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Zhang, H. Regulators of Starch Biosynthesis in Cereal Crops. Encyclopedia. Available online: https://encyclopedia.pub/entry/16877 (accessed on 18 November 2024).
Zhang H. Regulators of Starch Biosynthesis in Cereal Crops. Encyclopedia. Available at: https://encyclopedia.pub/entry/16877. Accessed November 18, 2024.
Zhang, Huali. "Regulators of Starch Biosynthesis in Cereal Crops" Encyclopedia, https://encyclopedia.pub/entry/16877 (accessed November 18, 2024).
Zhang, H. (2021, December 08). Regulators of Starch Biosynthesis in Cereal Crops. In Encyclopedia. https://encyclopedia.pub/entry/16877
Zhang, Huali. "Regulators of Starch Biosynthesis in Cereal Crops." Encyclopedia. Web. 08 December, 2021.
Regulators of Starch Biosynthesis in Cereal Crops
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This entry is adapted from the peer-reviewed paper 10.3390/molecules26237092

Starch is the main food source for human beings and livestock all over the world, and it is also the raw material for production of industrial alcohol and biofuel. Because of the complexity and flexibility of carbon allocation in the formation of endosperm starch, cereal crops require a broad range of enzymes and one matching network of regulators to control the providential functioning of these starch biosynthetic enzymes.

starch biosynthesis cereal crops transcription factors

1. Introduction

As a fundamental commodity, starch was and is still widely used for human consumption in food and non-food industries [1][2]. Since starch is the major storage carbohydrate and generally accumulated in the heterotrophic starch-storing organs of crops [3][4][5], a large amount of starch is sourced from the attainable parts of staple crop plants [5], especially for cereal seeds, roots, and tubers. Among them, cereal seeds make up most of the worldwide annual starch production.

Starch is composed of amylose and amylopectin glucan polymers, which are packaged to form the insoluble semi-crystalline starch granules [6]. Starch synthesized in cereal crops contains at least two types, termed transitory starch and storage starch. Transitory starch is usually found in the plastid of photosynthetic organs and displays circadian turnover regulation with diurnal cycles [7]. While the storage starch is synthesized in the amyloplasts of non-photosynthetic sink tissues (i.e., seed endosperm), and requires the supply of sucrose and ATP from the source organs (i.e., leaves) [5]. Interestingly, some common regulatory factors of starch synthesis exist between chloroplasts and amyloplasts. For example, the expression of starch biosynthetic genes, i.e., GBSSI , was partly mediated by tetrapyrrole intermediates, i.e., heme, in endosperm during early seed development in rice [8], suggesting potential shared regulatory networks in various plastids.

The process of starch biosynthesis in crops requires tight cooperation of various starch biosynthetic enzymes, and coordinates with other metabolisms. Until now, a great number of genes involved in starch biosynthesis have been identified in various cereals. However, despite these findings, the regulatory factors underlying starch synthesis are still poorly understood, especially regarding the regulation of starch biosynthetic genes. Therefore, the screening and identification of key regulators is vital to understanding the fundamental regulatory mechanism underlying starch synthesis.

2. Transcription Factors Directly Regulating Starch Biosynthesis

Interestingly, ZmbZIP91 [9] and O2 [10] are the two closest homologous bZIP transcription factors of OsbZIP58. However, their function seems not to be fully in line with OsZIP58, and has divergent target genes and tissue dependence. ZmbZIP91 could bind to the ACTCAT directly to regulate the expression of AGPS1 , SSI , SSIIIa , and ISA1 during starch synthesis [9], while O2 [10] usually combines with other factors in the regulation of starch biosynthesis ( Figure 1 ).

