Dihybrid Cross Practice Problems Answer Key

11 min read

Dihybrid Cross Practice Problems Answer Key

Dihybrid cross merupakan salah satu konsep dasar dalam genetika yang meninjau pewarisan dua sifat sekaligus. Pada artikel ini, kita akan mempelajari cara menyelesaikan soal latihan dihybrid cross, memahami pola pewarisan, dan melihat contoh jawaban lengkap. Dengan memahami langkah‑langkahnya, Anda bisa menguasai materi ini dan siap menghadapi ujian atau kuis.


Introduction

Dihybrid cross menggabungkan dua gen berbeda, biasanya dengan satu alel dominan dan satu alel resesif pada setiap gen. Contohnya: Punnett square untuk rasio 9:3:3:1 pada keturunan Musa (pisang) atau Pisum (kacang polong). Untuk memecahkan soal, kita harus:

  1. Menentukan genotipe induk (misalnya AaBb).
  2. Menentukan faktor genetik (kombinasi alel) pada setiap gamet.
  3. Membuat Punnett square 4×4 (karena 4 kombinasi gamet).
  4. Menghitung probabilitas setiap kombinasi fenotipik.

Berikut ini contoh soal lengkap beserta jawabannya.


Steps to Solve Dihybrid Cross Problems

Langkah Penjelasan Contoh
1. Tentukan genotipe induk Biasanya soal menyebutkan heterozigot pada kedua sifat (AaBb).
3. In practice, 75 % (r T), 6. Here's the thing — identifikasi sifat Tentukan dua sifat yang diteliti dan pola dominansi masing-masing. Hitung gamet** Kombinasi alel pada gamet: AT, At, aT, at.
**2. Think about it: Sifat A: warna bunga (merah = R dominan, putih = r resesif). Because of that,
4. Think about it: 25 % (R T), 18. Hitung persentase Gunakan rasio 9:3:3:1 untuk memudahkan. Practically speaking, 75 % (R t), 18. Sifat B: bentuk biji (konsentrat = T dominan, tidak konsentrat = t resesif).
**6. R T (merah & konsentrat) = 9/16; R t = 3/16; r T = 3/16; r t = 1/16. In real terms, buat Punnett square** Gunakan kotak 4×4 dan isi setiap sel dengan kombinasi gamet. Kelompokkan hasil**
**5. Even so, 16 kotak, setiap kotak berisi satu kombinasi genotipe keturunan. 25 % (r t).

Scientific Explanation

Dihybrid cross didasarkan pada Hukum Segregasi Mendel dan Hukum Independensi Gen. Hukum Segregasi menjelaskan bahwa setiap individu membawa dua alel untuk setiap sifat, dan alel tersebut memisah saat pembentukan gamet. Hukum Independensi mengamati bahwa alel untuk sifat berbeda segregasi secara independen, sehingga kombinasi alel pada gamet bersifat acak.

Misalnya, dalam Pisum sativum (kacang polong), sifat warna biji (B = kuning, b = hijau) dan kualitas biji (G = konsentrat, g = tidak konsentrat). Jika induk heterozigot untuk keduanya (BbGg), gamet yang terbentuk adalah:

  • BG
  • Bg
  • bG
  • bg

Setiap kombinasi ini memiliki probabilitas 1/4, sehingga Punnett square 4×4 menghasilkan 16 keturunan dengan proporsi 9:3:3:1 Which is the point..


Practice Problems

1. Classic Dihybrid Cross

Two pea plants, each heterozygous for seed color (Yy) and seed shape (Rr), are crossed. What is the probability that a seed from the F₂ generation will be yellow and round?

2. Fruit Fly Example

A fruit fly strain that is heterozygous for wing shape (Ww) and eye color (Ee) is crossed with another identical strain. Find the probability of obtaining a fly with normal wings and white eyes Not complicated — just consistent..

3. Plant Genetics

A tomato plant heterozygous for fruit size (S s) and fruit color (C c) is self‑pollinated. How many distinct phenotypes will appear in the F₂ generation, and what are their expected ratios?

4. Human Trait

A couple both heterozygous for cystic fibrosis (CF) and for a simple Mendelian trait of eye color (brown = B, blue = b). They have a child. What is the probability that the child will have blue eyes and be a carrier for cystic fibrosis?

5. Complex Cross

A plant with genotype AaBbCc × AaBbCc is crossed. List all possible genotypes of the offspring and calculate the probability of obtaining a plant that is homozygous dominant for all three traits (AA BB CC) Nothing fancy..


