The discovery of the first yellow foliar mutation in soybean was not well-documented; however, by 1940 there were a few yellow foliar mutants known, which were described as yellow 1 (y1), y2, and so on (Morse and Cartter, 1937; Probst, 1950; Johnson and Bernard, 1962). Since then, many additional yellow foliar mutants have been identified in soybean.

Chlorophyll deficient mutants are broadly classified into two groups, viable-yellows and lethal-yellows. Viable-yellow mutant plants are capable of surviving with pale green or yellow/green leaves (Palmer et al., 2000; Sandhu et al., 2016) (Figure 1). As the seedlings grow, the plant may either outgrow the yellow leaves or retain the phenotype for the duration of its life depending on the mutated gene. Lethal-yellow mutant seedlings are initially yellow colored and have stunted growth, but are incapable of surviving. The plants vary in their length of survival from only for a few days after germination to a few weeks (Palmer et al., 2000; Sandhu et al., 2016).

Several mutants including y3, y11, y16, y18/y18_1, y18_2, y19, y21, yl_PR350, psbP, and CD-5 are considered lethal-yellows due to the early death of the plants (Table 1). One of the chlorophyll deficient mutant, y22, is considered conditional lethal as it produces seeds in a greenhouse; however, mutant plants die shortly after flowering in the field (Palmer et al., 1990). Y18-m was identified as an unstable mutable allele in soybean variety “Lincoln” that showed variegated yellow sectors of variable sizes (Peterson and Weber, 1969). Y18-m can change to stable forms Y18 or y18, or may remain unstable (Peterson and Weber, 1969) (Table 1). Inheritance study of two lethal-yellow mutants {T218H (y18) and T225H (y18_1)} from the progeny of Y18-m revealed that y18 and y18_1 were allelic (Kato and Palmer, 2004) (Table 1). The CD-5 and y11 mutants that exhibited similar phenotypes had identical amino acid substitution in paralogous genes (Campbell et al., 2015). Y11, Y18/Y18_1, Y18_2, YL_PR350, PsbP, and CD-5 were genetically mapped to chromosomes 13, 14, 17, 15, 3 and 15, respectively (Mahama et al., 2002; Kato and Palmer, 2004; Reed et al., 2014; Campbell et al., 2015; Sandhu et al., 2016).

The remaining 18 yellow mutants (y1, y4, y5, y6, y7, y8, y9, y10, y12, y13, y14, y17, y18-m, y20, y22, y23, tic110, and cd1) are viable (Table 1). Some mutants such as y6, y8, y10, and y13 develop yellow–green leaves in young plants but later stages develop more and more chlorophyll and become visually indistinguishable from normal green plants (Woodworth and Williams, 1938; Probst, 1950; Weiss, 1970b). On the contrary, the y23 mutant represents a weak plant which changes from green to yellow-white and slowly turns necrotic (Palmer et al., 1990). Y9, Y10, Y12, Y13, Y17, Y20, Y23, tic110, and Cd1 were genetically mapped to chromosomes 15, 3, 6, 13, 15, 12, 13, 2, and 10, respectively (Table 1).

Of 28 unique yellow foliar mutants known in soybean, 15 have been mapped to soybean chromosomes (Table 1). The genetic locations for the remaining 13 mutants are unknown.