Molecules 26 07092 g002 550
Figure 1. TF-regulating genes that encode starch biosynthetic enzymes. The formation of starch in cereal crops is the result of a series of enzymatic reactions, which require the cooperation of many TFs. Regulation of TFs on starch biosynthetic genes showed the following patterns: (i) the same gene was regulated by several TFs, i.e., GBSSI or Wx to RPBF, bZIP58, BP-5, and EBP-89, etc.; (ii) several genes were regulated by the same TF, i.e., ZmNAC128 and ZmNAC130; (iii) the regulation of TFs was also affected by various environments. Besides, there were regulatory differences of TFs in different cereals. For example, OsbZIP58 was close to ZmbZIP91 and O2, but their target genes were divergent.

Recently, a novel NAC-type transcription factor was revealed to regulate starch biosynthesis in wheat. TaNAC019 is specifically expressed in endosperm, and functions during starch synthesis through the following ways [11]: (i) by direct binding to the protomers of glutenin-encoded genes, (ii) by mediation of the accumulation of storage proteins via regulated Wheat storage protein activator ( TaSPA ) expression and interaction with TaGAMyb, and (iii) by adjustment of the accumulation of starch by the regulation of SSIIa and Susy1.

As the widely distributed transcription factors, MYBs are vital for a variety of biological functions. However, the functional studies of MYBs on starch biosynthesis are still scarce in cereal crops. So far, only one MYB factor has been reported as a regulator during starch biosynthesis [12].

GRAS transcription factors are involved in plant growth and development processes, especially for endodermis specification [13]. Besides, GRAS is greatly associated with type I genes during endosperm starch synthesis in rice [14], but its function as a regulator for starch biosynthesis is still not understood in cereal crops.

3. Other Regulators Directly Affecting Starch Biosynthesis

FLOURY ENDOSPREM is named based on its well-recognized but viable endosperm phenotypes, which usually display a chalky and soft endosperm. So far, 16 rice floury mutants [15] and three maize floury mutants [16] have been identified. However, only rice FLO2 [17] and FLO7 [18], as well as ZmFloury3 [16] serve as regulators of starch biosynthesis but do not act as enzymes. Although all of them play key roles in the regulation of starch formation, and are also responsible for aberrant seeds with reduced grain quality [16][17][18], their functioning models vary.

FLO2 acts as a regulatory protein that controls the biosynthesis of seed storage substances, possibly through its tetratricopeptide repeat (TPR) motifs for protein–protein interactions [17]. At least two proteins have been reported that interact with FLO2 during starch synthesis ( Figure 2 ). One basic helix–loop–helix (bHLH) protein may interact with FLO2 to modulate the expression of starch biosynthesis-associated nuclear genes (SBANGs) [17]. Subsequently, the FLO2-interacting cupin domain protein 1 (FLOC1) was reported to interact with the TPR motif of FLO2 to maintain fertility and seed quality in rice [19], even though they are supposed to have different functions.

Molecules 26 07092 g001 550
Figure 2. Overview of the regulators of starch metabolism in cereal crops. The figure was created based on the published literature (until 28 August 2021). The reported regulators and their target genes from different cereals were collected to build potential regulatory networks of starch metabolic genes. Starch biosynthesis involves a great deal of enzymatic and non-enzymatic proteins, which constitutes a very complex network. This process requires many regulators to match the providential functioning of these starch biosynthetic enzymes. Nowadays, dozens of transcription factors have been reported to directly regulate starch synthesis, i.e., bZIP58, NAC019, MYB14, FLO2, SUSIBA2, and so on. Besides, some regulators also control starch synthesis through the formation of proteins and sucrose, including MADS47, DOF1, and so on. Various regulators prefer to be activated in response to different fluctuating environments, such as hormone levels (i.e., ethylene, ETH; abscisic acid, ABA; gibberellin, GA), osmotic pressure (OP), sugar (i.e., sucrose, SUC), and high temperature (HT), etc. Regulators that exist in rice, maize, wheat, and barley are shown in blue, yellow, purple, and green color letters, respectively.

FLO7 prefers to specifically function in the endosperm periphery, and harbors two essential domains of an N -terminal transit peptide and an unknown function 1338 (DUF1338), during starch synthesis and amyloplast development [18].

