定基因的两个相同等位基因的个体
5 指出两个相同的纯合子个体交配将是纯系(自交不分离)
6 描述杂合子为具有某特定基因的两个不同等位基因的个体
7 指出杂合子个体不会是纯系
8 描述显性等位基因为若存在于基因型中即会表达的等位基因
9 描述隐性等位基因为仅当基因型中不存在该基因的显性等位基因时才会表达的等位基因
10 解读系谱图以分析给定特征的遗传方式
11 使用遗传图解预测单基因杂交的结果并计算表型比例,仅限于 1:1 和 3:1 的比例 13 解释如何使用测交来确定未知基因型
12 在导致多种基因型的杂交中使用棋盘格法,推导并展示可能的不同基因型
14 描述共显性为杂合子生物中的两个等位基因均对表型有贡献的情况
15 解释 ABO 血型系统的遗传:表型包括 A、B、AB 和 O 型血,等位基因为 $I^A$、$I^B$ 和 $I^o$
16 描述伴性遗传特征为控制该性状的基因位于性染色体上,且该特征在一性别中出现频率高于另一性别
17 以红绿色盲为例说明伴性遗传
18 使用遗传图解预测涉及共显性或伴性遗传的单基因杂交结果并计算表型比例

来源:Cambridge International 教学大纲

English

Inheritance 遗传 is the passing of genetic information from one generation to the next. Learn these words:

Genotype to phenotype: BB and Bb give brown eyes; bb gives blue. B is dominant, b is recessive
A dominant allele shows with one copy; a recessive needs two
Word Meaning
genotype 基因型 the alleles an organism has (its genetic make-up)
phenotype 表现型 the features you can observe
dominant 显性 allele shown in the phenotype even if only one copy is present (written as a capital letter, e.g. B)
recessive 隐性 allele shown only when no dominant allele is present (small letter, e.g. b)
homozygous 纯合子 two identical alleles (BB or bb); these breed true, or pure-breeding 纯种
heterozygous 杂合子 two different alleles (Bb); not pure-breeding
探索

预测一次遗传杂交

一个庞纳特方格显示后代能从两个亲本继承的等位基因的可能组合。

词汇 训练
English 中文 拼音
inheritance/ɪnˈherɪtəns/ 遗传 yí chuán
genotype/ˈdʒenətaɪp/ 基因型 jī yīn xíng
phenotype/ˈfenətaɪp/ 表现型 biǎo xiàn xíng
dominant/ˈdɒmɪnənt/ 显性 xiǎn xìng
recessive/rɪˈsesɪv/ 隐性 yǐn xìng
homozygous/ˌhɒməˈzɪɡəs/ 纯合子 chún hé zǐ
pure-breeding/pjʊə ˈbriːdɪŋ/ 纯种 chún zhǒng
heterozygous/ˌhetrəˈzɪɡəs/ 杂合子 zá hé zǐ
17.4

单基因杂交

English

To predict the offspring of a cross 杂交 involving one gene, use a genetic diagram or a Punnett square 庞纳特方格:

  • write each parent's genotype, then the gametes (each gamete carries one allele).
  • combine them in a grid to find the possible offspring genotypes and phenotypes.

Two heterozygous parents (Bb × Bb) give a 3:1 ratio of dominant to recessive. A heterozygous crossed with a homozygous recessive (Bb × bb) gives a 1:1 ratio. You can also read a pedigree diagram 系谱图 (a family tree) to follow a feature and work out genotypes.

A Punnett square for Bb × Bb: the four offspring boxes are BB, Bb, Bb and bb, giving three with the dominant feature and one with the recessive feature — a 3 to 1 ratio
A Punnett square for Bb × Bb gives a 3:1 ratio of dominant to recessive

(Supplement) A test cross 测交 finds an unknown genotype: cross the unknown with a homozygous recessive. If any offspring show the recessive feature, the unknown must have been heterozygous.