A common characteristic of the yellow foliar mutants is a decrease in the total amount of chlorophyll which subsequently reduces photosynthetic activity. Chlorophyll synthesis is a multistep process that requires several enzymes (Johnson, 2016). Chlorophyllide esterification that is catalyzed by chlorophyll synthase is the last step in the chlorophyll biosynthesis process in plants. A missense mutation in the chlorophyll synthase gene that affected its enzyme activity resulted in yellow green leaf1 (ygl1) mutant in rice (Wu et al., 2007) (Figure 2). Protochlorophyllide oxidoreductase B (PORB) that is constitutively expressed throughout the leaf development is required for light dependent chlorophyll synthesis (Sakuraba et al., 2013). The faded green leaf (FGL) gene in rice encodes OsPORB, which catalyzes protochlorophyllide to chlorophyllide in chlorophyll synthesis (Sakuraba et al., 2013) (Figure 2). In the fgl mutant, the excessive accumulation of reactive oxygen species due to increased levels of non-photoactive protochlorophyllide led to the downregulation of the chlorophyll synthesis or photosynthesis related genes, resulting in the variegated leaf phenotype (Sakuraba et al., 2013). Magnesium chelatase that catalyzes the insertion of Mg²⁺ into the center of protoporphyrin IX contains three subunits (ChlH, ChlD, and ChlI) and is a key enzyme in chlorophyll biosynthesis (Johnson, 2016) (Figure 2). In rice, the yellow green leaf phenotype of the ygl7 mutant was due to a missense mutation in the gene encoding for magnesium-chelatase ChlD protein (Deng et al., 2014). Although, three additional yellow green rice mutants, chlorina-1, ygl98, and ygl3 display slightly different phenotypes, they represent different alleles of the ChlD gene (Deng et al., 2014) (Figure 2). Another rice mutant, chlorina-9, was shown to be the result of mutation in the gene encoding for ChlI subunit (Zhang et al., 2006). Similarly, two chlorophyll deficient phenotypes in soybean, y11 and CD-5, were due to mutations in paralogous genes encoding ChlI1a and ChlI1b (Campbell et al., 2015) (Figure 2).

In soybean, the majority of mutants cause a 30–66% reduction in overall chlorophyll content (Shoemaker et al., 1985; Zhang et al., 2011; Sandhu et al., 2016). Lethal-yellow mutants have considerably higher reduction in chlorophyll content as compared to viable-yellow mutants. For instance, chlorophyll content was reduced by ∼92% in the psbP (T378H) mutant (Sandhu et al., 2016). Nevertheless, the chlorophyll content of the mutants may not remain constant throughout the life cycle. Different mutants display diverse chlorophyll profiles during their development. For example, y3 showed higher chlorophyll content as compared to y11 at 35 days after planting; however, y3 showed less chlorophyll than y11 at 50 days after planting (Jiang et al., 1997).

In addition to the overall amount of chlorophyll, mutations also have an impact on the chlorophyll a/b ratio. Within each leaf there is a balance between the two different kinds of chlorophylls: chlorophyll a and chlorophyll b. Chlorophyll a is the most abundant pigment that absorbs wavelengths in the blue and red color range and Chlorophyll b primarily absorbs blue light. A mutation in OsCAO1 gene that encodes a chlorophyll a oxygenase, the enzyme responsible for the catalysis of chlorophyll a into chlorophyll b, was responsible for the pale green phenotype in rice (Lee et al., 2005) (Figure 2). In the majority of soybean mutants both types of chlorophylls have been reduced (Eskins and Banks, 1979; Eskins et al., 1983; Sandhu et al., 2016). However, when comparing the wild-type green and the yellow foliar mutants, the ratio of chlorophyll a/b was increased due to a more drastic decrease in chlorophyll b content then chlorophyll a (Shoemaker et al., 1985; Jiang et al., 1997; Zhang et al., 2011). Specifically, the y3, y7, y8, y9, y11, and cd1 mutants exhibited increased chlorophyll a/b ratio as compared to wild-type plant during leaf ontogeny (Eskins and Banks, 1979; Palmer et al., 1979; Eskins et al., 1983; Shoemaker et al., 1985; Ghirardi and Melis, 1988; Jiang et al., 1997; Zhang et al., 2011). Although, the majority of chlorophyll mutants displays an increased chlorophyll a/b ratio, however, some yellow foliar mutants (e.g., y18-m, psbP, and tic110) demonstrate no change in the chlorophyll a/b ratio (Cheng and Chandlee, 1999; Sandhu et al., 2016).

In addition to the synthesis, accumulation of chlorophyll is also very important in plants. The YLC1 (young leaf chlorosis 1) gene encodes DUF3353 family protein in rice that is targeted to chloroplast and is essential for chlorophyll and lutein accumulation during early leaf development (Zhou K. et al., 2013).

Chlorophylls are not the only photosynthetic pigments used by plants for photosynthesis; in fact there are typically several other pigments involved in photosynthetic process. Along with chlorophyll a and b there is lutein, carotene, violaxanthin, and neoxanthin (Eskins and Banks, 1979; Eskins et al., 1983). At least five soybean mutants (y3, y7, y8, y9, and y11) are known to directly impact the content of the other four photosynthetic pigments (Eskins and Banks, 1979; Eskins et al., 1983). All five mutants displayed decrease in the total amount of each pigment present in the leaves. Neoxanthin was drastically reduced while carotene, lutein, and violaxanthin were slightly reduced. Furthermore, the ratios of chlorophyll a to each pigment in the mutants, were distinctly different from the normal green soybean plant (Eskins et al., 1983). The ratio of chlorophyll a to neoxanthin amplifies significantly, whereas chlorophyll a to carotene, lutein, or violaxanthin ratios decrease.