The CRCT protein has been reported to be a regulator of starch biosynthesis in rice but does not seem to belong to a zinc finger motif [20], and cannot be listed in any of the above groups. Thus, here, CRCT is grouped independently. The expression of OsCRCT displays diurnal oscillation and is mainly focused on the vegetative organs. Therefore, OsCRCT serves as a positive regulator of several starch biosynthetic genes, including AGPS1 , AGPL1 , Glc-6-phosphate translocator2 ( GPT2 ) , plastidial α-glucan phosphorylase1 ( Pho1 ), and BEIIa , and contributes to starch biosynthesis in rice leaves [20]. The effects of OsCRCT on the storage of starch are unclear so far. However, the use of plants overexpressing OsCRCT is a potential approach to improve yields for food and biofuel [20], depending on the increased contents of starch derived from enhanced synthesis of starch instead of the defects of starch breakdown or translocation.

4. Regulators Indirectly Mediating Starch Biosynthesis

Aside from the direct regulators of starch biosynthesis, many other factors also participate in the regulation of starch synthesis, partially through the post-transcriptional regulation of TFs, i.e., micro RNAs (miRNAs), or via regulators of the formation of the upstream precursors and/or downstream products of starch.

Some transcription factors have been reported to mediate starch accumulation in cereal endosperms, but they participate in regulation via control of the synthesis of the downstream and/or upstream products of starch, i.e., sugar and proteins, instead of directly regulating starch synthesis. Here, we mainly concentrate on some of them ( Table 1 ), including bZIPs, NAC, DOF, MADS, and basic helix-loop-helix (bHLH).

Recently, one B3 domain-containing AP2/ERF transcriptional factor, ZmABI19 [21], was well documented to mediate starch synthesis via binding with RY through the regulation of cooperated expression of O2 , PBF1 , ZmbZIP22 , NAC130 , and O11 .

Regulation of NAC on starch synthetic enzymes is often accompanied with a simultaneous regulation of storage protein synthesis-associated genes ( Table 1 ). Although ZmNAC128 and ZmNAC130 have been well documented to regulate several starch biosynthetic genes, they can also bind with the motif of ACGCAA to activate the expression of 16-kDa γ-zein genes [22]. However, these two NAC factors [22] do not dimerize with each other but are functionally redundant for starch and protein accumulation. A similar phenomenon was also found in wheat [11]. TaNAC019 [11] has been reported to directly bind to the promoters of glutenin-encoded genes and be involved in the accumulation of starch and proteins. Therefore, the regulation of starch biosynthesis is not independent but prefers to act synergistically with other metabolic processes, i.e., protein synthesis.

Table 1. Regulators indirectly affecting starch biosynthesis of cereal crops.

TF Binding Domains Target Genes Specific Expressed Tissues References
Oryza sativa L.
RISBZ1/bZIP58 TCCACGT(a/c)R(a/t) and GATGYRTGG O2 Endosperm [23]
Zea mays L.
ZmbZIP22 ACAGCTCA 27-kDa γ-zein Endosperm [24]
O2 GA/TGAPyPuTGPu PPDK   [25][26][27]
O2 TCCACGTAGA 22 kDa zein All types of tissues [25][26][27]
OHP1 O2-likebox (TTTACGT) 27-kDa γ-zein and 22-kDa α-zein   [28]
OHP2 O2-likebox (TTTACGT) zein   [28]
ZmABI19 RY O2, PBF1, ZmbZIP22, NAC130, O11 Endosperm and embryo [21]
ZmNAC128 ACGCAA 16-kDa γ-zein Endosperm [22]
ZmNAC130 ACGCAA 16-kDa γ-zein Endosperm [22]
ZmMADS47 CATGT α-zein and 50-kDa γ-zein Endosperm [29]
PBF/DOF13 TGTAAAG 27-kD γ- and 22-kD α-zein Endosperm [10]
DOF1   γ-zein Endosperm [30]
Triticum aestivum L.
TaNAC019   SPA, GaMyb, Glutenin Endosperm [11]

References

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