Answer Key

1. Classic Dihybrid Cross

  • Genotipe induk: YyRr × YyRr
  • Gametes: YR, Yr, yR, yr (1/4 each)
  • Punnett square (4×4) yields 16 combinations.
  • Yellow & round corresponds to YR combination.
  • Probability: ( \frac{9}{16} ) or 56.25 %.

2. Fruit Fly Example

  • Genotipe induk: WwEe × WwEe
  • Gametes: WE, We, wE, we
  • Normal wings & white eyes = W e combination.
  • Probability: ( \frac{3}{16} ) or 18.75 %.

3. Plant Genetics

  • F₂ phenotypes: 9 distinct combinations (3×3) but due to dominance we observe 4 phenotypes:
    1. Large & red (SR)
    2. Large & green (Sr)
    3. Small & red (sR)
    4. Small & green (sr)
  • Ratios: 9 : 3 : 3 : 1 (i.e., 9 large‑red, 3 large‑green, 3 small‑red, 1 small‑green).

4. Human Trait

  • Cystic fibrosis (CF): allele c is recessive, C is normal.
  • Eye color: B (brown) dominant, b (blue) recessive.
  • Child genotype possibilities:
    • For CF: 1/4 chance of cc (affected), 1/2 chance of Cc (carrier), 1/4 chance of CC (normal).
    • For eye color: 1/4 chance of bb (blue), 1/2 chance of Bb (brown), 1/4 chance of BB (brown).
  • Blue eyes & carrier for CF = bb and Cc.
  • Probability: ( \frac{1}{4} \times \frac{1}{2} = \frac{1}{8} ) or 12.5 %.

5. Complex Cross

  • Gametes per parent: 2^3 = 8 combinations (ABC, ABc, AbC, Abc, aBC, aBc, abC, abc).
  • Offspring genotypes: 8 × 8 = 64 possible genotypes.
  • Homozygous dominant (AA BB CC) requires both parents to contribute A, B, and C alleles.
  • Probability from each parent to contribute ABC = 1/8.
  • Combined probability: ( \frac{1}{8} \times \frac{1}{8} = \frac{1}{64} ) or 1.56 %.

FAQ

Q1: Why is the ratio 9:3:3:1 for dihybrid crosses?
A1: Because each of the two heterozygous traits segregates independently, giving 4 gametes per parent. The 4×4 Punnett square yields 16 possible genotypes. Counting phenotypes gives 9 with both dominant traits, 3 with one dominant and one recessive, another 3 with reverse, and 1 with both recessive.

Q2: Can dihybrid crosses involve more than two traits?
A2: Yes, but the complexity increases exponentially. For three traits, you need a 8×8 Punnett square (64 combinations). For more traits, computational tools are often used That's the part that actually makes a difference..

Q3: What if the traits are not completely independent?
A3: Linkage can reduce the likelihood of recombination between genes on the same chromosome, altering expected ratios. In such cases, map distances and recombination frequencies must be considered Worth keeping that in mind..

Q4: How do I handle incomplete dominance in a dihybrid cross?
A4: Treat each trait separately, noting that heterozygotes will exhibit a blended phenotype. Combine phenotypes across traits to obtain final ratios.

Q5: Are there shortcuts to avoid drawing a full Punnett square?
A5: Yes. Use probability multiplication: probability of a trait being dominant = 3/4, recessive = 1/4. Multiply probabilities for combined traits (e.g., dominant-dominant = (3/4)² = 9/16).


Conclusion

Mastering dihybrid cross practice problems equips you with a solid foundation in Mendelian genetics. By systematically identifying genotypes, generating gametes, constructing Punnett squares, and interpreting ratios, you can confidently solve complex genetic puzzles. Keep practicing with varied scenarios—human traits, plant breeding, or model organisms—and your understanding of inheritance will deepen, enabling you to tackle research questions and academic challenges alike.

6. Real‑World Application: Predicting Disease Risk in a Family

Consider a couple where one partner carries the cystic‑fibrosis allele (Cc) and the other is a carrier for sickle‑cell anemia (Ss). Both diseases are autosomal recessive and located on different chromosomes, so they assort independently. The couple also wishes to know the chance that a child will have both conditions.

Parent 1 (CF) Gametes Frequency
C (normal) C ½
c (mutant) c ½
Parent 2 (Sickle) Gametes Frequency
S (normal) S ½
s (mutant) s ½

Because the two loci are independent, each child receives one allele from each parent at each locus, creating a 4‑by‑4 theoretical Punnett matrix (16 possible genotype combos). Plus, the only genotype that yields both diseases is cc ss. The probability of receiving c from the first parent is ½, and the probability of receiving s from the second parent is also ½.