The antennae are light harvesting complexes (LHCs) in chloroplast and are required for both photosystems to function properly. They are typically embedded into the thylakoid membranes. The LHCs absorb light energy and funnel it to the reaction center during photosynthesis. Certain mutations can actually decrease the size of the antennae which would affect the light harvesting capabilities of both photosystems. The y9 soybean mutant gene is a primary example of how photosynthesis is affected by reducing the amount of the LHC II polypeptides (Ghirardi and Melis, 1988). Overall the efficiency to undergo photosynthesis is decreased due to the reduction in available LHC II and the inability of LHC II to bind. At the same time the ratio between photosystem II (PSII) to photosystem I (PSI) have also been affected (Ghirardi and Melis, 1988). The mutants y3, y9, and y11 displayed increased relative ratio of PSII to PSI (Eskins et al., 1983). Due to this drastic increase, photosynthesis cannot function properly because there are not enough PSIs to take in the charged electrons from all of the PSIIs. Defects in biogenesis or assembly of photosystems often result in yellow mutants. For instance, for the YL_PR350 lethal-yellow mutant, a putative candidate gene was identified that codes for TAB2 protein known to play a role in biogenesis of photosystems I and II (Reed et al., 2014). Another lethal-yellow soybean mutant (T378H) was found to have a single base insertion in GmPsbP, an extrinsic protein of PSII which is critical for oxygen evolution during photosynthesis (Sandhu et al., 2016) (Figure 2). Reduction in photochemical conversion efficiency in psbP soybean mutant suggested damage to PSII (Sandhu et al., 2016). A stay-green mutant, in which chlorophyll degradation is impaired, is controlled by maternally inherited cytG gene that encodes the PsbM protein, an important component of the small subunits of PSII (Kohzuma et al., 2017). Interestingly, the y3 mutation that is nuclearly inherited is known to suppress the cytG phenotype (Kohzuma et al., 2017). The isolation and characterization of Y3 may shed light on underlying mechanism and the type of interaction between the Y3 and PsbM proteins.

The chloroplast is one of the most important organelles present in a plant and hosts the most complex and vital biochemical process, photosynthesis. The typical shape is either round or disk-shaped, but the shape of the chloroplast can vary. Of the known yellow foliar soybean mutants, some seem to display defects in chloroplast size and shape. Chloroplasts in the y11 mutant are around 6–8 μm in comparison to around 15 μm in a wild-type plant (Crang and Noble, 1974). The other mutant cd1 doesn’t show reduction in overall size; however, the chloroplasts are irregularly oval-shaped (Zhang et al., 2011). For the psbP mutant, proplastids were round and pyriformed with dense stroma and did not develop into normal chloroplast (Sandhu et al., 2016). The tic110 mutant displayed thinner and fewer chloroplasts with underdeveloped grana (Sandhu et al., 2016).

Thylakoids, the membranous structures present in the chloroplast, contain the pigments used in photosynthesis. In normal green soybean leaves, grana that are made of stacked thylakoids, contain anywhere from a few thylakoids to 10 or more. Grana are interconnected to one another via lamellae. Studies on different yellow foliar mutants revealed that the thylakoids and grana are commonly affected. Defects in two ATP dependent metelloproteases FtsH5 and FtsH2 that were shown to be involved in thylakoid membrane biogenesis in Arabidopsis resulted in variegated foliage mutants, var1 and var2, respectively (Sakamoto et al., 2002; Aluru et al., 2006). The lipid monogalactosyl diacylglycerol (MGD) and phosphatidyl glycerol phosphate (PGP) are two of the components of the thylakoid membranes that are important for their structural and functional integrity (Maréchal et al., 1997; Jarvis et al., 2000). Syntheses of MGD and PGP are catalyzed by MGD synthase and PGP synthase, respectively (Figure 2). Mutations in genes coding for these enzymes caused yellow–green mutants in Arabidopsis (Maréchal et al., 1997; Jarvis et al., 2000). Two rice yellow–green mutants, yl1 and ys83, that displayed problems in chloroplast development, were the results of mutation in a gene involved in biogenesis of chloroplast ATP synthase (cpATPase) (Chen et al., 2016; Ma et al., 2017) (Figure 2). Some proteins involved in signal transduction (UMP kinase), processing and stability of RNA (3-β-hydroxysterioid dehydrogenase/isomerase) and proteolysis (plastidic caseinolytic protease P6) have also been associated with chloroplast biogenesis and function in plants (Labesse et al., 2002; Dong et al., 2013; Shi et al., 2015; Zhu et al., 2016).

