Genetic architecture of node-specific leaf length and candidate gene identification in maize revealed by a

Related Experiment Video

Updated: Nov 3, 2026

Experimental Design for Laser Microdissection RNA-Seq: Lessons from an Analysis of Maize Leaf Development
10:08

Experimental Design for Laser Microdissection RNA-Seq: Lessons from an Analysis of Maize Leaf Development

Published on: March 5, 2017

Haoran Lyu1,2, Fuyan Jiang2, Yuxiang Luo1,2

  • 1College of Agriculture, Yunnan University, Kunming, 650500, China.

BMC Plant Biology
|November 1, 2026
PubMed
Abstract

Keywords:
Candidate genesGWASLeaf lengthMaizeMulti-parent populationQTL mapping

More Related Videos

Improved Methods for Preparing Transverse Sections and Unrolled Whole Mounts of Maize Leaf Primordia for Fluorescence and Confocal Imaging06:11

Improved Methods for Preparing Transverse Sections and Unrolled Whole Mounts of Maize Leaf Primordia for Fluorescence and Confocal Imaging

Published on: September 22, 2023

In Situ Hybridization for the Precise Localization of Transcripts in Plants12:15

In Situ Hybridization for the Precise Localization of Transcripts in Plants

Published on: November 23, 2011

Related Concept Videos

Light Acquisition02:51

Light Acquisition

In order to produce glucose, plants need to capture sufficient light energy. Many modern plants have evolved leaves specialized for light acquisition. Leaves can be only millimeters in width or tens of meters wide, depending on the environment. Due to competition for sunlight, evolution has driven the development of increasingly larger leaves and taller plants, to avoid shading by their neighbors, along with the elaboration of root architecture and mechanisms to transport water and...
Monohybrid Crosses01:50

Monohybrid Crosses

In the 1850s and 1860s, Gregor Mendel investigated inheritance by performing monohybrid crosses in pea plants. He crossed two plants that were true-breeding for different traits. Based on his observations, Mendel proposed that organisms inherit two copies of each trait, one from each parent, and that dominant traits can hide recessive traits. These results formed the basis of two fundamental principles in genetics: the Principle of Uniformity and the Law of Segregation.Monohybrid Crosses Reveal...
Trihybrid Crosses02:27

Trihybrid Crosses

Trihybrid Crosses
Some of Mendel’s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A trihybrid cross is a combination of three individual monohybrid crosses. For example, plant height (tall vs. short), seed shape (round vs. wrinkled), and seed color (yellow vs. green).
The F1 generation plants of a trihybrid cross are heterozygous for all three traits and produce eight gametes. Upon self-fertilization, these gametes have an equal chance to...
Dihybrid Crosses01:22

Dihybrid Crosses

To determine whether traits are inherited together or separately, Gregor Mendel crossed pea plants that differed in two traits. These parental plants were homozygous for both traits but displayed different phenotypes. The first generation of offspring were all dihybrids, heterozygotes exhibiting the two dominant phenotypes. When self-fertilized, the dihybrids consistently produced progeny with a 9:3:3:1 ratio of four possible phenotype combinations. This ratio suggested that inheriting one...
Law of Independent Assortment02:36

Law of Independent Assortment

While Mendel’s Law of Segregation states that the two alleles for one gene are separated into different gametes, a different question of how different genes are inherited remains. For example, is the gene for tall plants inherited with the gene for green peas? Mendel asked this question by experimenting with a dihybrid cross; a cross in which both parents are homozygous for two distinct traits resulting in an F1 generation that are heterozygous for both traits.Let’s think of two homozygous...
Law of Segregation02:15

Law of Segregation

When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 generation, and could reappear in the next generation (F2). He concluded that one of the traits must be dominant over the other, thereby causing masking of one trait in the F1 generation. When he crossed the F1 plants, he found that 75% of the offspring in the F2 generation had the dominant phenotype, while 25% had the recessive phenotype.