[ P(\text{cc ss}) = \frac{1}{2} \times \frac{1}{2} = \frac{1}{4} ]

But note that the child must also receive the recessive allele from the other parent at each locus, which is also ½ for each. Thus the full calculation is:

[ P(\text{cc ss}) = \frac{1}{2}\times\frac{1}{2}\times\frac{1}{2}\times\frac{1}{2}= \frac{1}{16}=6.25% ]

So there is a 6.25 % chance that a child will inherit both cystic fibrosis and sickle‑cell disease—a scenario that, while rare, underscores the importance of genetic counseling for couples with multiple carrier statuses.

7. Using Software Tools to Simplify Multi‑Trait Crosses

When the number of traits exceeds three, manual Punnett squares become unwieldy. Several free web‑based calculators and spreadsheet templates can generate genotype and phenotype frequencies in seconds:

Tool Features Best For
Mendelian Inheritance Calculator (MIT) – U of Washington Handles up to 5 loci, supports linkage maps, visualizes gamete frequencies. That's why Classroom demonstrations. On top of that,
Genotype Calculator (Bioinformatics. But org) Accepts custom dominance/recessive relationships, outputs both genotype and phenotype tables. Research projects with non‑standard dominance.
Excel “Punnett Square” Template Uses nested IF statements to auto‑populate a grid; can be expanded with VBA for >4 loci. Quick, offline calculations.

Learning to input parental genotypes and interpret the resulting tables is a valuable skill that saves time and reduces transcription errors, especially when you need to run multiple scenarios (e.Also, g. , testing the effect of a new allele or a linked marker) Worth knowing..

8. Common Pitfalls and How to Avoid Them

Pitfall Why It Happens Fix
Confusing genotype with phenotype Students often write “Bb” when they mean “brown eyes.Here's the thing — g. Practically speaking,
Miscalculating probabilities for multiple traits Multiplying the wrong fractions (e. females.
Forgetting that each parent contributes one allele per locus Over‑counting leads to inflated probabilities. On the flip side, g. In practice, , brown eyes = dominant phenotype).
Assuming independence when genes are linked Linked genes do not assort 50 % of the time. , using 3/4 for a recessive trait). Check chromosome maps; apply recombination frequency (e.In practice, g. ”
Neglecting sex‑linked inheritance X‑linked traits behave differently in males vs. And Remember the ½ rule: each gamete carries exactly one allele for each gene.

This is the bit that actually matters in practice.

9. Practice Problems for Mastery

  1. Tri‑hybrid cross: Two pea plants are heterozygous for seed shape (Rr), flower color (Pp), and plant height (Tt). What is the expected phenotypic ratio for round, purple, tall plants?
    Hint: Use the 3/4 probability for each dominant trait, then multiply.

  2. Linked genes: In fruit flies, the genes for eye color (white w, red +) and wing shape (vestigial vg, normal +) are 15 cM apart. A heterozygous female (w+ vg+) is crossed with a male homozygous recessive (ww vgvg). What proportion of offspring are expected to be white‑eyed, normal‑winged?

  3. Sex‑linked disorder: A carrier mother (XⁿXᴿ) for red‑green color blindness marries a normal‑vision father (XⁿY). List the genotypes and phenotypes of their children and calculate the probability of a son being color‑blind.

Working through these scenarios will reinforce the concepts covered and highlight where each rule—Mendelian segregation, independent assortment, linkage—applies.


Final Thoughts

Di‑hybrid (and multi‑trait) crosses are more than an academic exercise; they are the backbone of modern genetics, from predicting crop yields to assessing human disease risk. By:

  1. Identifying parental genotypes
  2. Enumerating all possible gametes
  3. Applying probability rules (multiplication for independent events, recombination fractions for linked genes)
  4. Interpreting the resulting ratios

you develop a systematic approach that works for any number of traits. The key is to stay organized—write out each step, double‑check allele frequencies, and, when the problem outgrows a paper‑pencil Punnett square, turn to reliable software tools.

With practice, the once‑daunting tables shrink to mental shortcuts, and you’ll be able to answer “What are the odds?Here's the thing — ” with confidence—whether you’re counseling a family, planning a breeding program, or simply solving a textbook problem. g.Keep experimenting, keep questioning the assumptions (e., independence, complete dominance), and you’ll find that the patterns of inheritance become a powerful lens through which to view the living world.

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