Some soybean mutants have less dense grana where only a few thylakoids are capable of attaching. For instance, in the y3, y9, y11, cd1 and psbP mutants, the thylakoids remain unstacked to form single stack grana (Wolf, 1963; Keck and Dilley, 1970; Crang and Noble, 1974; Palmer et al., 1979; Eskins et al., 1983; Shoemaker et al., 1985; Jiang et al., 1997; Zhang et al., 2011; Sandhu et al., 2016). Probably, when the plant is lacking certain functional proteins it leads to disrupted thylakoid stacking. Different yellow foliar mutants show subtle differences in thylakoid stacking and chloroplast development.

The Tic and Toc complexes are essential for proper chloroplast biogenesis as they are involved in the importing proteins from the cytosol (Bauer et al., 2000; Chen et al., 2002; Chou et al., 2003; Kovacheva et al., 2005; Kovacs-Bogdan et al., 2011). Defects in proteins involved in proper assembly of Tic and Toc complexes are known to be crucial for foliar pigmentation. In Arabidopsis the yellow foliar mutants, y2, y3, y4, and y19 that are incapable of producing large number of chloroplasts are tic20 mutants that contain decreased amounts of Tic20 mRNA (Chen et al., 2002). The thylakoid membranes were reduced, fewer thylakoids were capable of stacking into grana, and the sizes of the plastids were also reduced. The tic20 mutants also showed growth defects and were incapable of growing to their normal size (Kovacs-Bogdan et al., 2011). The reduction in Tic20 complexes also affected the import of three essential proteins for chloroplast: light-harvesting complex protein (LHCP), small subunit of ribulose-1,5-biphosphate carboxylase/oxygenase or RUBISCO (SSU), and α-subunit of the E1 subunit of pyruvate dehydrogenase (PDHα) (Chen et al., 2002). The total amounts of these proteins present within the chloroplasts were drastically reduced. Researchers argue that the reduction of the Tic20 complex is the main cause for the yellow phenotype and disruptions within the chloroplast (Chen et al., 2002; Kovacs-Bogdan et al., 2011) (Figure 2).

Independent knock out mutants of Tic40, Tic110, and Hsp90 complex genes in Arabidopsis were also explored for any developmental abnormalities (Kovacheva et al., 2005). The tic40 mutants developed the most severe chlorotic phenotype out of the three; in fact, the mutant plants had about 1/3 chlorophyll content as compared to the wild-types (Chou et al., 2003; Kovacheva et al., 2005) (Figure 2). Mesophyll cells of the plants lacking the Tic40 complex contained reduced number and smaller (45% smaller) chloroplasts, thylakoids were spherical and appeared swollen, reduced thylakoid membrane networks and a very few grana stacks present. The tic110 mutants are one of the few mutants that are lethal (Kovacheva et al., 2005). In addition, the mutants also showed retarded embryo development (delayed) compared to normal plants while very few embryos were capable of producing chloroplasts. Therefore, Tic110 is essential for embryo development and chloroplast biogenesis (Kovacheva et al., 2005; Kovacs-Bogdan et al., 2011). Phenotypically, the tic110 mutants were shorter and contained reduced chlorophyll levels with fewer thylakoids which resulted in yellowish leaves (Kovacs-Bogdan et al., 2011) (Figure 2). The hsp90 mutants did not depict severe phenotype but contained reduced chlorophyll and poorly developed chloroplasts (Kovacheva et al., 2005) (Figure 2). The protein importation capabilities of each complex were tested using 50S ribosomal subunits (L11) and RUBISCO proteins (SSU). The tic40 and hsp90 mutants had reduced importation of both proteins while tic110 presented subtle decreases (Kovacheva et al., 2005). In addition, tic40 also showed reduced importation of RuBP carboxylase, chlorophyll a/b binding protein (CAB), 33 kDa protein of oxygen-evolving complex (OE33) and POR (Chou et al., 2003). Hsp93 is known to interact with the import complex and may be critical of protein import (Kovacheva et al., 2005).

