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Review
. 2021 Dec 31;12(2):627-646.
doi: 10.1080/21645698.2021.1921545. Epub 2021 May 25.

Novel plant breeding techniques to advance nitrogen use efficiency in rice: A review

Affiliations
Review

Novel plant breeding techniques to advance nitrogen use efficiency in rice: A review

Sajid Fiaz et al. GM Crops Food. .

Abstract

Recently, there has been a remarkable increase in rice production owing to genetic improvement and increase in application of synthetic fertilizers. For sustainable agriculture, there is dire need to maintain a balance between profitability and input cost. To meet the steady growing demands of the farming community, researchers are utilizing all available resources to identify nutrient use efficient germplasm, but with very little success. Therefore, it is essential to understand the underlying genetic mechanism controlling nutrients efficiency, with the nitrogen use efficiency (NUE) being the most important trait. Information regarding genetic factors controlling nitrogen (N) transporters, assimilators, and remobilizers can help to identify candidate germplasms via high-throughput technologies. Large-scale field trials have provided morphological, physiological, and biochemical trait data for the detection of genomic regions controlling NUE. The functional aspects of these attributes are time-consuming, costly, labor-intensive, and less accurate. Therefore, the application of novel plant breeding techniques (NPBTs) with context to genome engineering has opened new avenues of research for crop improvement programs. Most recently, genome editing technologies (GETs) have undergone enormous development with various versions from Cas9, Cpf1, base, and prime editing. These GETs have been vigorously adapted in plant sciences for novel trait development to insure food quantity and quality. Base editing has been successfully applied to improve NUE in rice, demonstrating the potential of GETs to develop germplasms with improved resource use efficiency. NPBTs continue to face regulatory setbacks in some countries due to genome editing being categorized in the same category as genetically modified (GM) crops. Therefore, it is essential to involve all stakeholders in a detailed discussion on NPBTs and to formulate uniform policies tackling biosafety, social, ethical, and environmental concerns. In the current review, we have discussed the genetic mechanism of NUE and NPBTs for crop improvement programs with proof of concepts, transgenic and GET application for the development of NUE germplasms, and regulatory aspects of genome edited crops with future directions considering NUE.

Keywords: Green revolution; food security; genome engineering; resource use efficiency; synthetic fertilizers.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1.
Figure 1.
Illustration explaining various traits essential for the identification of NUE genotypes and different OMICS for the functional characterization of genes controlling NUE in rice.
Figure 2.
Figure 2.
Genes/Gene families involved in plant NUE (modified from.,
Figure 3.
Figure 3.
The basic flow chart of genome editing scheme for rice NUE improvement. (1) Selection of desirable germplasm. (2) The extraction of genomic DNA from selected germplasm. (3) Primarily analysis of genome through bioinformatics techniques to identify genes controlling NUE. (4) Selection of gene/genes of interest identified through bioinformatics analysis, available literature/online database. (5) Selection of target site based on GETs and availability/selection of vector. (6) Construction of vector holding gene of interest/target site. (7) Vector transformation through different transformation techniques (protoplast, agrobacterium transformation, and particle bombardment etc. (8) Utilization of Cas genome engineering machinery for targeted modification and extraction of genomic DNA from transgenic plants for mutation identification analysis. (9) The utilization of designed primers for PCR amplification of the target gene site to get Sanger sequencing results. (10) Screening of transgenic mutant plants based on Sanger sequencing results (type of mutation) and phenotypic changes. (11) Selection of transgene-free mutant plants for further collection of (morphological, physiological and biochemical) phenotypic data and interpretation of results.

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Grants and funding

The publication of the present work is supported by the National Key Research and Development Program of China (grant no. 2017YFC0504704) and the National Natural Science Foundation of China (51669034, 41761068, 51809224).

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