CLE peptide

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CLE peptides (CLAVATA3/Embryo Surrounding Region-Related) are a group of peptides found in plants that are involved with cell signaling. Production is controlled by the CLE genes. Upon binding to a CLE peptide receptor in another cell, a chain reaction of events occurs, which can lead to various physiological and developmental processes. This signaling pathway is conserved in diverse land plants. [1]

Contents

Background

Plants and animals alike both use small polypeptides for signaling in cell-to-cell communication. CLAVATA3/Embryo Surrounding Region-Related, also known as a plant peptide hormone, signaling is important for cell to cell signaling but also long distance communication. These two actions are especially important for plant cells because they are stationary and must perform cell expansion. In multicellular organisms cell-to-cell communication has been found to be very crucial for many growth processes that occur inside the organism. The 12 or 13 amino acid polypeptides are the mature forms of the CLE proteins that are derived from the conserved CLE domains. [2] [3] [4] More and more CLE genes are being identified with more research being conducted in this area. CLE genes have not only been found in seed plants but also in lycophytes, bryophytes, and green algae. [5] [6]

Genes

Most research that has been conducted on CLE peptide signaling has been conducted with Arabidopsis , since this genome contains 32 members of the CLE gene family. CLV3 which belongs to the CLE family of genes is found within one or more tissues of Arabidopsis. All 32 members of the CLE family share two characteristics that include: encoding of a small protein with a putative secretion signal at their N- termini and contain a conserved CLE motif at or near their C-termini. [7] The 32 members of the CLE gene family originated from mutations of the original gene.

Structures

CLE peptides are coded by the CLE genes. These peptides vary in structure with each peptide structure performing a different job with in the plant. The minimal length of functioning CLE peptides has been found to be 12 amino acids with several critical residues. [8] There are two different peptide structures that are found within the plant and they are A-type and B-type. When A-type hormones are secreted the plant slows down the rate of root growth whereas the secretion of B-type peptides effects the vascular growth of the plant. [9] The secretion of A-type peptides speeds up the vascular development of the plant that is mediated by the B-type peptides. This suggests that these two types of peptides work together to regulate the growth of the plant. The specific peptides are: [8]

A-type peptides

B-type peptides

Signaling in the shoot apical meristem

Shoot apical meristems of Crassula ovata (left). Fourteen days later, leaves have developed (right). Apical Meristems in Crassula ovata.png
Shoot apical meristems of Crassula ovata (left). Fourteen days later, leaves have developed (right).
Tunica-Corpus model of the apical meristem (growing tip). The epidermal (L1) and subepidermal (L2) layers form the outer layers called the tunica. The inner L3 layer is called the corpus. Cells in the L1 and L2 layers divide in a sideways fashion, which keeps these layers distinct, whereas the L3 layer divides in a more random fashion. Meristeme couches.png
Tunica-Corpus model of the apical meristem (growing tip). The epidermal (L1) and subepidermal (L2) layers form the outer layers called the tunica. The inner L3 layer is called the corpus. Cells in the L1 and L2 layers divide in a sideways fashion, which keeps these layers distinct, whereas the L3 layer divides in a more random fashion.

Meristematic cells give rise to various organs of the plant and keep the plant growing. There are two types of meristematic tissues 1) Apical Meristem 2) Lateral Meristem. The Apical Meristem is of two types; the shoot apical meristem (SAM) gives rise to organs like the leaves and flowers, while the root apical meristem (RAM) provides the meristematic cells for the future root growth. SAM and RAM cells divide rapidly and are considered indeterminate, in that they do not possess any defined end status. In that sense, the meristematic cells are frequently compared to the stem cells in animals, which have an analogous behavior and function. Within plants SAM cells play a major role in the overall growth and development, this is due to the fact that all cells making up the major parts of the plant come from the shoot apical meristem (SAM). There are three different important area found within the SAM and they include the central zone, the peripheral zone), and the rib meristem. Each of these areas play an important in the production of new stem cells within the SAM. All SAMs are usually dome shaped and have structures that are layered and are described as the tunica and corpus. CLV3 plays an important role in regulating the production of stem cells within the Central Zone region of the (SAM), this is also true for the cell promoting WUSCHEL (WUS) gene. The combination of these two genes regulates stem cell production by WUS negatively or positively regulating the production of stem cells by controlling the CLV3 gene.; [10] [11]