Toc complex, primarily made up of two GTP-regulated receptor proteins Toc34 and Toc159 along with a β-barrel membrane channel protein Toc75, recognizes and initiates the import of nuclear encoded proteins into the chloroplasts (Richardson et al., 2014). The ppi2 mutant which lacked the AtToc159 gene, developed a yellowish, pale phenotype with thylakoids that lacked membranes and starch granules (Bauer et al., 2000) (Figure 2). Protein import was also impacted by the lack of Toc159; two different proteins were employed to illustrate this effect. The toc159 mutant displayed reduction in importation of chlorophyll a/b binding protein and both the small and large subunits of RUBISCO (Bauer et al., 2000). The proplastids were unable to develop into mature chloroplasts.

As mentioned above, most of the research on Tic and Toc complexes has been done in Arabidopsis. It is likely that some of the yellow foliar mutants identified in soybean may be defective for Tic and Toc proteins. Recently, in a soybean viable-yellow mutant (T380), a single base deletion was observed in the Tic110 gene, causing a frameshift mutation that resulted in premature termination of encoded protein (Sandhu et al., 2016) (Figure 2). Future work on isolation of different soybean genes responsible for various yellow foliar mutants may shed light on the roles of different Tic and Toc proteins in soybean.

The components of electron transport system are directly involved in photosynthesis process in plants. Some mutants with defects in electron carrier proteins show yellow phenotypes. Electron acceptors are critical of energy generation process in an electron transport chain. A yellow–green mutant in rice, 501ys, was the result of missense mutation in the FdC2 gene that encodes ferredoxin-like protein (Li et al., 2015) (Figure 2). Ferredoxins are iron–sulfur proteins that are integral part of electron transport system in various metabolic pathways in a wide variety of organisms (Fukuyama, 2004). During photosynthesis, synthesis of NADPH via the electron transport system is an important step in plants. The knockout mutant of NAD kinase (nadk2) that catalyzes the de novo synthesis of NADP from NAD and ATP displayed reduced growth and pale yellow color in Arabidopsis (Chai et al., 2005) (Figure 2).

In soybean, extremely low F_v/F_m values in psbP indicated complete lack of electron transport activity (Sandhu et al., 2016). Similarly, in y11 mutant, the electron transport chain was shown to be defective (Keck et al., 1970). During photosynthesis, an electron acceptor, plastoquinone is reduced to plastoquinol and helps to transport the protons to the lumen of the thylakoids (Keck et al., 1970). The turnover rate for the oxidation of each plastoquinone molecule is drastically increased; which results in protons moving into the lumen faster (Keck et al., 1970). In addition, in the y11 mutant the plastoquinone pool is also enlarged. By combining these two factors the y11 yellow foliar mutant gene is capable of moving electrons faster than the wild-type soybean plant (Keck et al., 1970). The phenotype of such an increase results in light green leaves, reduced proteins, lower carotenoid values, decrease chlorophyll content, and altered thylakoid arrangements (Keck et al., 1970). Likewise, the defect in a chloroplast terminal oxidase that contains the ability to transfer electrons from the plastoquinol pool to oxygen resulted in green and white/yellow sectors in Arabidopsis leaves (Aluru et al., 2006).