Worked example. Brown eyes (B) are dominant to blue (b). Two brown-eyed parents have a blue-eyed child. Give the parents' genotypes, and the chance that their next child has blue eyes. Start from the child: blue is recessive, so the child must be bb, and it got one b from each parent. So each parent carries a b. But both parents show brown eyes, so each must also carry a B: both parents are Bb. The Punnett square for Bb × Bb gives BB, Bb, Bb and bb, so the chance of a blue-eyed child is 1 in 4 (25%). Always work backwards from the recessive individual - a recessive phenotype pins a genotype exactly, and the rest follows. The 25% applies to each child on its own: three brown-eyed children do not make the fourth blue.

探索

预测一次遗传杂交

一个庞纳特方格显示后代能从两个亲本继承的等位基因的可能组合。

探索

单因子杂交

设置每个亲本的基因型并读取子代结果。两个杂合子(Aa × Aa)产生3 : 1的比例。

词汇 训练
English 中文 拼音
cross/krɒs/ 杂交 zá jiāo
Punnett square/ˈpʌnɪt skweə/ 庞纳特方格 páng nà tè fāng gé
pedigree diagram/ˈpedɪɡriː ˈdaɪəɡræm/ 系谱图 xì pǔ tú
test cross/test krɒs/ 测交 cè jiāo
17.4

共显性与血型(拓展)

English

In codominance 共显性, both alleles in a heterozygous organism show in the phenotype.

The ABO blood groups 血型 are an example. The alleles are $I^A$, $I^B$ and $I^o$. The alleles $I^A$ and $I^B$ are codominant, while $I^o$ is recessive:

  • $I^A I^A$ or $I^A I^o$ → group A
  • $I^B I^B$ or $I^B I^o$ → group B
  • $I^A I^B$ → group AB (both alleles shown)
  • $I^o I^o$ → group O
探索

共显性杂交

当两个等位基因都在表型中显示(共显性)时,杂合子显示两个特征——用一个庞纳特方格算出来。

词汇 训练
English 中文 拼音
codominance/ˈkəʊdəmɪnəns/ 共显性 gòng xiǎn xìng
blood groups/blʌd ɡruːps/ 血型 xuè xíng
17.4

伴性遗传(拓展)

English

A sex-linked 伴性遗传 characteristic is controlled by a gene on a sex chromosome (usually the X). Because males have only one X chromosome, a recessive allele on it always shows in males, so the feature is more common in males than in females.

Red-green colour blindness 色盲 is an example: the recessive allele is on the X chromosome, so it is much more common in boys than in girls.

Common mistakes.

  • Mixing up gene and allele. A gene is the length of DNA for one protein (eye colour); an allele is one form of it (blue or brown).
  • Writing a Punnett square without the gametes. Show each parent's genotype, then the gametes (one allele each), then the offspring.
  • Reading a 3:1 ratio as a promise. It gives the chance for each child: a 1 in 4 chance of blue eyes does not mean exactly one child in four will have them.
  • Using different letters for the two alleles, such as B and r. Use the same letter for one gene: capital for dominant, small for recessive (B and b).
  • Thinking a dominant allele is more common or "stronger". Dominant only means it shows with one copy; a dominant allele can be rare.
  • Saying mitosis makes gametes. Mitosis makes identical diploid cells for growth and repair; meiosis makes the haploid gametes, which are all different.
  • Saying the mother decides a baby's sex. Every egg carries an X; the sperm carries X or Y, so it decides.
  • Calling group AB "a blend" of A and B. In codominance both alleles show fully in the phenotype: $I^A I^B$ is group AB, not something in between.
词汇 训练
English 中文 拼音
sex-linked/seks lɪŋkt/ 伴性遗传 bàn xìng yí chuán
colour blindness/ˈkʌlə ˈblaɪndnəs/ 色盲 sè máng
17.4

考试技巧

English
  • Gene = a length of DNA coding for a protein. Allele = one form of a gene.
  • Genotype = the alleles present; phenotype = what you see. Homozygous = two same; heterozygous = two different.
  • Dominant shows with one copy; recessive needs two copies.
  • Learn to draw a Punnett square. Bb × Bb → 3:1; Bb × bb → 1:1.
  • (Supplement) Codominance: both alleles show (blood group AB). Sex linkage: a gene on the X, more common in boys (colour blindness).

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