Genes in other plants

CLE genes have been found in numerous monocots, dicots, and even moss. Research has even shown that some plants like rice contain the presence of a multi-CLE domain. [5] [7] Various CLE-like genes have also been found in the genomes of plant-parasitic nematodes such as beet, soybean and potato cyst nematodes. [12] [5] [13]

Related Research Articles

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In vascular plants, the roots are the organs of a plant that are modified to provide anchorage for the plant and take in water and nutrients into the plant body, which allows plants to grow taller and faster. They are most often below the surface of the soil, but roots can also be aerial or aerating, that is, growing up above the ground or especially above water.

<span class="mw-page-title-main">Vascular cambium</span> Main growth tissue in the stems, roots of plants

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<span class="mw-page-title-main">Meristem</span> Type of plant tissue involved in cell proliferation

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<span class="mw-page-title-main">Plant hormone</span> Chemical compounds that regulate plant growth and development

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<span class="mw-page-title-main">Auxin</span> Plant hormone

Auxins are a class of plant hormones with some morphogen-like characteristics. Auxins play a cardinal role in coordination of many growth and behavioral processes in plant life cycles and are essential for plant body development. The Dutch biologist Frits Warmolt Went first described auxins and their role in plant growth in the 1920s. Kenneth V. Thimann became the first to isolate one of these phytohormones and to determine its chemical structure as indole-3-acetic acid (IAA). Went and Thimann co-authored a book on plant hormones, Phytohormones, in 1937.

<span class="mw-page-title-main">Cytokinin</span> Class of plant hormones promoting cell division

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<span class="mw-page-title-main">Gravitropism</span> Plant growth in reaction to gravity and bending of leaves and roots

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<span class="mw-page-title-main">Lateral root</span> Plant root

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Ling Meng is a Chinese plant biologist in the Department of Plant and Microbial Biology at the University of California, Berkeley. She is currently a Postdoctoral Fellow at Lawrence Berkeley National Laboratory. She is best known for discovering a novel form of cellular communication in plants. Thioredoxin, while known to play an important role in biological processes such as cellular redox, is not fully understood in function. Meng's work at Berkeley has suggested that thioredoxin h9 is associated with the plasma membrane and is capable of moving from cell to cell through two important protein post-translation modifications: myristoylation and palmitoylation. She is the first to connect thioredoxin with the plasma membrane.

Lewis Jeffrey Feldman is a professor of plant biology at the University of California, Berkeley, Director of the University of California Botanical Garden and previously Associate Dean for Academic Affairs in the College of Natural Resources. He is in the Department of Plant and Microbial Biology. Feldman has taught at Berkeley since 1978. He received Berkeley's Distinguished Teaching Award in 1996. Feldman's research focuses on regulation of development in meristems/stem cells, root gravitropism, and redox regulation of plant development.

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<span class="mw-page-title-main">Micropeptide</span> Short length polypeptides

Micropeptides are polypeptides with a length of less than 100-150 amino acids that are encoded by short open reading frames (sORFs). In this respect, they differ from many other active small polypeptides, which are produced through the posttranslational cleavage of larger polypeptides. In terms of size, micropeptides are considerably shorter than "canonical" proteins, which have an average length of 330 and 449 amino acids in prokaryotes and eukaryotes, respectively. Micropeptides are sometimes named according to their genomic location. For example, the translated product of an upstream open reading frame (uORF) might be called a uORF-encoded peptide (uPEP). Micropeptides lack an N-terminal signaling sequences, suggesting that they are likely to be localized to the cytoplasm. However, some micropeptides have been found in other cell compartments, as indicated by the existence of transmembrane micropeptides. They are found in both prokaryotes and eukaryotes. The sORFs from which micropeptides are translated can be encoded in 5' UTRs, small genes, or polycistronic mRNAs. Some micropeptide-coding genes were originally mis-annotated as long non-coding RNAs (lncRNAs).

References

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Further reading