The mutable gene Y18-m in soybean is considered unstable as it displays variegated yellow sectors on the leaves (Peterson and Weber, 1969; Palmer et al., 1979; Cheng, 1993; Kato and Palmer, 2004). The transition from Y18-m to y18 or Y18 is regulated by temperature (Palmer et al., 1979). This sensitivity to temperature caused a germinal mutation to occur within the reproductive cells of the plant (Cheng, 1993; Kato and Palmer, 2004). The heterozygous Y18-m y18 plants resulted into three different forms of gametes: Y18-m, Y18, and y18 in various ratios (Peterson and Weber, 1969; Palmer et al., 1979; Cheng, 1993). When the allele was mutated it is the offspring, not the parents, which were directly impacted by this mutated allele and displayed either a normal or yellow phenotype. The phenotype of the offspring was completely dependent on the plant growth temperature. If the yellow seedlings were grown at 29°C the mutant gene had a drastic impact on chloroplast content and development, and the grana and lamellar systems were disrupted (Palmer et al., 1979; Shoemaker et al., 1985). The chlorophyll content was reduced by half, but the ratio of chlorophyll a/b remained unchanged. If the yellow seedlings were grown at 19°C the thylakoid lumen fluctuated in size and there was an increase in the number of osmiophilic bodies present (Palmer et al., 1979). Therefore, the severity and hindrances produced within the chloroplast in yellow plants was completely dependent on what temperature the plants were grown at. Similarly, the chlorophyll deficient mutant, cde1, in rice was shown to be thermosensitive (Liu et al., 2007). The mutant showed normal phenotype at 23°C or lower, but at 26°C or higher the plant exhibited a yellow–green foliar phenotype. A glutamyl-tRNA synthase (OsGluRS) gene was shown to be responsible for this phenotype (Liu et al., 2007) (Figure 2). Certain yellow mutants showed the direct impact of illuminance on a soybean plant. A rice mutant light-induced yellow leaf1-1 (lyl1-1) was due to a mutation in geranylgeranyl reductase that is involved in reduction of Chl-geranylgeranylated (Chl_GG) and geranylgeranyl pyrophosphate (GGPP) to Chl-phytol (Chl_Phy) and phytyl pyrophosphate (PPP), resulting into defect in chlorophyll synthesis (Zhou Y. et al., 2013) (Figure 2). As LYL1 can be induced by light, it is believed to be critical in response to high light in rice (Zhou Y. et al., 2013). When exposed to high amounts of sunlight, the soybean mutants y11 and y18-m displayed absence of thylakoid stacking and lack of ribosomes in the stroma (Koller and Dilley, 1974; Palmer et al., 1979). In fact, the total amount of chlorophyll was reduced up to 10-fold with excessive illuminance (Koller and Dilley, 1974). Similar observations were made for the tic110 mutant where there were distinct phenotypic differences between the wild-type and the mutant at later growth stages under field conditions; however, phenotypes were indistinguishable in a greenhouse (Sandhu et al., 2016).

In several of the mutants, defects in some essential proteins may negatively impact photosynthesis. RUBISCO regulates photosynthesis by fixing carbon dioxide into energy-rich glucose molecules, which is found to be directly proportional to the photosynthetic rates of the plant (Johnson, 2016). In the fully expanded leaves of mutants y3 and y11, overall RUBISCO content was significantly reduced in comparison to the wild-type (Jiang et al., 1997). Other proteins that are affected in the y3 and y11 soybean mutants include CAB proteins (light harvesting chlorophyll a/b-binding proteins of PS II), RUBISCO activase, beta subunits of the chloroplast ATP synthase and cytochrome f. In y11, the RUBISCO activase, beta subunits and cytochrome f proteins decreased drastically throughout the leaf development; while the CAB proteins progressively increased over time (Jiang et al., 1997). The y3 mutant displayed a reduction in all four proteins listed above throughout the leaf development. The decline in these specific proteins negatively impacted the plant’s ability to undergo photosynthesis (Jiang et al., 1997).

The methylerythritol phosphate (MEP) pathway is involved in isoprenoid biosynthesis and is closely linked to photosynthesis as it uses its precursors and electrons from photosynthesis (Seemann et al., 2006). The methylerythritol 2,4-cyclodiphosphate synthase (IspF) gene was shown to be responsible for the yellow–green phenotype in rice mutant 505ys (Huang et al., 2018) (Figure 2). IspF catalyzes the conversion of 4-diphosphocytidyl-2-C-methyl-D-erythritol-2-phosphate (CDP-MEP) into 2-C-methyl-D-erythritol-2,4-cyclodiphosphate (ME-cPP) in the MEP pathway for isoprenoid biosynthesis (Herz et al., 2000).

