Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

In a cross between two varieties of corn, \(g l_{1} g l_{1} W s_{3} W s_{3}(\) egg parent) \(\times G I_{1} G l_{1} w s_{3} w s_{3}\) (pollen parent), a triploid offspring was produced with the genetic constitution $G l_{1} G l_{1} g l_{1} W s_{3} w s_{3} w s_{3}\( From which parent, egg or pollen, did the \)2 n$ gamete originate? Is another explanation possible? Explain.

Short Answer

Expert verified
Answer: The \(2n\) gamete originated from the pollen parent. The alternative explanation, which is non-disjunction occurring in both parents simultaneously, is unlikely.

Step by step solution

01

Analyze the genetic makeup of the parents and the offspring

The egg parent has the genetic constitution: \(g l_{1} g l_{1} W s_{3} W s_{3}\). The pollen parent has the genetic constitution: \(G I_{1} G l_{1} w s_{3} w s_{3}\). The triploid offspring has the genetic constitution: \(G l_{1} G l_{1} g l_{1} W s_{3} w s_{3} w s_{3}\).
02

Compare genetic makeup of parents and offspring to determine origin of the \(2n\) gamete

From the genetic constitution of the offspring, we can see that it has two copies of \(G l_{1}\), one copy of \(g l_1\), three copies of \(W s_{3}\), and three copies of \(w s_{3}\). The genetic material from the egg parent cannot provide all of the genetic material needed to form the offspring, which means that it cannot be the source of \(2n\) gamete. This is because egg parent only has genes \(g l_{1}\) and \(W s_{3}\) in its genetic constitution. It has no copy of \(G l_{1}\) or \(w s_{3}\) in its genetic constitution. On the other hand, the genetic material from the pollen parent can provide two copies of \(G l_{1}\) and three copies of \(w s_{3}\), since it has both genes in its genetic constitution. Therefore, the \(2n\) gamete must have originated from the pollen parent.
03

Consider alternative explanations

The only alternative explanation could be an event called non-disjunction, which is the failure of homologous chromosomes or sister chromatids to separate properly during cell division. It can result in the incorrect distribution of genetic material, creating an abnormal number of chromosomes in offspring. However, the triploid offspring in this case has genetic material from both parents, so the non-disjunction during meiosis must have happened in both parents simultaneously. This scenario is unlikely, especially considering that the source of \(2n\) gamete was identified. Thus, the most plausible explanation is that the \(2n\) gamete originated from the pollen parent.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Drosophila may be monosomic for chromosome \(4,\) yet remain fer tile. Contrast the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) results of the following crosses involving the recessive chromosome 4 trait, bent bristles: (a) monosomic IV, bent bristles \(\times\) normal bristles; (b) monosomic \(\mathrm{IV}\), normal bristles \(\times\) bent bristles.

In a human genetic study, a family with five phenotypically normal children was investigated. Two children were "homozy. gous" for a Robertsonian translocation between chromosomes 19 and 20 (they contained two identical copies of the fused chromosome). They have only 44 chromosomes but a complete genetic complement. Three of the children were "heterozygous" for the translocation and contained 45 chromosomes, with one translocated chromosome plus a normal copy of both chromosomes 19 and \(20 .\) Two other pregnancies resulted in stillbirths. It was later discovered that the parents were first cousins. Based on this information, determine the chromosome compositions of the parents. What led to the stillbirths? Why was the discovery that the parents were first cousins a key piece of information in understanding the genetics of this family?

A boy with Klinefelter syndrome \((47, \mathrm{XXY})\) is born to a mother who is phenotypically normal and a father who has the X-linked skin condition called anhidrotic ectodermal dysplasia. The mother's skin is completely normal with no signs of the skin abnormality. In contrast, her son has patches of normal skin and patches of abnormal skin. (a) Which parent contributed the abnormal gamete? (b) Using the appropriate genetic terminology, describe the meiotic mistake that occurred. Be sure to indicate in which division the mistake occurred. (c) Using the appropriate genetic terminology, explain the son's skin phenotype.

Why do human monosomics most often fail to survive prenatal development?

Inversions are said to "suppress crossing over." Is this ter. minology technically correct? If not, restate the description accurately.

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free