Studies on light absorbance and utilization in soybean revealed that excessive chloroplast present in the top layer of leaves reduces the amount of sunlight that reaches the lower leaves (Pettigrew et al., 1989). The measurement of canopy photosynthetic CO₂-exchange rates (CER) determines how much photosynthetic proton flux density (PPFD) will pass through the leaves. If more PPFD is capable of passing through the chlorophyll-deficient leaves and reaches the lower leaves it will result in a higher overall CER value. The y9 and y11 mutants had up to 20 and 38% higher CER daily, respectively, compared to wild-types (Pettigrew et al., 1989). In a recent study performed in field conditions, decreased chlorophyll contents in y9 and y11 provided transient benefits by increasing leaf-level photosynthesis earlier in the growing season (Slattery et al., 2017). However, no improvement was seen in yield of mutant’s y9 and y11 in comparison to wild-type soybean, though these years were severely affected by drought (Slattery et al., 2017). Authors concluded that soybean plant overinvests in chlorophyll, as 50% reduction in chlorophyll did not significantly reduce yield and biomass accumulation; which means that relocation of nitrogen from pigment-protein complexes to other molecules involved in photosynthesis may be beneficial for plant productivity (Slattery et al., 2017). These conclusions are based on two mutants and single location. Multi-location trials including additional yellow mutants are necessary, which will provide definite conclusive evidence on the performance and yields of yellow mutants. Since, different mutants are operating in different pathways, a particular type of yellow mutant may be better than others in distributing light more proportionately in different leaf layers. Future studies targeting chlorophyll reduction and directing important resources toward increasing biochemical photosynthetic capacity are warranted to increase soybean productivity.

Insights from model systems can be invaluable in understanding mechanisms and pathways leading to yellow phenotypes in soybean. At least, 28 nuclearly inherited yellow foliar mutants have been identified in soybean, of which only four corresponding genes have been cloned. These include genes encoding for a magnesium-chelatase subunits ChlI1a and ChlI1b (Y11 and CD-5), translocon in the inner membrane of chloroplast (Tic110) and an extrinsic protein of PSII (PsbP) (Reed et al., 2014; Campbell et al., 2015; Sandhu et al., 2016) (Figure 2). Molecular and genetic research in model plants such as Arabidopsis and rice resulted in isolation and characterization of a number of genes associated with yellow phenotype. These include genes involved in chlorophyll biosynthesis, thylakoid biogenesis, lipid synthesis, RNA processing, proteolysis, transport proteins, components of electron transport chain, assembly and biogenesis of photosystems and signal transduction. Some of the characterized genes are associated with pathways seemingly distant from photosynthetic process. For example, the mutant IspF gene that is involved in isoprenoid synthesis through MEP pathway resulted in yellow phenotype in rice (Huang et al., 2018). Characterization of this gene established a link between photosynthesis and MEP pathway showing that photosynthesis is the source of electrons needed for the MEP pathway (Seemann et al., 2006) (Figure 2). The information generated for the isolated yellow foliar genes in plants clearly revealed that the structures and functions of various genes are conserved in different plant species. For instance, the rice yellow foliar mutant chlorina-9 is defective in magnesium chelatase subunit ChlI, homologs of which are shown to be responsible for the yellow green phenotype in two soybean mutants y11 and CD-5 (Zhang et al., 2006; Campbell et al., 2015) (Figure 2). Similarly, tic110 mutants display yellow foliar phenotypes in Arabidopsis and soybean (Sandhu et al., 2016). Likewise, the OsFdC2 gene in rice is also a functional ortholog of AtFdC2 (Li et al., 2015; Zhao et al., 2015) (Figure 2). As there are a number of yellow mutants identified in soybean, the homology based cloning approach will be highly effective in isolating and characterizing corresponding genes from soybean. The ease of transformation, availability of genetic resources, the body of information and availability of fully annotated genome makes Arabidopsis an ideal system to perform mechanistic studies on these genes. Lessons learnt from model plants can help in providing insights into the evolution of genetic networks involved in photosynthesis, a complex metabolic process vital for existence of plants. Characterization of yellow foliar mutants will provide effective means of understanding the modes of actions of proteins in metabolic pathways associated with foliage color in soybean. This, in turn, could explain the metabolic profiles of the sugar synthesis process in plants and facilitate in elaborating the underlying physiological and biochemical mechanisms. With the present attention and effort to understand the function of all genes in crop plants, the functional characterization of more genes involved in the yellow foliar phenotype may provide important tools to decipher connections between different metabolic pathways. As this has already been recognized that future gain in crop productivity will involve increasing efficiency of photosynthesis, the generation of new knowledge about the photosynthesis process will be the key to improved productivity of soybean and other crops in future.